Vaccine - Wikipedia

Vaccine - Wikipedia https://en.wikipedia.
org/wiki/Vaccine
Vaccine
A vaccine is a biological preparation that provides active
Vaccine
acquired immunity to a particular infectious disease.[1] A
vaccine typically contains an agent that resembles a
disease-causing microorganism and is oen made from
weakened or killed forms of the microbe, its toxins, or one
of its surface proteins. e agent stimulates the body's
immune system to recognize the agent as a threat, destroy
it, and to further recognize and destroy any of the
microorganisms associated with that agent that it may
encounter in the future. Vaccines can be prophylactic (to
prevent or ameliorate the effects of a future infection by a
natural or "wild" pathogen), or therapeutic (to fight a
Smallpox vaccine and equipment for
disease that has already occurred, such as cancer).[2][3][4][5]
administering it
e administration of vaccines is called vaccination. MeSH D014612
Vaccination is the most effective method of preventing
infectious diseases;[6] widespread immunity due to vaccination is largely responsible for the worldwide
eradication of smallpox and the restriction of diseases such as polio, measles, and tetanus from much of
the world. e effectiveness of vaccination has been widely studied and verified;[7] for example, vaccines
that have proven effective include the influenza vaccine,[8] the HPV vaccine,[9] and the chicken pox
vaccine.[10] e World Health Organization (WHO) reports that licensed vaccines are currently available
for twenty-five different preventable infections.[11]
e terms vaccine and vaccination are derived from Variolae vaccinae (smallpox of the cow), the term
devised by Edward Jenner (who both developed the concept of vaccines and created the first vaccine) to
denote cowpox. He used the phrase in 1798 for the long title of his Inquiry into the Variolae vaccinae
Known as the Cow Pox, in which he described the protective effect of cowpox against smallpox.[12] In 1881,
to honor Jenner, Louis Pasteur proposed that the terms should be extended to cover the new protective
inoculations then being developed.[13]
Contents
Effects
Adverse effects
Types
Inactivated
Attenuated
Toxoid
Subunit
Conjugate
Heterotypic
RNA
Experimental
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Vaccine - Wikipedia https://en.wikipedia.org/wiki/Vaccine
Valence
Other contents
Adjuvants
Preservatives
Excipients
Nomenclature
Licensure
World Health Organization
European Union
United States
Postmarketing surveillance
Schedule
Economics of development
Patents
Production
Vaccine manufacturers
Delivery systems
Veterinary medicine
DIVA vaccines
History
Generations of vaccines
Trends
Plants as bioreactors for vaccine production
See also
References
External links
Effects
ere is overwhelming scientific consensus that vaccines are a very safe and effective way to fight and
eradicate infectious diseases.[15][16][17][18] e immune system recognizes vaccine agents as foreign,
destroys them, and "remembers" them. When the virulent version of an agent is encountered, the body
recognizes the protein coat on the virus, and thus is prepared to respond, by first neutralizing the target
agent before it can enter cells, and secondly by recognizing and destroying infected cells before that agent
can multiply to vast numbers.
Limitations to their effectiveness, nevertheless, exist.[19] Sometimes, protection fails because of vaccine-
related failure such as failures in vaccine aenuation, vaccination regimes or administration or host-
related failure due to host's immune system simply does not respond adequately or at all. Lack of response
commonly results from genetics, immune status, age, health or nutritional status.[20] It also might fail for
genetic reasons if the host's immune system includes no strains of B cells that can generate antibodies
suited to reacting effectively and binding to the antigens associated with the pathogen.
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Even if the host does develop antibodies, protection might not be

adequate; immunity might develop too slowly to be effective in
time, the antibodies might not disable the pathogen completely, or
there might be multiple strains of the pathogen, not all of which are
equally susceptible to the immune reaction. However, even a
partial, late, or weak immunity, such as a one resulting from cross-
immunity to a strain other than the target strain, may mitigate an
infection, resulting in a lower mortality rate, lower morbidity, and
faster recovery.
Adjuvants commonly are used to boost immune response,

particularly for older people (50–75 years and up), whose immune
response to a simple vaccine may have weakened.[21]
e efficacy or performance of the vaccine is dependent on a

number of factors:
the disease itself (for some diseases vaccination

performs better than for others)
A child with measles, a vaccine-
the strain of vaccine (some vaccines are specific to, preventable disease[14]
or at least most effective against, particular strains
of the disease)[22]
whether the vaccination schedule has been properly observed.
idiosyncratic response to vaccination; some individuals are "non-responders" to
certain vaccines, meaning that they do not generate antibodies even after being
vaccinated correctly.
assorted factors such as ethnicity, age, or genetic predisposition.
If a vaccinated individual does develop the disease vaccinated against (breakthrough infection), the disease
is likely to be less virulent than in unvaccinated victims.[23]
e following are important considerations in the effectiveness of a vaccination program:[24]
1. careful modeling to anticipate the effect that an immunization campaign will have
on the epidemiology of the disease in the medium to long term
2. ongoing surveillance for the relevant disease following introduction of a new
vaccine
3. maintenance of high immunization rates, even when a disease has become rare.
In 1958, there were 763,094 cases of measles in the United States; 552 deaths resulted.[25][26] Aer the
introduction of new vaccines, the number of cases dropped to fewer than 150 per year (median of 56).[26]
In early 2008, there were 64 suspected cases of measles. Fiy-four of those infections were associated with
importation from another country, although only thirteen percent were actually acquired outside the
United States; 63 of the 64 individuals either had never been vaccinated against measles or were uncertain
whether they had been vaccinated.[26]
Vaccines led to the eradication of smallpox, one of the most contagious and deadly diseases in humans.[27]
Other diseases such as rubella, polio, measles, mumps, chickenpox, and typhoid are nowhere near as
common as they were a hundred years ago thanks to widespread vaccination programs. As long as the
vast majority of people are vaccinated, it is much more difficult for an outbreak of disease to occur, let
alone spread. is effect is called herd immunity. Polio, which is transmied only between humans, is
targeted by an extensive eradication campaign that has seen endemic polio restricted to only parts of three
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countries (Afghanistan, Nigeria, and Pakistan).[28] However, the difficulty of reaching all children as well
as cultural misunderstandings have caused the anticipated eradication date to be missed several times.
Vaccines also help prevent the development of antibiotic resistance. For example, by greatly reducing the
incidence of pneumonia caused by Streptococcus pneumoniae, vaccine programs have greatly reduced the
prevalence of infections resistant to penicillin or other first-line antibiotics.[29]
e measles vaccine is estimated to prevent a million deaths every year.[30]
Adverse effects
Vaccinations given to children, adolescents, or adults are generally safe.[31][32] Adverse effects, if any, are
generally mild.[33] e rate of side effects depends on the vaccine in question.[33] Some common side
effects include fever, pain around the injection site, and muscle aches.[33] Additionally, some individuals
may be allergic to ingredients in the vaccine.[34] MMR vaccine is rarely associated with febrile seizures.[32]
Host-("vaccinee")-related determinants that render a person susceptible to infection, such as genetics,

health status (underlying disease, nutrition, pregnancy, sensitivities or allergies), immune competence, age,
and economic impact or cultural environment can be primary or secondary factors affecting the severity
of infection and response to a vaccine.[35] Elderly (above age 60), allergen-hypersensitive, and obese
people have susceptibility to compromised immunogenicity, which prevents or inhibits vaccine
effectiveness, possibly requiring separate vaccine technologies for these specific populations or repetitive
booster vaccinations to limit virus transmission.[35]
Severe side effects are extremely rare.[32] Varicella vaccine is rarely associated with complications in
immunodeficient individuals, and rotavirus vaccines are moderately associated with intussusception.[32]
At least 19 countries have no-fault compensation programs to provide compensation for those suffering
severe adverse effects of vaccination.[36] e United States’ program is known as the National Childhood
Vaccine Injury Act, and the United Kingdom employs the Vaccine Damage Payment.
Types
Vaccines typically contain dead or inactivated organisms or
purified products derived from them.
ere are several types of vaccines in use.[37] ese represent

different strategies used to try to reduce the risk of illness while
retaining the ability to induce a beneficial immune response.
Inactivated
Some vaccines contain inactivated, but previously virulent, micro-

organisms that have been destroyed with chemicals, heat, or
radiation.[38] Examples include the IPV polio vaccine, hepatitis A
vaccine, rabies vaccine and most influenza vaccines.[39]
Vaccine
Attenuated
Some vaccines contain live, aenuated microorganisms. Many of these are active viruses that have been
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cultivated under conditions that disable their virulent

properties, or that use closely related but less
dangerous organisms to produce a broad immune
response. Although most aenuated vaccines are viral,
some are bacterial in nature. Examples include the viral
diseases yellow fever, measles, mumps, and rubella, and
the bacterial disease typhoid. e live Mycobacterium
tuberculosis vaccine developed by Calmee and Guérin
is not made of a contagious strain but contains a
virulently modified strain called "BCG" used to elicit an
immune response to the vaccine. e live aenuated
vaccine containing strain Yersinia pestis EV is used for
plague immunization. Aenuated vaccines have some
advantages and disadvantages. Aenuated, or live,
weakened, vaccines typically provoke more durable
immunological responses. But they may not be safe for
use in immunocompromised individuals, and on rare
occasions mutate to a virulent form and cause
disease.[40]
Avian flu vaccine development by reverse

Toxoid genetics techniques
Toxoid vaccines are made from inactivated toxic

compounds that cause illness rather than the micro-organism.[41] Examples of toxoid-based vaccines
include tetanus and diphtheria. Toxoid vaccines are known for their efficacy.[39] Not all toxoids are for
micro-organisms; for example, Crotalus atrox toxoid is used to vaccinate dogs against ralesnake bites.[42]
Subunit
Rather than introducing an inactivated or aenuated micro-organism to an immune system (which would
constitute a "whole-agent" vaccine), a subunit vaccine uses a fragment of it to create an immune response.
One example is the subunit vaccine against hepatitis B virus, that is composed of only the surface proteins
of the virus (previously extracted from the blood serum of chronically infected patients, but now produced
by recombination of the viral genes into yeast).[43] Another example is edible algae vaccines, such as the
virus-like particle (VLP) vaccine against human papillomavirus (HPV), which is composed of the viral
major capsid protein.[44] Another example is the hemagglutinin and neuraminidase subunits of the
influenza virus.[39] A subunit vaccine is being used for plague immunization.[45]
Conjugate
Certain bacteria have a polysaccharide outer coat that is poorly immunogenic. By linking these outer coats
to proteins (e.g., toxins), the immune system can be led to recognize the polysaccharide as if it were a
protein antigen. is approach is used in the Haemophilus influenzae type B vaccine.[46]
Heterotypic
Heterologous vaccines also known as "Jennerian vaccines", are vaccines that are pathogens of other
animals that either do not cause disease or cause mild disease in the organism being treated. e classic
example is Jenner's use of cowpox to protect against smallpox. A current example is the use of BCG
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vaccine made from Mycobacterium bovis to protect against tuberculosis.[47]
RNA
An mRNA vaccine (or RNA vaccine) is a novel type of vaccine which is composed of the nucleic acid RNA,
packaged within a vector such as lipid nanoparticles.[48] Among the COVID-19 vaccines are a number of
RNA vaccines under development to combat the COVID-19 pandemic and some have received emergency
use authorization in some countries. For example, the Pfizer and Moderna mRNA vaccines have
emergency use authorization in the US.[49][50][51]
Experimental
A number of innovative vaccines are also in development and in

use:
Dendritic cell vaccines combine dendritic cells with

antigens in order to present the antigens to the
body's white blood cells, thus stimulating an
immune reaction. These vaccines have shown some
positive preliminary results for treating brain
tumors [52] and are also tested in malignant
melanoma.[53]
DNA vaccination – The proposed mechanism is the
insertion and expression of viral or bacterial DNA in
human or animal cells (enhanced by the use of Electroporation system for
electroporation), triggering immune system experimental "DNA vaccine"
recognition. Some cells of the immune system that delivery
recognize the proteins expressed will mount an
attack against these proteins and cells expressing
them. Because these cells live for a very long time, if the pathogen that normally
expresses these proteins is encountered at a later time, they will be attacked
instantly by the immune system. One potential advantage of DNA vaccines is that
they are very easy to produce and store.
Recombinant vector – by combining the physiology of one micro-organism and the
DNA of another, immunity can be created against diseases that have complex
infection processes. An example is the RVSV-ZEBOV vaccine licensed to Merck that
is being used in 2018 to combat ebola in Congo.[54]
T-cell receptor peptide vaccines are under development for several diseases using
models of Valley Fever, stomatitis, and atopic dermatitis. These peptides have
been shown to modulate cytokine production and improve cell-mediated immunity.
Targeting of identified bacterial proteins that are involved in complement inhibition
would neutralize the key bacterial virulence mechanism. [55]
The use of plasmids has been validated in preclinical studies as a protective
vaccine strategy for cancer and infectious diseases. However, in human studies,
this approach has failed to provide clinically relevant benefit. The overall efficacy of
plasmid DNA immunization depends on increasing the plasmid's immunogenicity
while also correcting for factors involved in the specific activation of immune
effector cells.[56]
While most vaccines are created using inactivated or aenuated compounds from micro-organisms,
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synthetic vaccines are composed mainly or wholly of synthetic peptides, carbohydrates, or antigens.
Valence
Vaccines may be monovalent (also called univalent) or multivalent (also called polyvalent). A monovalent
vaccine is designed to immunize against a single antigen or single microorganism.[57] A multivalent or
polyvalent vaccine is designed to immunize against two or more strains of the same microorganism, or
against two or more microorganisms.[58] e valency of a multivalent vaccine may be denoted with a
Greek or Latin prefix (e.g., tetravalent or quadrivalent). In certain cases, a monovalent vaccine may be
preferable for rapidly developing a strong immune response.[59]
When two or more vaccines are mixed together in the same formulation, the two vaccines can interfere.
is most frequently occurs with live aenuated vaccines, where one of the vaccine components is more
robust than the others and suppresses the growth and immune response to the other components. is
phenomenon was first noted in the trivalent Sabin polio vaccine, where the amount of serotype 2 virus in
the vaccine had to be reduced to stop it from interfering with the "take" of the serotype 1 and 3 viruses in
the vaccine.[60] is phenomenon has also been found to be a problem with the dengue vaccines currently
being researched, where the DEN-3 serotype was found to predominate and suppress the response to
DEN-1, −2 and −4 serotypes.[61]
Other contents
Adjuvants
Vaccines typically contain one or more adjuvants, used to boost the immune response. Tetanus toxoid, for
instance, is usually adsorbed onto alum. is presents the antigen in such a way as to produce a greater
action than the simple aqueous tetanus toxoid. People who have an adverse reaction to adsorbed tetanus
toxoid may be given the simple vaccine when the time comes for a booster.[62]
In the preparation for the 1990 Persian Gulf campaign, whole cell pertussis vaccine was used as an
adjuvant for anthrax vaccine. is produces a more rapid immune response than giving only the anthrax
vaccine, which is of some benefit if exposure might be imminent.[63]
Preservatives
Vaccines may also contain preservatives to prevent contamination with bacteria or fungi. Until recent
years, the preservative thiomersal (A.K.A. imerosal in the US and Japan) was used in many vaccines that
did not contain live virus. As of 2005, the only childhood vaccine in the U.S. that contains thiomersal in
greater than trace amounts is the influenza vaccine,[64] which is currently recommended only for children
with certain risk factors.[65] Single-dose influenza vaccines supplied in the UK do not list thiomersal in the
ingredients. Preservatives may be used at various stages of production of vaccines, and the most
sophisticated methods of measurement might detect traces of them in the finished product, as they may in
the environment and population as a whole.[66]
Many vaccines need preservatives to prevent serious adverse effects such as Staphylococcus infection,
which in one 1928 incident killed 12 of 21 children inoculated with a diphtheria vaccine that lacked a
preservative.[67] Several preservatives are available, including thiomersal, phenoxyethanol, and
formaldehyde. iomersal is more effective against bacteria, has a beer shelf-life, and improves vaccine
stability, potency, and safety; but, in the U.S., the European Union, and a few other affluent countries, it is
no longer used as a preservative in childhood vaccines, as a precautionary measure due to its mercury
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content.[68] Although controversial claims have been made that thiomersal contributes to autism, no
convincing scientific evidence supports these claims.[69] Furthermore, a 10–11 year study of 657,461
children found that the MMR vaccine does not cause autism and actually reduced the risk of autism by
seven percent.[70][71]
Excipients
Beside the active vaccine itself, the following excipients and residual manufacturing compounds are
present or may be present in vaccine preparations:[72]
Aluminum salts or gels are added as adjuvants. Adjuvants are added to promote an
earlier, more potent response, and more persistent immune response to the
vaccine; they allow for a lower vaccine dosage.
Antibiotics are added to some vaccines to prevent the growth of bacteria during
production and storage of the vaccine.
Egg protein is present in the influenza vaccine and yellow fever vaccine as they are
prepared using chicken eggs. Other proteins may be present.
Formaldehyde is used to inactivate bacterial products for toxoid vaccines.
Formaldehyde is also used to inactivate unwanted viruses and kill bacteria that
might contaminate the vaccine during production.
Monosodium glutamate (MSG) and 2-phenoxyethanol are used as stabilizers in a
few vaccines to help the vaccine remain unchanged when the vaccine is exposed
to heat, light, acidity, or humidity.
Thiomersal is a mercury-containing antimicrobial that is added to vials of vaccine
that contain more than one dose to prevent contamination and growth of
potentially harmful bacteria. Due to the controversy surrounding thiomersal it has
been removed from most vaccines except multi-use influenza, where it was
reduced to levels so that a single dose contained less than a micro-gram of
mercury, a level similar to eating ten grams of canned tuna. [73]
Nomenclature
Various fairly standardized abbreviations for vaccine names have developed, although the standardization
is by no means centralized or global. For example, the vaccine names used in the United States have well-
established abbreviations that are also widely known and used elsewhere. An extensive list of them
provided in a sortable table and freely accessible, is available at a US Centers for Disease Control and
Prevention web page.[74] e page explains that "e abbreviations [in] this table (Column 3) were
standardized jointly by staff of the Centers for Disease Control and Prevention, ACIP Work Groups, the
editor of the Morbidity and Mortality Weekly Report (MMWR), the editor of Epidemiology and Prevention of
Vaccine-Preventable Diseases (the Pink Book), ACIP members, and liaison organizations to the ACIP."[74]
Some examples are "DTaP" for diphtheria and tetanus toxoids and acellular pertussis vaccine, "DT" for
diphtheria and tetanus toxoids, and "Td" for tetanus and diphtheria toxoids. At its page on tetanus
vaccination,[75] the CDC further explains that "Upper-case leers in these abbreviations denote full-
strength doses of diphtheria (D) and tetanus (T) toxoids and pertussis (P) vaccine. Lower-case "d" and "p"
denote reduced doses of diphtheria and pertussis used in the adolescent/adult-formulations. e 'a' in
DTaP and Tdap stands for 'acellular', meaning that the pertussis component contains only a part of the
pertussis organism."[75]
Another list of established vaccine abbreviations is at the CDC's page called "Vaccine Acronyms and
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Abbreviations", with abbreviations used on U.S. immunization records.[76] e United States Adopted
Name system has some conventions for the word order of vaccine names, placing head nouns first and
adjectives postpositively. is is why the USAN for "OPV" is "poliovirus vaccine live oral" rather than "oral
poliovirus vaccine".
Licensure
A vaccine licensure occurs aer the successful conclusion of the clinical trials program through Phases I–III
demonstrating safety, immunogenicity at a specific dose, effectiveness at preventing infection in target
populations, and enduring preventive effect.[77] As part of a multinational licensure for a vaccine, the
World Health Organization Expert Commiee on Biological Standardization developed guidelines of
international standards for manufacturing and quality control of vaccines, a process intended as a platform
for national regulatory agencies to apply for their own licensure process.[77] Vaccine manufacturers do not
receive licensure until a complete clinical package proves the vaccine is safe and has long-term
effectiveness, following scientific review by a multinational or national regulatory organization, such as
the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA).[78][79]
Upon developing countries adopting WHO guidelines for vaccine development and licensure, each
country has its own responsibility to issue a national licensure, and to manage, deploy, and monitor the
vaccine throughout its use in each nation.[77] Building trust and acceptance of a licensed vaccine among
the public is a task of communication by governments and healthcare personnel to ensure a vaccination
campaign proceeds smoothly, saves lives, and enables economic recovery.[80][81] When a vaccine is
licensed, it will initially be in limited supply due to variable manufacturing, distribution, and logistical
factors, requiring an allocation plan for the limited supply and which population segments should be
prioritized to first receive the vaccine.[80]
World Health Organization
Vaccines developed for multinational distribution via the United Nations Children's Fund (UNICEF)
require pre-qualification by the WHO to ensure international standards of quality, safety, immunogenicity,
and efficacy for adoption by numerous countries.[77]
e process requires manufacturing consistency at WHO-contracted laboratories following Good

Manufacturing Practice (GMP).[77] When UN agencies are involved in vaccine licensure, individual nations
collaborate by 1) issuing marketing authorization and a national license for the vaccine, its manufacturers,
and distribution partners; and 2) conducting postmarketing surveillance, including records for adverse
events aer the vaccination program. e WHO works with national agencies to monitor inspections of
manufacturing facilities and distributors for compliance with GMP and regulatory oversight.[77]
Some countries choose to buy vaccines licensed by reputable national organizations, such as EMA, FDA,
or national agencies in other affluent countries, but such purchases typically are more expensive and may
not have distribution resources suitable to local conditions in developing countries.[77]
European Union
In the European Union (EU), vaccines for pandemic pathogens, such as seasonal influenza, are licensed
EU-wide where all the member states comply ("centralized"), are licensed for only some member states
("decentralized"), or are licensed on an individual national level.[78] Generally, all EU states follow
regulatory guidance and clinical programs defined by the European Commiee for Medicinal Products for
Human Use (CHMP), a scientific panel of the European Medicines Agency (EMA) responsible for vaccine
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licensure.[78] e CHMP is supported by several expert groups who assess and monitor the progress of a
vaccine before and aer licensure and distribution.[78]
United States
Under the FDA, the process of establishing evidence for vaccine clinical safety and efficacy is the same as
for the approval process for prescription drugs.[82] If successful through the stages of clinical development,
the vaccine licensing process is followed by a Biologics License Application which must provide a
scientific review team (from diverse disciplines, such as physicians, statisticians, microbiologists, chemists)
a comprehensive documentation for the vaccine candidate having efficacy and safety throughout its
development. Also during this stage, the proposed manufacturing facility is examined by expert reviewers
for GMP compliance, and the label must have compliant description to enable health care providers
definition of vaccine specific use, including its possible risks, to communicate and deliver the vaccine to
the public.[82] Aer licensure, monitoring of the vaccine and its production, including periodic inspections
for GMP compliance, continue as long as the manufacturer retains its license, which may include
additional submissions to the FDA of tests for potency, safety, and purity for each vaccine manufacturing
step.[82]
Postmarketing surveillance
Until a vaccine is in use for the general population, all potential adverse events from the vaccine may not
be known, requiring manufacturers to conduct Phase IV studies for postmarketing surveillance of the
vaccine while it is used widely in the public.[77][82] e WHO works with UN member states to implement
postlicensing surveillance.[77] e FDA relies on a Vaccine Adverse Event Reporting System to monitor
safety concerns about a vaccine throughout its use in the American public.[82]
Schedule
In order to provide the best protection, children
are recommended to receive vaccinations as
soon as their immune systems are sufficiently
developed to respond to particular vaccines,
with additional "booster" shots oen required
to achieve "full immunity". is has led to the
development of complex vaccination schedules.
In the United States, the Advisory Commiee
on Immunization Practices, which recommends
schedule additions for the Centers for Disease
Control and Prevention, recommends routine
vaccination of children against[83] hepatitis A,
hepatitis B, polio, mumps, measles, rubella,
diphtheria, pertussis, tetanus, HiB, chickenpox,
rotavirus, influenza, meningococcal disease and
pneumonia.[84]
e large number of vaccines and boosters recommended (up to 24 injections by age two) has led to
problems with achieving full compliance. In order to combat declining compliance rates, various
notification systems have been instituted and a number of combination injections are now marketed (e.g.,
Pneumococcal conjugate vaccine and MMRV vaccine), which provide protection against multiple diseases.
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Besides recommendations for infant vaccinations and boosters, many specific vaccines are recommended
for other ages or for repeated injections throughout life – most commonly for measles, tetanus, influenza,
and pneumonia. Pregnant women are oen screened for continued resistance to rubella. e human
papillomavirus vaccine is recommended in the U.S. (as of 2011)[85] and UK (as of 2009).[86] Vaccine
recommendations for the elderly concentrate on pneumonia and influenza, which are more deadly to that
group. In 2006, a vaccine was introduced against shingles, a disease caused by the chickenpox virus, which
usually affects the elderly.
Economics of development
One challenge in vaccine development is economic: Many of the diseases most demanding a vaccine,
including HIV, malaria and tuberculosis, exist principally in poor countries. Pharmaceutical firms and
biotechnology companies have lile incentive to develop vaccines for these diseases because there is lile
revenue potential. Even in more affluent countries, financial returns are usually minimal and the financial
and other risks are great.[87]
Most vaccine development to date has relied on "push" funding by government, universities and non-profit
organizations.[88] Many vaccines have been highly cost effective and beneficial for public health.[89] e
number of vaccines actually administered has risen dramatically in recent decades.[90] is increase,
particularly in the number of different vaccines administered to children before entry into schools may be
due to government mandates and support, rather than economic incentive.[91]
Patents
e filing of patents on vaccine development processes can also be viewed as an obstacle to the
development of new vaccines. Because of the weak protection offered through a patent on the final
product, the protection of the innovation regarding vaccines is oen made through the patent of processes
used in the development of new vaccines as well as the protection of secrecy.[92]
According to the World Health Organization, the biggest barrier to local vaccine production in less
developed countries has not been patents, but the substantial financial, infrastructure, and workforce
expertise requirements needed for market entry. Vaccines are complex mixtures of biological compounds,
and unlike the case of drugs, there are no true generic vaccines. e vaccine produced by a new facility
must undergo complete clinical testing for safety and efficacy similar to that undergone by that produced
by the original manufacturer. For most vaccines, specific processes have been patented. ese can be
circumvented by alternative manufacturing methods, but this required R&D infrastructure and a suitably
skilled workforce. In the case of a few relatively new vaccines such as the human papillomavirus vaccine,
the patents may impose an additional barrier.[93]
Production
Vaccine production has several stages. First, the antigen itself is
generated. Viruses are grown either on primary cells such as
chicken eggs (e.g., for influenza) or on continuous cell lines such as
cultured human cells (e.g., for hepatitis A).[94] Bacteria are grown in
bioreactors (e.g., Haemophilus influenzae type b). Likewise, a
recombinant protein derived from the viruses or bacteria can be
generated in yeast, bacteria, or cell cultures.[95][96]
Aer the antigen is generated, it is isolated from the cells used to

generate it. A virus may need to be inactivated, possibly with no
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further purification required. Recombinant proteins need many operations involving ultrafiltration and
column chromatography. Finally, the vaccine is formulated by adding adjuvant, stabilizers, and
preservatives as needed. e adjuvant enhances the immune response to the antigen, stabilizers increase
the storage life, and preservatives allow the use of multidose vials.[95][96] Combination vaccines are harder
to develop and produce, because of potential incompatibilities and interactions among the antigens and
other ingredients involved.[97]
e final stage in vaccine manufacture before distribution is fill and finish, which is the process of filling
vials with vaccines and packaging them for distribution. Although this is a conceptually simple part of the
vaccine manufacture process, it is oen a boleneck in the process of distributing and administering
vaccines.[98][99][100]
Vaccine production techniques are evolving. Cultured mammalian cells are expected to become
increasingly important, compared to conventional options such as chicken eggs, due to greater
productivity and low incidence of problems with contamination. Recombination technology that produces
genetically detoxified vaccine is expected to grow in popularity for the production of bacterial vaccines
that use toxoids. Combination vaccines are expected to reduce the quantities of antigens they contain, and
thereby decrease undesirable interactions, by using pathogen-associated molecular paerns.[97]
Vaccine manufacturers
In 2012 the increasing role of Indian and Chinese vaccine manufacturers in meeting the global demand for
vaccine doses was noted.[101] e Serum Institute of India was at that point the world's largest
manufacturer of vaccines against measles and rubella, as well as combination DTP vaccines. e Serum
Institute of India made a name for itself as developer of vaccines when it brought into production its
measles vaccine using a MRC-5 cell culture instead of chicken eggs, allowing for a productivity increase at
10% to 20% compared to Merck Group and GlaxoSmithKline. In 2012 it was estimated that two out of three
vaccinated children globally had been immunized using a vaccine manufactured by the Serum Institute of
India. In 2012 China ranked as the largest vaccine manufacturing country in the world, with 46 registered
vaccine manufacturers focusing on meeting China's domestic need for vaccine doses. 90% of doses for the
Chinese National Immunization Program were supplied by the state-owned China National
Pharmaceutical Group.[102]
Delivery systems
One of the most common methods of delivering vaccines into the
human body is injection.
e development of new delivery systems raises the hope of

vaccines that are safer and more efficient to deliver and administer.
Lines of research include liposomes and ISCOM (immune
stimulating complex).[103]
Notable developments in vaccine delivery technologies have

included oral vaccines. Early aempts to apply oral vaccines
showed varying degrees of promise, beginning early in the 20th
century, at a time when the very possibility of an effective oral antibacterial vaccine was controversial.[104]
By the 1930s there was increasing interest in the prophylactic value of an oral typhoid fever vaccine for
example.[105]
An oral polio vaccine turned out to be effective when vaccinations were administered by volunteer staff
without formal training; the results also demonstrated increased ease and efficiency of administering the
12 of 31 13/03/2021, 13:32
vaccines. Effective oral vaccines have many advantages; for example, there is no risk of blood
contamination. Vaccines intended for oral administration need not be liquid, and as solids, they commonly
are more stable and less prone to damage or to spoilage by freezing in transport and storage.[106] Such
stability reduces the need for a "cold chain": the resources required to keep vaccines within a restricted
temperature range from the manufacturing stage to the point of administration, which, in turn, may
decrease costs of vaccines.
A microneedle approach, which is still in stages of development, uses "pointed projections fabricated into
arrays that can create vaccine delivery pathways through the skin".[107]
An experimental needle-free[108] vaccine delivery system is undergoing animal testing.[109][110] A stamp-

size patch similar to an adhesive bandage contains about 20,000 microscopic projections per square
cm.[111] is dermal administration potentially increases the effectiveness of vaccination, while requiring
less vaccine than injection.[112]
Veterinary medicine
Vaccinations of animals are used both to prevent their contracting
diseases and to prevent transmission of disease to humans.[113] Both
animals kept as pets and animals raised as livestock are routinely
vaccinated. In some instances, wild populations may be vaccinated.
is is sometimes accomplished with vaccine-laced food spread in a
disease-prone area and has been used to aempt to control rabies in
raccoons.
Where rabies occurs, rabies vaccination of dogs may be required by

law. Other canine vaccines include canine distemper, canine Goat vaccination against
parvovirus, infectious canine hepatitis, adenovirus-2, leptospirosis, sheep pox and pleural
Bordetella, canine parainfluenza virus, and Lyme disease, among pneumonia
others.
Cases of veterinary vaccines used in humans have been documented, whether intentional or accidental,
with some cases of resultant illness, most notably with brucellosis.[114] However, the reporting of such
cases is rare and very lile has been studied about the safety and results of such practices. With the advent
of aerosol vaccination in veterinary clinics, human exposure to pathogens that are not naturally carried in
humans, such as Bordetella bronchiseptica, has likely increased in recent years.[114] In some cases, most
notably rabies, the parallel veterinary vaccine against a pathogen may be as much as orders of magnitude
more economical than the human one.
DIVA vaccines
DIVA (Differentiation of Infected from Vaccinated Animals), also known as SIVA (Segregation of Infected
from Vaccinated Animals) vaccines, make it possible to differentiate between infected and vaccinated
animals. DIVA vaccines carry at least one epitope less than the equivalent wild microorganism. An
accompanying diagnostic test that detects the antibody against that epitope assists in identifying whether
the animal has been vaccinated or not.
e first DIVA vaccines (formerly termed marker vaccines and since 1999 coined as DIVA vaccines) and
companion diagnostic tests were developed by J. T. van Oirschot and colleagues at the Central Veterinary
Institute in Lelystad, e Netherlands.[115][116] ey found that some existing vaccines against
pseudorabies (also termed Aujeszky's disease) had deletions in their viral genome (among which was the
gE gene). Monoclonal antibodies were produced against that deletion and selected to develop an ELISA
13 of 31 13/03/2021, 13:32
that demonstrated antibodies against gE. In addition, novel genetically engineered gE-negative vaccines
were constructed.[117] Along the same lines, DIVA vaccines and companion diagnostic tests against bovine
herpesvirus 1 infections have been developed.[116][118]
e DIVA strategy has been applied in various countries to successfully eradicate pseudorabies virus from
those countries. Swine populations were intensively vaccinated and monitored by the companion
diagnostic test and, subsequently, the infected pigs were removed from the population. Bovine
herpesvirus 1 DIVA vaccines are also widely used in practice. Considerable efforts are ongoing to apply
the DIVA principle to a wide range of infectious diseases, such as classical swine fever,[119] avian
influenza,[120] Actinobacillus pleuropneumonia[121] and Salmonella infections in pigs.[122]
History
Prior to the introduction of vaccination with material from cases of
cowpox (heterotypic immunisation), smallpox could be prevented
by deliberate variolation with smallpox virus. e earliest hints of
the practice of variolation for smallpox in China come during the
10th century.[123] e Chinese also practiced the oldest documented
use of variolation, dating back to the fieenth century. ey
implemented a method of "nasal insufflation" administered by
blowing powdered smallpox material, usually scabs, up the nostrils. Comparison of smallpox (left)
Various insufflation techniques have been recorded throughout the and cowpox inoculations 16
sixteenth and seventeenth centuries within China.[124]:60 Two days after administration
reports on the Chinese practice of inoculation were received by the (1802)
Royal Society in London in 1700; one by Martin Lister who received
a report by an employee of the East India Company stationed in
China and another by Clopton Havers.[125]
Mary Wortley Montagu, who had witnessed variolation in Turkey,

had her four-year-old daughter variolated in the presence of
physicians of the Royal Court in 1721 upon her return to
England.[124] Later on that year Charles Maitland conducted an
experimental variolation of six prisoners in Newgate Prison in
London.[126] e experiment was a success, and soon variolation
was drawing aention from the royal family, who helped promote
the procedure. However, several days aer Prince Octavius of Great
Britain was inoculated he died in 1783.[127] In 1796 the physician
Edward Jenner took pus from the hand of a milkmaid with cowpox,
scratched it into the arm of an 8-year-old boy, James Phipps, and
six weeks later variolated the boy with smallpox, aerwards observing that he did not catch smallpox.
[128][129] Jenner extended his studies and in 1798 reported that his vaccine was safe in children and adults
and could be transferred from arm-to-arm reducing reliance on uncertain supplies from infected cows.[130]
Since vaccination with cowpox was much safer than smallpox inoculation,[131] the laer, though still
widely practiced in England, was banned in 1840.[132]
Following on from Jenner's work, the second generation of vaccines was introduced in the 1880s by Louis
Pasteur who developed vaccines for chicken cholera and anthrax,[13] and from the late nineteenth century
vaccines were considered a maer of national prestige. National vaccination policies were adopted and
compulsory vaccination laws were passed.[128] In 1931 Alice Miles Woodruff and Ernest Goodpasture
documented that the fowlpox virus could be grown in embryonated chicken egg. Soon scientist cultivated
other viruses in eggs. Eggs were used for virus propagation in the development of a yellow fever vaccine
in 1935 and a influenza vaccine in 1945. In 1959 growth media and cell culture replaced eggs as the
14 of 31 13/03/2021, 13:32
standard method of virus propagation for vaccines.[133]
e twentieth century saw the introduction of several successful

vaccines, including those against diphtheria, measles, mumps, and
rubella. Major achievements included the development of the polio
vaccine in the 1950s and the eradication of smallpox during the
1960s and 1970s. Maurice Hilleman was the most prolific of the
developers of the vaccines in the twentieth century. As vaccines
became more common, many people began taking them for
granted. However, vaccines remain elusive for many important French print in 1896 marking
diseases, including herpes simplex, malaria, gonorrhea, and the centenary of Jenner's
HIV.[128][134] vaccine
Generations of vaccines
First generation vaccines are whole-organism vaccines – either live

and weakened, or killed forms.[135] Live, aenuated vaccines, such
as smallpox and polio vaccines, are able to induce killer T-cell (TC
or CTL) responses, helper T-cell (TH) responses and antibody
immunity. However, aenuated forms of a pathogen can convert to
a dangerous form and may cause disease in immunocompromised
vaccine recipients (such as those with AIDS). While killed vaccines
do not have this risk, they cannot generate specific killer T cell Vials of an anthrax vaccine and
responses and may not work at all for some diseases.[135] a smallpox vaccine
Second generation vaccines were developed to reduce the risks

from live vaccines. ese are subunit vaccines, consisting of specific protein antigens (such as tetanus or
diphtheria toxoid) or recombinant protein components (such as the hepatitis B surface antigen). ey can
generate TH and antibody responses, but not killer T cell responses.
RNA vaccines and DNA vaccines are examples of third generation vaccines.[135][136][137] In 2016 a DNA
vaccine for the Zika virus began testing at the National Institutes of Health. Separately, Inovio
Pharmaceuticals and GeneOne Life Science began tests of a different DNA vaccine against Zika in Miami.
Manufacturing the vaccines in volume was unsolved as of 2016.[138] Clinical trials for DNA vaccines to
prevent HIV are underway.[139] mRNA vaccines such as BNT162b2 were developed in the year 2020 with
the help of Operation Warp Speed and massively deployed to combat the coronavirus pandemic.
Trends
Since at least 2013, scientists were trying to develop synthetic 3rd-generation vaccines by reconstructing
the outside structure of a virus; it was hoped that this will help prevent vaccine resistance.[140]
Principles that govern the immune response can now be used in tailor-made vaccines against many
noninfectious human diseases, such as cancers and autoimmune disorders.[141] For example, the
experimental vaccine CYT006-AngQb has been investigated as a possible treatment for high blood
pressure.[142] Factors that affect the trends of vaccine development include progress in translatory
medicine, demographics, regulatory science, political, cultural, and social responses.[143]
Plants as bioreactors for vaccine production
e idea of vaccine production via transgenic plants was identified as early as 2003. Plants such as tobacco,
15 of 31 13/03/2021, 13:32
potato, tomato, and banana can have genes inserted that cause them to produce vaccines usable for
humans.[144] In 2005, bananas were developed that produce a human vaccine against hepatitis B.[145]
Another example is the expression of a fusion protein in alfalfa transgenic plants for the selective
directioning to antigen presenting cells, therefore increasing vaccine potency against Bovine Viral
Diarrhea Virus (BVDV).[146][147]
See also
Biologics Control Act
Coalition for Epidemic Preparedness Innovations
Flying syringe
Immunization registry
Immunotherapy
List of vaccine ingredients
List of vaccine topics
Non-specific effect of vaccines
OPV AIDS hypothesis
Preventive healthcare
Reverse vaccinology
TA-CD
Timeline of vaccines
Virosome
Vaccine adverse event (safety issues)
Vaccine cooler
Vaccine failure
Vaccine hesitancy
Vaccinov
Viral vector
Virus-like particle
References
1. "Expanded Practice Standards" (https://www.legis.iowa.gov/docs/iac/rule/657.39.1
1.pdf) (PDF). Iowa Administrative Code. 2019.
2. Melief CJ, van Hall T, Arens R, Ossendorp F, van der Burg SH (September 2015).
"Therapeutic cancer vaccines" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC458
8240). The Journal of Clinical Investigation. 125 (9): 3401–12.
doi:10.1172/JCI80009 (https://doi.org/10.1172%2FJCI80009). PMC 4588240 (https://
www.ncbi.nlm.nih.gov/pmc/articles/PMC4588240). PMID 26214521 (https://pubme
d.ncbi.nlm.nih.gov/26214521).
16 of 31 13/03/2021, 13:32
3. Bol KF, Aarntzen EH, Pots JM, Olde Nordkamp MA, van de Rakt MW, Scharenborg
NM, de Boer AJ, van Oorschot TG, Croockewit SA, Blokx WA, Oyen WJ, Boerman OC,
Mus RD, van Rossum MM, van der Graaf CA, Punt CJ, Adema GJ, Figdor CG, de Vries
IJ, Schreibelt G (March 2016). "Prophylactic vaccines are potent activators of
monocyte-derived dendritic cells and drive effective anti-tumor responses in
melanoma patients at the cost of toxicity" (https://www.ncbi.nlm.nih.gov/pmc/articl
es/PMC4779136). Cancer Immunology, Immunotherapy. 65 (3): 327–39.
doi:10.1007/s00262-016-1796-7 (https://doi.org/10.1007%2Fs00262-016-1796-7).
PMC 4779136 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779136).
PMID 26861670 (https://pubmed.ncbi.nlm.nih.gov/26861670).
4. Brotherton J (2015). "HPV prophylactic vaccines: lessons learned from 10 years
experience". Future Virology. 10 (8): 999–1009. doi:10.2217/fvl.15.60 (https://doi.o
rg/10.2217%2Ffvl.15.60).
5. Frazer IH (May 2014). "Development and implementation of papillomavirus
prophylactic vaccines" (https://doi.org/10.4049%2Fjimmunol.1490012). Journal of
Immunology. 192 (9): 4007–11. doi:10.4049/jimmunol.1490012 (https://doi.org/10.
4049%2Fjimmunol.1490012). PMID 24748633 (https://pubmed.ncbi.nlm.nih.gov/24
748633).
6. *United States Centers for Disease Control and Prevention (2011). A CDC
framework for preventing infectious diseases. (https://www.cdc.gov/oid/docs/ID-Fra
mework.pdf) Archived (https://web.archive.org/web/20170829133723/https://www.
cdc.gov/oid/docs/ID-Framework.pdf) 2017-08-29 at the Wayback Machine Accessed
11 September 2012. "Vaccines are our most effective and cost-saving tools for
disease prevention, preventing untold suffering and saving tens of thousands of
lives and billions of dollars in healthcare costs each year."
American Medical Association (2000). Vaccines and infectious diseases: putting
risk into perspective. (http://www.immunizationinfo.org/es/pressroom/2000-06-0
1/vaccines-and-infectious-diseases-putting-risk-perspective) Archived (https://w
eb.archive.org/web/20150205193837/http://www.immunizationinfo.org/es/pressr
oom/2000-06-01/vaccines-and-infectious-diseases-putting-risk-perspective)
2015-02-05 at the Wayback Machine Accessed 11 September 2012. "Vaccines
are the most effective public health tool ever created."
Public Health Agency of Canada. Vaccine-preventable diseases. (http://www.pha
c-aspc.gc.ca/im/vpd-mev/index-eng.php) Archived (https://web.archive.org/web/
20150313131826/http://www.phac-aspc.gc.ca/im/vpd-mev/index-eng.php)
2015-03-13 at the Wayback Machine Accessed 11 September 2012. "Vaccines
still provide the most effective, longest-lasting method of preventing infectious
diseases in all age groups."
United States National Institute of Allergy and Infectious Diseases (NIAID). NIAID
Biodefense Research Agenda for Category B and C Priority Pathogens. (http://vir
tualbiosecuritycenter.org/wp-content/uploads/2012/01/Library-NIAID-Biodefense-
Research-Agenda-for-Category-B-and-C-Priority-Pathogens.pdf) Archived (https://
web.archive.org/web/20160304065419/http://virtualbiosecuritycenter.org/wp-co
ntent/uploads/2012/01/Library-NIAID-Biodefense-Research-Agenda-for-Category-
B-and-C-Priority-Pathogens.pdf) 2016-03-04 at the Wayback Machine Accessed
11 September 2012. "Vaccines are the most effective method of protecting the
public against infectious diseases."
7. Zimmer, Carl (20 November 2020). "2 Companies Say Their Vaccines Are 95%
Effective. What Does That Mean? You might assume that 95 out of every 100
people vaccinated will be protected from Covid-19. But that's not how the math
works" (https://www.nytimes.com/2020/11/20/health/covid-vaccine-95-effective.ht
ml). The New York Times. Retrieved 21 November 2020.
17 of 31 13/03/2021, 13:32
8. Fiore AE, Bridges CB, Cox NJ (2009). "Seasonal influenza vaccines". Vaccines for
Pandemic Influenza. Curr. Top. Microbiol. Immunol. Current Topics in Microbiology
and Immunology. 333. pp. 43–82. doi:10.1007/978-3-540-92165-3_3 (https://doi.or
g/10.1007%2F978-3-540-92165-3_3). ISBN 978-3-540-92164-6. PMID 19768400 (ht
tps://pubmed.ncbi.nlm.nih.gov/19768400).
9. Chang Y, Brewer NT, Rinas AC, Schmitt K, Smith JS (July 2009). "Evaluating the
impact of human papillomavirus vaccines". Vaccine. 27 (32): 4355–62.
doi:10.1016/j.vaccine.2009.03.008 (https://doi.org/10.1016%2Fj.vaccine.2009.03.0
08). PMID 19515467 (https://pubmed.ncbi.nlm.nih.gov/19515467).
10. Liesegang TJ (August 2009). "Varicella zoster virus vaccines: effective, but concerns
linger" (https://semanticscholar.org/paper/7a8870d019b79f046138cca99b6301e9fc
d9d4d1). Canadian Journal of Ophthalmology. 44 (4): 379–84. doi:10.3129/i09-126
(https://doi.org/10.3129%2Fi09-126). PMID 19606157 (https://pubmed.ncbi.nlm.nih.
gov/19606157). S2CID 662998 (https://api.semanticscholar.org/CorpusID:662998).
11. World Health Organization, Global Vaccine Action Plan 2011-2020. (https://www.wh
o.int/immunization/global_vaccine_action_plan/GVAP_doc_2011_2020/en/) Archived
(https://web.archive.org/web/20140414035449/http://www.who.int/immunization/gl
obal_vaccine_action_plan/GVAP_doc_2011_2020/en/) 2014-04-14 at the Wayback
Machine Geneva, 2012.
12. Baxby D (January 1999). "Edward Jenner's Inquiry; a bicentenary analysis".
Vaccine. 17 (4): 301–7. doi:10.1016/s0264-410x(98)00207-2 (https://doi.org/10.101
6%2Fs0264-410x%2898%2900207-2). PMID 9987167 (https://pubmed.ncbi.nlm.ni
h.gov/9987167).
13. Pasteur L (1881). "Address on the Germ Theory". Lancet. 118 (3024): 271–72.
doi:10.1016/s0140-6736(02)35739-8 (https://doi.org/10.1016%2Fs0140-6736%280
2%2935739-8).
14. "Measles | Vaccination | CDC" (https://www.cdc.gov/measles/vaccination.html).
2018-02-05.
15. Orenstein WA, Bernier RH, Dondero TJ, Hinman AR, Marks JS, Bart KJ, Sirotkin B
(1985). "Field evaluation of vaccine efficacy" (https://www.ncbi.nlm.nih.gov/pmc/art
icles/PMC2536484). Bulletin of the World Health Organization. 63 (6): 1055–68.
16. Jan 11, Hub staff report / Published; 2017 (2017-01-11). "The science is clear:
Vaccines are safe, effective, and do not cause autism" (https://hub.jhu.edu/2017/01
/11/vaccines-autism-public-health-expert/). The Hub. Retrieved 2019-04-16.
17. Ellenberg SS, Chen RT (1997). "The complicated task of monitoring vaccine safety"
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1381831). Public Health Reports.
112 (1): 10–20, discussion 21. PMC 1381831 (https://www.ncbi.nlm.nih.gov/pmc/art
icles/PMC1381831). PMID 9018282 (https://pubmed.ncbi.nlm.nih.gov/9018282).
18. "Vaccine Safety: The Facts" (http://www.healthychildren.org/English/safety-preventi
on/immunizations/Pages/Vaccine-Safety-The-Facts.aspx). HealthyChildren.org.
Retrieved 2019-04-16.
19. Grammatikos AP, Mantadakis E, Falagas ME (June 2009). "Meta-analyses on
pediatric infections and vaccines". Infectious Disease Clinics of North America. 23
(2): 431–57. doi:10.1016/j.idc.2009.01.008 (https://doi.org/10.1016%2Fj.idc.2009.0
1.008). PMID 19393917 (https://pubmed.ncbi.nlm.nih.gov/19393917).
18 of 31 13/03/2021, 13:32
20. Wiedermann, Ursula; Garner-Spitzer, Erika; Wagner, Angelika (January 2016).

"Primary vaccine failure to routine vaccines: Why and what to do?" (https://www.nc
bi.nlm.nih.gov/pmc/articles/PMC4962729). Human Vaccines & Immunotherapeutics.
12 (1): 239–243. doi:10.1080/21645515.2015.1093263 (https://doi.org/10.1080%2
F21645515.2015.1093263). PMC 4962729 (https://www.ncbi.nlm.nih.gov/pmc/articl
es/PMC4962729). PMID 26836329 (https://pubmed.ncbi.nlm.nih.gov/26836329).
21. Neighmond P (2010-02-07). "Adapting Vaccines For Our Aging Immune Systems" (h
ttps://www.npr.org/templates/story/story.php?storyId=123406640). Morning
Edition. NPR. Archived (https://web.archive.org/web/20131216191614/http://www.n
pr.org/templates/story/story.php?storyId=123406640) from the original on
2013-12-16. Retrieved 2014-01-09.
22. Schlegel M, Osterwalder JJ, Galeazzi RL, Vernazza PL (August 1999). "Comparative
efficacy of three mumps vaccines during disease outbreak in Eastern Switzerland:
cohort study" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32261). BMJ. 319
(7206): 352. doi:10.1136/bmj.319.7206.352 (https://doi.org/10.1136%2Fbmj.319.7
206.352). PMC 32261 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32261).
23. Préziosi MP, Halloran ME (September 2003). "Effects of pertussis vaccination on
disease: vaccine efficacy in reducing clinical severity" (https://doi.org/10.1086%2F3
77270). Clinical Infectious Diseases. 37 (6): 772–9. doi:10.1086/377270 (https://do
i.org/10.1086%2F377270). PMID 12955637 (https://pubmed.ncbi.nlm.nih.gov/1295
5637).
24. Miller, E.; Beverley, P. C. L.; Salisbury, D. M. (2002-07-01). "Vaccine programmes
and policies" (https://doi.org/10.1093%2Fbmb%2F62.1.201). British Medical
Bulletin. 62 (1): 201–211. doi:10.1093/bmb/62.1.201 (https://doi.org/10.1093%2Fb
mb%2F62.1.201). ISSN 0007-1420 (https://www.worldcat.org/issn/0007-1420).
25. Orenstein WA, Papania MJ, Wharton ME (May 2004). "Measles elimination in the
United States" (https://doi.org/10.1086%2F377693). The Journal of Infectious
Diseases. 189 Suppl 1 (Suppl 1): S1-3. doi:10.1086/377693 (https://doi.org/10.108
6%2F377693). PMID 15106120 (https://pubmed.ncbi.nlm.nih.gov/15106120).
26. "Measles – United States, January 1 – April 25, 2008" (https://www.cdc.gov/mmwr/p
review/mmwrhtml/mm5718a5.htm). MMWR. Morbidity and Mortality Weekly
Report. 57 (18): 494–8. May 2008. PMID 18463608 (https://pubmed.ncbi.nlm.nih.go
v/18463608). Archived (https://web.archive.org/web/20171011235122/https://www.
cdc.gov/mmwr/preview/mmwrhtml/mm5718a5.htm) from the original on October
11, 2017.
27. "WHO | Smallpox" (https://www.who.int/csr/disease/smallpox/en/). WHO. World
Health Organization. Retrieved 2019-04-16.
28. "WHO South-East Asia Region certified polio-free" (http://www.searo.who.int/mediac
entre/releases/2014/pr1569/en/). WHO. 27 March 2014. Archived (https://web.archi
ve.org/web/20140327235218/http://www.searo.who.int/mediacentre/releases/2014/
pr1569/en/) from the original on 27 March 2014. Retrieved November 3, 2014.
29. "19 July 2017 Vaccines promoted as key to stamping out drug-resistant microbes
"Immunization can stop resistant infections before they get started, say scientists
from industry and academia." " (https://web.archive.org/web/20170722121157/htt
p://www.nature.com/articles/d41586-017-01711-6). Archived from the original (http
s://www.nature.com/articles/d41586-017-01711-6) on July 22, 2017.
19 of 31 13/03/2021, 13:32
30. Sullivan P (2005-04-13). "Maurice R. Hilleman dies; created vaccines" (https://www.

washingtonpost.com/wp-dyn/articles/A48244-2005Apr12.html). Wash. Post.
Archived (https://web.archive.org/web/20121020102622/http://www.washingtonpos
t.com/wp-dyn/articles/A48244-2005Apr12.html) from the original on 2012-10-20.
31. Dudley, Matthew Z; Halsey, Neal A; Omer, Saad B; Orenstein, Walter A; O'Leary,
Sean T; Limaye, Rupali J; Salmon, Daniel A (May 2020). "The state of vaccine safety
science: systematic reviews of the evidence" (https://doi.org/10.1016/S1473-3099
(20)30130-4). The Lancet Infectious Diseases. 20 (5): e80–e89.
doi:10.1016/s1473-3099(20)30130-4 (https://doi.org/10.1016%2Fs1473-3099%282
0%2930130-4). ISSN 1473-3099 (https://www.worldcat.org/issn/1473-3099).
32. Maglione MA, Das L, Raaen L, Smith A, Chari R, Newberry S, Shanman R, Perry T,
Goetz MB, Gidengil C (August 2014). "Safety of vaccines used for routine
immunization of U.S. children: a systematic review" (http://www.escholarship.org/u
c/item/2f93s53t). Pediatrics. 134 (2): 325–37. doi:10.1542/peds.2014-1079 (http
s://doi.org/10.1542%2Fpeds.2014-1079). PMID 25086160 (https://pubmed.ncbi.nl
m.nih.gov/25086160).
33. "Possible Side-effects from Vaccines" (https://www.cdc.gov/vaccines/vac-gen/side-e
ffects.htm). Centers for Disease Control and Prevention. 2018-07-12. Archived (http
s://web.archive.org/web/20170317050028/https://www.cdc.gov/vaccines/vac-gen/si
de-effects.htm) from the original on 17 March 2017. Retrieved 24 February 2014.
34. "Seasonal Flu Shot – Seasonal Influenza (Flu)" (https://web.archive.org/web/201510
01040007/http://www.cdc.gov/flu/about/qa/flushot.htm). CDC. 2018-10-02.
Archived from the original (https://www.cdc.gov/flu/about/qa/flushot.htm) on
2015-10-01. Retrieved 2017-09-17.
35. Wiedermann U, Garner-Spitzer E, Wagner A (2016). "Primary vaccine failure to
routine vaccines: Why and what to do?" (https://www.ncbi.nlm.nih.gov/pmc/articles/
PMC4962729). Human Vaccines and Immunotherapeutics. 12 (1): 239–43.
doi:10.1080/21645515.2015.1093263 (https://doi.org/10.1080%2F21645515.2015.
1093263). ISSN 2164-554X (https://www.worldcat.org/issn/2164-554X).
36. Looker C, Heath K (2011). "No-fault compensation following adverse events
attributed to vaccination: a review of international programmes" (https://www.who.i
nt/bulletin/volumes/89/5/10-081901/en/). Bulletin of the World Health Organization.
Word Health Organisation. 89 (5): 371–8. doi:10.2471/BLT.10.081901 (https://doi.or
g/10.2471%2FBLT.10.081901). PMC 3089384 (https://www.ncbi.nlm.nih.gov/pmc/ar
ticles/PMC3089384). PMID 21556305 (https://pubmed.ncbi.nlm.nih.gov/21556305).
37. "Vaccine Types" (https://www.niaid.nih.gov/topics/vaccines/Pages/typesVaccines.as
px). National Institute of Allergy and Infectious Diseases. 2012-04-03. Archived (htt
ps://web.archive.org/web/20150905205720/http://www.niaid.nih.gov/topics/vaccine
s/Pages/typesVaccines.aspx) from the original on 2015-09-05. Retrieved
2015-01-27.
38. "Types of Vaccines" (https://www.vaccines.gov/basics/types/index.html). Archived
(https://web.archive.org/web/20170729161636/https://www.vaccines.gov/basics/ty
pes/index.html) from the original on 2017-07-29. Retrieved October 19, 2017.
39. "Different Types of Vaccines | History of Vaccines" (https://www.historyofvaccines.or
g/content/articles/different-types-vaccines). www.historyofvaccines.org. Retrieved
2019-06-14.
20 of 31 13/03/2021, 13:32
40. Sinha JK, Bhattacharya S. A Text Book of Immunology (https://books.google.com/bo

oks?id=ytCNCbCWx8oC&pg=PA318) (Google Book Preview). Academic Publishers.
p. 318. ISBN 978-81-89781-09-5. Retrieved 2014-01-09.
41. "Different Types of Vaccines | History of Vaccines" (https://www.historyofvaccines.or
g/content/articles/different-types-vaccines). www.historyofvaccines.org. Retrieved
2019-05-03.
42. "Types of Vaccines" (http://coastalcarolinaresearch.com/types-of-vaccines/).
coastalcarolinaresearch.com. Retrieved 2019-05-03.
43. Philadelphia, The Children's Hospital of (2014-08-18). "A Look at Each Vaccine:
Hepatitis B Vaccine" (https://www.chop.edu/centers-programs/vaccine-education-ce
nter/vaccine-details/vaccine-hepatitis-b-vaccine). www.chop.edu. Retrieved
2019-06-14.
44. "HPV Vaccine | Human Papillomavirus | CDC" (https://www.cdc.gov/vaccines/vpd/hp
v/hcp/vaccines.html). www.cdc.gov. 2019-05-13. Retrieved 2019-06-14.
45. Williamson, E. D.; Eley, S. M.; Griffin, K. F.; Green, M.; Russell, P.; Leary, S. E.;
Oyston, P. C.; Easterbrook, T.; Reddin, K. M. (December 1995). "A new improved
sub-unit vaccine for plague: the basis of protection" (https://doi.org/10.1111%2Fj.1
574-695X.1995.tb00196.x). FEMS Immunology and Medical Microbiology. 12 (3–4):
223–230. doi:10.1111/j.1574-695X.1995.tb00196.x (https://doi.org/10.1111%2Fj.15
74-695X.1995.tb00196.x). ISSN 0928-8244 (https://www.worldcat.org/issn/0928-82
46. "Polysaccharide Protein Conjugate Vaccines" (http://www.globalhealthprimer.emory.
edu/targets-technologies/polysaccharide-protein-conjugate-vaccines.html).
www.globalhealthprimer.emory.edu. Retrieved 2019-06-14.
47. Scott (April 2004). "Classifying Vaccines" (http://www.bioprocessintl.com/multimedi
a/archive/00077/0204su03_77445a.pdf) (PDF). BioProcesses International: 14–23.
Archived (https://web.archive.org/web/20131212222400/http://www.bioprocessintl.
com/multimedia/archive/00077/0204su03_77445a.pdf) (PDF) from the original on
2013-12-12. Retrieved 2014-01-09.
48. Garde, Damian; Feuerstein, Adam (1 November 2020). "How nanotechnology helps
mRNA Covid-19 vaccines work" (https://www.statnews.com/2020/12/01/how-nanote
chnology-helps-mrna-covid19-vaccines-work/). STAT. Retrieved 21 December 2020.
49. CDC (11 February 2020). "COVID-19 and Your Health" (https://www.cdc.gov/coronav
irus/2019-ncov/vaccines/different-vaccines/mrna.html). Centers for Disease Control
and Prevention. Retrieved 21 December 2020.
50. Banks, Marcus A. (16 July 2020). "What Are mRNA Vaccines, and Could They Work
Against COVID-19?" (https://www.smithsonianmag.com/science-nature/mrna-vaccin
es-covid-19-180975330/). Smithsonian Magazine. Retrieved 21 December 2020.
51. Branswell, Helen (19 December 2020). "FDA grants authorization to Moderna's
Covid-19 vaccine" (https://www.statnews.com/2020/12/18/fda-eua-moderna-vaccin
e-covid19/). STAT. Retrieved 21 December 2020.
52. Kim W, Liau LM (January 2010). "Dendritic cell vaccines for brain tumors" (https://w
ww.ncbi.nlm.nih.gov/pmc/articles/PMC2810429). Neurosurgery Clinics of North
America. 21 (1): 139–57. doi:10.1016/j.nec.2009.09.005 (https://doi.org/10.1016%
2Fj.nec.2009.09.005). PMC 2810429 (https://www.ncbi.nlm.nih.gov/pmc/articles/PM
C2810429). PMID 19944973 (https://pubmed.ncbi.nlm.nih.gov/19944973).
53. Anguille S, Smits EL, Lion E, van Tendeloo VF, Berneman ZN (June 2014). "Clinical
use of dendritic cells for cancer therapy". The Lancet. Oncology. 15 (7): e257-67.
doi:10.1016/S1470-2045(13)70585-0 (https://doi.org/10.1016%2FS1470-2045%281
3%2970585-0). PMID 24872109 (https://pubmed.ncbi.nlm.nih.gov/24872109).
21 of 31 13/03/2021, 13:32
54. McKenzie, David (26 May 2018). "Fear and failure: How Ebola sparked a global
health revolution" (https://edition.cnn.com/2018/05/26/health/ebola-outbreaks-west
-africa-congo-revolution-mckenzie-intl/index.html). CNN. Retrieved 26 May 2018.
55. Meri S, Jördens M, Jarva H (December 2008). "Microbial complement inhibitors as
vaccines". Vaccine. 26 Suppl 8: I113-7. doi:10.1016/j.vaccine.2008.11.058 (https://
doi.org/10.1016%2Fj.vaccine.2008.11.058). PMID 19388175 (https://pubmed.ncbi.n
lm.nih.gov/19388175).
56. Lowe (2008). "Plasmid DNA as Prophylactic and Therapeutic vaccines for Cancer
and Infectious Diseases" (http://www.horizonpress.com/pla). Plasmids: Current
Research and Future Trends. Caister Academic Press. ISBN 978-1-904455-35-6.
57. "Monovalent (https://web.archive.org/web/20090628224336/http://www.mercksour
ce.com/pp/us/cns/cns_hl_dorlands_split.jsp?pg=/ppdocs/us/common/dorlands/dorla
nd/five/000067458.htm.htm)" at Dorland's Medical Dictionary
58. Polyvalent vaccine (http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQz
pgzEzzSzppdocszSzuszSzcommonzSzdorlandszSzdorlandzSz000113928zPzhtm) at
Dorlands Medical Dictionary Archived (https://web.archive.org/web/201203071301
21/http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocsz
SzuszSzcommonzSzdorlandszSzdorlandzSz000113928zPzhtm) March 7, 2012, at
the Wayback Machine
59. "Questions And Answers On Monovalent Oral Polio Vaccine Type 1 (mOPV1)'Issued
Jointly By WHO and UNICEF' " (https://web.archive.org/web/20120229143829/http://
www.pediatriconcall.com/fordoctor/medical_original_articles/oral_polio_vaccine.asp)
. Pediatric Oncall. 2 (8). 3. What advantages does mOPV1 have over trivalent oral
polio vaccine (tOPV)?. 2005-01-08. Archived from the original (http://www.pediatric
oncall.com/fordoctor/Medical_original_articles/oral_polio_vaccine.asp) on
2012-02-29.
60. Sutter RW, Cochi SL, Melnick JL (1999). "Live attenuated polio vaccines". In Plotkin
SA, Orenstein WA (eds.). Vaccines. Philadelphia: W. B. Saunders. pp. 364–408.
61. Kanesa-thasan N, Sun W, Kim-Ahn G, Van Albert S, Putnak JR, King A,
Raengsakulsrach B, Christ-Schmidt H, Gilson K, Zahradnik JM, Vaughn DW, Innis BL,
Saluzzo JF, Hoke CH (April 2001). "Safety and immunogenicity of attenuated
dengue virus vaccines (Aventis Pasteur) in human volunteers". Vaccine. 19
(23–24): 3179–88. CiteSeerX 10.1.1.559.8311 (https://citeseerx.ist.psu.edu/viewdo
c/summary?doi=10.1.1.559.8311). doi:10.1016/S0264-410X(01)00020-2 (https://do
i.org/10.1016%2FS0264-410X%2801%2900020-2). PMID 11312014 (https://pubme
d.ncbi.nlm.nih.gov/11312014).
62. Engler, Renata J. M.; Greenwood, John T.; Pittman, Phillip R.; Grabenstein, John D.
(2006-08-01). "Immunization to Protect the US Armed Forces: Heritage, Current
Practice, and Prospects" (https://doi.org/10.1093%2Fepirev%2Fmxj003).
Epidemiologic Reviews. 28 (1): 3–26. doi:10.1093/epirev/mxj003 (https://doi.org/1
0.1093%2Fepirev%2Fmxj003). ISSN 0193-936X (https://www.worldcat.org/issn/019
3-936X). PMID 16763072 (https://pubmed.ncbi.nlm.nih.gov/16763072).
63. Sox, Harold C.; Liverman, Catharyn T.; Fulco, Carolyn E.; War, Institute of Medicine
(US) Committee on Health Effects Associated with Exposures During the Gulf
(2000). Vaccines (https://www.ncbi.nlm.nih.gov/books/NBK222854/). National
Academies Press (US).
64. "Institute for Vaccine Safety – Thimerosal Table" (http://www.vaccinesafety.edu/thi-t
able.htm). Archived (https://web.archive.org/web/20051210210622/http://www.vac
cinesafety.edu/thi-table.htm) from the original on 2005-12-10.
22 of 31 13/03/2021, 13:32
65. Wharton, Melinda E.; National Vaccine Advisory committee "U.S.A. national vaccine
plan" (https://www.hhs.gov/nvpo/vacc_plan/) Archived (https://web.archive.org/web
/20160504053302/http://www.hhs.gov/nvpo/vacc_plan) 2016-05-04 at the Wayback
Machine
66. "Measurements of Non-gaseous air pollutants > Metals" (https://web.archive.org/w
eb/20070929124159/http://www.npl.co.uk/environment/vam/nongaseouspollutants/
ngp_metals.html). npl.co.uk. National Physics Laboratory. Archived from the
original (http://www.npl.co.uk/environment/vam/nongaseouspollutants/ngp_metals.
html) on 29 September 2007. Retrieved 28 June 2020.
67. "Thimerosal in vaccines" (https://www.fda.gov/BiologicsBloodVaccines/SafetyAvaila
bility/VaccineSafety/UCM096228). Center for Biologics Evaluation and Research,
U.S. Food and Drug Administration. 2007-09-06. Archived (https://web.archive.org/
web/20130106215029/https://www.fda.gov/BiologicsBloodVaccines/SafetyAvailabilit
y/VaccineSafety/UCM096228) from the original on 2013-01-06. Retrieved
2007-10-01.
68. Bigham M, Copes R (2005). "Thiomersal in vaccines: balancing the risk of adverse
effects with the risk of vaccine-preventable disease". Drug Safety. 28 (2): 89–101.
doi:10.2165/00002018-200528020-00001 (https://doi.org/10.2165%2F00002018-2
00528020-00001). PMID 15691220 (https://pubmed.ncbi.nlm.nih.gov/15691220).
S2CID 11570020 (https://api.semanticscholar.org/CorpusID:11570020).
69. Offit PA (September 2007). "Thimerosal and vaccines – a cautionary tale" (https://s
emanticscholar.org/paper/c2f25efef0ed507beef6bce8f4bf33cb6f51e524). The New
England Journal of Medicine. 357 (13): 1278–9. doi:10.1056/NEJMp078187 (https://
doi.org/10.1056%2FNEJMp078187). PMID 17898096 (https://pubmed.ncbi.nlm.nih.g
ov/17898096). S2CID 36318722 (https://api.semanticscholar.org/CorpusID:3631872
2).
70. March 5, Reuters Updated; 2019 (2019-03-05). "Another study, this one of 657k
kids, finds MMR vaccine doesn't cause autism | Montreal Gazette" (https://nationalp
ost.com/news/world/the-largest-ever-study-has-shown-the-measles-mumps-and-rub
ella-vaccine-is-linked-to-lower-rates-of-autism). Retrieved 2019-03-13.
71. Hoffman J (2019-03-05). "One More Time, With Big Data: Measles Vaccine Doesn't
Cause Autism" (https://www.nytimes.com/2019/03/05/health/measles-vaccine-autis
m.html). The New York Times. ISSN 0362-4331 (https://www.worldcat.org/issn/0362
-4331). Retrieved 2019-03-13.
72. CDC (2018-07-12). "Ingredients of Vaccines – Fact Sheet" (https://www.cdc.gov/vac
cines/vac-gen/additives.htm). Archived (https://web.archive.org/web/20091217193
639/http://www.cdc.gov/vaccines/vac-gen/additives.htm) from the original on
December 17, 2009. Retrieved December 20, 2009.
73. The mercury levels in the table, unless otherwise indicated, are taken from:
Mercury Levels in Commercial Fish and Shellfish (1990-2010) (https://www.fda.gov/
Food/FoodborneIllnessContaminants/Metals/ucm115644.htm) Archived (https://we
b.archive.org/web/20150503155319/https://www.fda.gov/Food/FoodborneIllnessCon
taminants/metals/ucm115644.htm) 2015-05-03 at the Wayback Machine U.S. Food
and Drug Administration. Accessed 8 January 2012.
74. Centers for Disease Control and Prevention, U.S. Vaccine Names (https://www.cdc.g
ov/vaccines/about/terms/USVaccines.html), archived (https://web.archive.org/web/2
0160526212322/http://www.cdc.gov/vaccines/about/terms/USVaccines.html) from
the original on 2016-05-26, retrieved 2016-05-21.
75. Centers for Disease Control and Prevention (2018-08-07), Tetanus (Lockjaw)
Vaccination (https://www.cdc.gov/vaccines/vpd-vac/tetanus/), archived (https://we
b.archive.org/web/20160516034254/http://www.cdc.gov/vaccines/vpd-vac/tetanus/)
from the original on 2016-05-16, retrieved 2016-05-21.
23 of 31 13/03/2021, 13:32
76. Centers for Disease Control and Prevention (2018-02-02), Vaccine Acronyms and
Abbreviations [Abbreviations used on U.S. immunization records] (https://www.cdc.
gov/vaccines/terms/vacc-abbrev.html), archived (https://web.archive.org/web/2017
0602192710/https://www.cdc.gov/vaccines/terms/vacc-abbrev.html) from the
original on 2017-06-02, retrieved 2017-05-22.
77. "Principles and considerations for adding a vaccine to a national immunization
programme" (https://apps.who.int/iris/bitstream/handle/10665/111548/978924150
6892_eng.pdf) (PDF). World Health Organization. 1 April 2014. Archived (https://we
b.archive.org/web/20200929164919/https://apps.who.int/iris/bitstream/handle/106
65/111548/9789241506892_eng.pdf) (PDF) from the original on 29 September
2020. Retrieved 17 August 2020.
78. Wijnans, Leonoor; Voordouw, Bettie (11 December 2015). "A review of the changes
to the licensing of influenza vaccines in Europe" (https://www.ncbi.nlm.nih.gov/pmc
/articles/PMC4687503). Influenza and Other Respiratory Viruses. 10 (1): 2–8.
doi:10.1111/irv.12351 (https://doi.org/10.1111%2Firv.12351). ISSN 1750-2640 (http
s://www.worldcat.org/issn/1750-2640). PMC 4687503 (https://www.ncbi.nlm.nih.gov
/pmc/articles/PMC4687503). PMID 26439108 (https://pubmed.ncbi.nlm.nih.gov/264
39108).
79. Offit, Paul A. (2020). "Making vaccines: Licensure, recommendations and
requirements" (https://www.chop.edu/centers-programs/vaccine-education-center/
making-vaccines/licensure-recommendations-and-requirements). Children's
Hospital of Philadelphia. Archived (https://web.archive.org/web/20200908060918/h
ttps://www.chop.edu/centers-programs/vaccine-education-center/making-vaccines/l
icensure-recommendations-and-requirements) from the original on 8 September
2020. Retrieved 20 August 2020.
80. Toner E, Barnill A, Krubiner C, Bernstein J, Privor-Dumm L, Watson M, et al. (2020).
Interim Framework for COVID-19 Vaccine Allocation and Distribution in the United
States (https://www.centerforhealthsecurity.org/our-work/pubs_archive/pubs-pdfs/2
020/200819-vaccine-allocation.pdf) (PDF) (Report). Baltimore, MD: Johns Hopkins
Center for Health Security. Archived (https://web.archive.org/web/20200822093641
/https://www.centerforhealthsecurity.org/our-work/pubs_archive/pubs-pdfs/2020/20
0819-vaccine-allocation.pdf) (PDF) from the original on 22 August 2020. Retrieved
24 August 2020.
81. Dooling K, Marin M, Wallace M, McClung N, Chamberland M, Lee GM, et al.
(December 2020). "The Advisory Committee on Immunization Practices' Updated
Interim Recommendation for Allocation of COVID-19 Vaccine – United States,
December 2020" (https://doi.org/10.15585%2Fmmwr.mm695152e2). MMWR.
Morbidity and Mortality Weekly Report. 69 (5152): 1657–1660.
doi:10.15585/mmwr.mm695152e2 (https://doi.org/10.15585%2Fmmwr.mm695152
e2). PMID 33382671 (https://pubmed.ncbi.nlm.nih.gov/33382671).
82. "Vaccine product approval process" (https://web.archive.org/web/20200927144627/
https://www.fda.gov/vaccines-blood-biologics/development-approval-process-cber/v
accine-product-approval-process). U.S. Food and Drug Administration (FDA). 30
January 2020. Archived from the original (https://www.fda.gov/vaccines-blood-biolo
gics/development-approval-process-cber/vaccine-product-approval-process) on 27
September 2020. Retrieved 17 August 2020.
83. "ACIP Vaccine Recommendations Home Page" (https://www.cdc.gov/vaccines/hcp/a
cip-recs/index.html). CDC. 2013-11-15. Archived (https://web.archive.org/web/2013
1231054216/http://www.cdc.gov/vaccines/hcp/acip-recs/index.html) from the
original on 2013-12-31. Retrieved 2014-01-10.
24 of 31 13/03/2021, 13:32
84. "Vaccine Status Table" (http://aapredbook.aappublications.org/site/news/vaccstatu

s.xhtml). Red Book Online. American Academy of Pediatrics. April 26, 2011.
Archived (https://web.archive.org/web/20131227223436/http://aapredbook.aappubl
ications.org/site/news/vaccstatus.xhtml) from the original on December 27, 2013.
Retrieved January 9, 2013.
85. "HPV Vaccine Safety" (https://www.cdc.gov/vaccinesafety/Vaccines/HPV/Index.html)
. Centers for Disease Control and Prevention (CDC). 2013-12-20. Archived (https://
web.archive.org/web/20091110193757/http://www.cdc.gov/vaccinesafety/Vaccines/
HPV/Index.html) from the original on 2009-11-10. Retrieved 2014-01-10.
86. "HPV vaccine in the clear" (http://www.nhs.uk/news/2009/09September/Pages/Cervi
cal-cancer-vaccine-QA.aspx). NHS choices. 2009-10-02. Archived (https://web.archi
ve.org/web/20140110093039/http://www.nhs.uk/news/2009/09September/Pages/C
ervical-cancer-vaccine-QA.aspx) from the original on 2014-01-10. Retrieved
2014-01-10.
87. Goodman JL (2005-05-04). "Statement by Jesse L. Goodman, M.D., M.P.H. Director
Center for Biologics, Evaluation and Research Food and Drug Administration U.S.
Department of Health and Human Services on US Influenza Vaccine Supply and
Preparations for the Upcoming Influenza Season before Subcommittee on Oversight
and Investigations Committee on Energy and Commerce United States House of
Representatives" (https://www.hhs.gov/asl/testify/t050504b.html). Archived (http
s://web.archive.org/web/20080921163050/http://www.hhs.gov/asl/testify/t050504b.
html) from the original on 2008-09-21. Retrieved 2008-06-15.
88. Olesen OF, Lonnroth A, Mulligan B (January 2009). "Human vaccine research in the
European Union" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115654).
Vaccine. 27 (5): 640–5. doi:10.1016/j.vaccine.2008.11.064 (https://doi.org/10.101
6%2Fj.vaccine.2008.11.064). PMC 7115654 (https://www.ncbi.nlm.nih.gov/pmc/arti
cles/PMC7115654). PMID 19059446 (https://pubmed.ncbi.nlm.nih.gov/19059446).
89. Jit M, Newall AT, Beutels P (April 2013). "Key issues for estimating the impact and
cost-effectiveness of seasonal influenza vaccination strategies" (https://www.ncbi.n
lm.nih.gov/pmc/articles/PMC3903903). Human Vaccines & Immunotherapeutics. 9
(4): 834–40. doi:10.4161/hv.23637 (https://doi.org/10.4161%2Fhv.23637).
90. Newall AT, Reyes JF, Wood JG, McIntyre P, Menzies R, Beutels P (February 2014).
"Economic evaluations of implemented vaccination programmes: key
methodological challenges in retrospective analyses". Vaccine. 32 (7): 759–65.
91. Roser, Max; Vanderslott, Samantha (2013-05-10). "Vaccination" (https://ourworldin
data.org/vaccination). Our World in Data.
92. Hardman Reis T (2006). "The role of intellectual property in the global challenge for
immunization". J World Intellect Prop. 9 (4): 413–25.
doi:10.1111/j.1422-2213.2006.00284.x (https://doi.org/10.1111%2Fj.1422-2213.20
06.00284.x).
93. "www.who.int" (https://www.who.int/phi/publications/Increasing_Access_to_Vaccines
_Through_Technology_Transfer.pdf) (PDF). Archived (https://web.archive.org/web/20
151123091841/http://www.who.int/phi/publications/Increasing_Access_to_Vaccines_
Through_Technology_Transfer.pdf) (PDF) from the original on 2015-11-23.
25 of 31 13/03/2021, 13:32
94. "Three ways to make a vaccine" (https://www.washingtonpost.com/wp-dyn/content/

graphic/2009/11/24/GR2009112401834.html?sid=ST2009112401941)
(infographic). Archived (https://web.archive.org/web/20151223231412/http://www.
washingtonpost.com/wp-dyn/content/graphic/2009/11/24/GR2009112401834.html?
sid=ST2009112401941) from the original on 2015-12-23. Retrieved 2015-08-05, in
Stein, Rob (24 November 2009). "Vaccine system remains antiquated" (https://ww
w.washingtonpost.com/wp-dyn/content/story/2009/11/24/ST2009112401941.html?s
id=ST2009112401941). The Washington Post. Archived (https://web.archive.org/we
b/20171019084922/http://www.washingtonpost.com/wp-dyn/content/story/2009/11
/24/ST2009112401941.html?sid=ST2009112401941) from the original on 19
October 2017.
95. Muzumdar JM, Cline RR (2009). "Vaccine supply, demand, and policy: a primer" (htt
ps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185851). Journal of the American
Pharmacists Association. 49 (4): e87-99. doi:10.1331/JAPhA.2009.09007 (https://do
i.org/10.1331%2FJAPhA.2009.09007). PMC 7185851 (https://www.ncbi.nlm.nih.gov/
pmc/articles/PMC7185851). PMID 19589753 (https://pubmed.ncbi.nlm.nih.gov/1958
9753).
96. "Components of a vaccine" (http://vaccine-safety-training.org/vaccine-components.
html). Archived (https://web.archive.org/web/20170613192256/http://vaccine-safet
y-training.org/vaccine-components.html) from the original on 2017-06-13.
97. Bae K, Choi J, Jang Y, Ahn S, Hur B (April 2009). "Innovative vaccine production
technologies: the evolution and value of vaccine production technologies". Archives
of Pharmacal Research. 32 (4): 465–80. doi:10.1007/s12272-009-1400-1 (https://do
i.org/10.1007%2Fs12272-009-1400-1). PMID 19407962 (https://pubmed.ncbi.nlm.ni
h.gov/19407962). S2CID 9066150 (https://api.semanticscholar.org/CorpusID:90661
50).
98. "Vaccine Taskforce Aims" (https://assets.publishing.service.gov.uk/government/uplo
ads/system/uploads/attachment_data/file/893417/S0135_Vaccine_Taskforce_Aims.p
df) (PDF). assets.publishing.service.gov.uk. 6 April 2020. Retrieved 2020-07-26.
99. Pagliusi, Sonia; Jarrett, Stephen; Hayman, Benoit; Kreysa, Ulrike; Prasad, Sai D.;
Reers, Martin; Hong Thai, Pham; Wu, Ke; Zhang, Youn Tao; Baek, Yeong Ok; Kumar,
Anand (July 2020). "Emerging manufacturers engagements in the COVID −19
vaccine research, development and supply" (https://www.ncbi.nlm.nih.gov/pmc/arti
cles/PMC7287474). Vaccine. 38 (34): 5418–5423.
22). PMC 7287474 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287474).
100. Miller, Joe; Kuchler, Hannah (2020-04-28). "Drugmakers race to scale up vaccine
capacity" (https://www.ft.com/content/87d1170a-78bc-11ea-bd25-7fd923850377).
www.ft.com. Retrieved 2020-07-26.
101. Plotkin, Stanley A.; Orenstein, Walter A.; Offit, Paul A. (2012). Vaccines. Elsevier
Health Sciences. p. 40. ISBN 9781455700905.
102. Plotkin, Stanley A.; Orenstein, Walter A.; Offit, Paul A. (2012). Vaccines. Elsevier
Health Sciences. p. 41. ISBN 9781455700905.
103. Morein B, Hu KF, Abusugra I (June 2004). "Current status and potential application
of ISCOMs in veterinary medicine". Advanced Drug Delivery Reviews. 56 (10):
1367–82. doi:10.1016/j.addr.2004.02.004 (https://doi.org/10.1016%2Fj.addr.2004.0
2.004). PMID 15191787 (https://pubmed.ncbi.nlm.nih.gov/15191787).
104. American Medicine (https://books.google.com/books?id=yvxXAAAAMAAJ).
American-Medicine Publishing Company. 1926.
26 of 31 13/03/2021, 13:32
105. South African Institute for Medical Research (1929). Annual report [Jaarverslag] (htt
ps://books.google.com/books?id=KzAXAAAAIAAJ). South African Institute for
Medical Research – Suid-Afrikaanse Instituut vir Mediese Navorsing.
106. Khan FA (2011-09-20). Biotechnology Fundamentals (https://books.google.com/boo
ks?id=-s5oRDUuMSIC&pg=PA270). CRC Press. p. 270. ISBN 978-1-4398-2009-4.
107. Giudice EL, Campbell JD (April 2006). "Needle-free vaccine delivery". Advanced
Drug Delivery Reviews. 58 (1): 68–89. doi:10.1016/j.addr.2005.12.003 (https://doi.o
rg/10.1016%2Fj.addr.2005.12.003). PMID 16564111 (https://pubmed.ncbi.nlm.nih.g
ov/16564111).
108. WHO to trial Nanopatch needle-free delivery system| ABC News, 16 Sep 2014|
"Needle-free polio vaccine a 'game-changer' " (http://www.abc.net.au/news/2014-0
9-16/vaxxas-says-needle-free-polio-vaccine-a-game-changer/5748072).
2014-09-16. Archived (https://web.archive.org/web/20150402210010/http://www.a
bc.net.au/news/2014-09-16/vaxxas-says-needle-free-polio-vaccine-a-game-changer
/5748072) from the original on 2015-04-02. Retrieved 2015-09-15.
109. "Australian scientists develop 'needle-free' vaccination" (http://www.smh.com.au/te
chnology/sci-tech/needleless-trial-set-for-start-20130417-2i0qw.html). The Sydney
Morning Herald. 18 August 2013. Archived (https://web.archive.org/web/201509250
12246/http://www.smh.com.au/technology/sci-tech/needleless-trial-set-for-start-201
30417-2i0qw.html) from the original on 25 September 2015.
110. "Vaxxas raises $25m to take Brisbane's Nanopatch global" (https://web.archive.org/
web/20150316002836/http://www.brw.com.au/p/tech-gadgets/brisbane_nanopatch
_the_reverse_brain_DPyEGHC1ih6919r8X37SdO). Business Review Weekly.
2015-02-10. Archived from the original (http://www.brw.com.au/p/tech-gadgets/bris
bane_nanopatch_the_reverse_brain_DPyEGHC1ih6919r8X37SdO) on 2015-03-16.
111. "Australian scientists develop 'needle-free' vaccination" (http://www.thehindu.com/
sci-tech/health/medicine-and-research/australian-scientists-develop-needlefree-vac
cination/article2493365.ece). The Hindu. Chennai, India. 28 September 2011.
Archived (https://web.archive.org/web/20140101162738/http://www.thehindu.com/
sci-tech/health/medicine-and-research/australian-scientists-develop-needlefree-vac
cination/article2493365.ece) from the original on 1 January 2014.
112. "Needle-free nanopatch vaccine delivery system" (http://www.news-medical.net/ne
ws/20110803/Needle-free-nanopatch-vaccine-delivery-system.aspx). News Medical.
3 August 2011. Archived (https://web.archive.org/web/20120511203129/http://ww
w.news-medical.net/news/20110803/Needle-free-nanopatch-vaccine-delivery-syste
m.aspx) from the original on 11 May 2012.
113. Patel JR, Heldens JG (March 2009). "Immunoprophylaxis against important virus
disease of horses, farm animals and birds" (https://www.ncbi.nlm.nih.gov/pmc/articl
es/PMC7130586). Vaccine. 27 (12): 1797–1810. doi:10.1016/j.vaccine.2008.12.063
(https://doi.org/10.1016%2Fj.vaccine.2008.12.063). PMC 7130586 (https://www.ncb
i.nlm.nih.gov/pmc/articles/PMC7130586). PMID 19402200 (https://pubmed.ncbi.nl
m.nih.gov/19402200).
114. Berkelman RL (August 2003). "Human illness associated with use of veterinary
vaccines" (https://doi.org/10.1086%2F375595). Clinical Infectious Diseases. 37 (3):
407–14. doi:10.1086/375595 (https://doi.org/10.1086%2F375595). PMID 12884166
(https://pubmed.ncbi.nlm.nih.gov/12884166).
27 of 31 13/03/2021, 13:32
115. van Oirschot JT, Rziha HJ, Moonen PJ, Pol JM, van Zaane D (June 1986).
"Differentiation of serum antibodies from pigs vaccinated or infected with
Aujeszky's disease virus by a competitive enzyme immunoassay" (https://doi.org/1
0.1099%2F0022-1317-67-6-1179). The Journal of General Virology. 67 ( Pt 6) (6):
1179–82. doi:10.1099/0022-1317-67-6-1179 (https://doi.org/10.1099%2F0022-131
7-67-6-1179). PMID 3011974 (https://pubmed.ncbi.nlm.nih.gov/3011974).
116. van Oirschot JT (August 1999). "Diva vaccines that reduce virus transmission".
Journal of Biotechnology. 73 (2–3): 195–205. doi:10.1016/S0168-1656(99)00121-2
(https://doi.org/10.1016%2FS0168-1656%2899%2900121-2). PMID 10486928 (http
s://pubmed.ncbi.nlm.nih.gov/10486928).
117. van Oirschot JT, Gielkens AL, Moormann RJ, Berns AJ (June 1990). "Marker vaccines,
virus protein-specific antibody assays and the control of Aujeszky's disease".
Veterinary Microbiology. 23 (1–4): 85–101. doi:10.1016/0378-1135(90)90139-M (ht
tps://doi.org/10.1016%2F0378-1135%2890%2990139-M). PMID 2169682 (https://p
ubmed.ncbi.nlm.nih.gov/2169682).
118. Kaashoek MJ, Moerman A, Madić J, Rijsewijk FA, Quak J, Gielkens AL, van Oirschot JT
(April 1994). "A conventionally attenuated glycoprotein E-negative strain of bovine
herpesvirus type 1 is an efficacious and safe vaccine". Vaccine. 12 (5): 439–44.
doi:10.1016/0264-410X(94)90122-8 (https://doi.org/10.1016%2F0264-410X%289
119. Hulst MM, Westra DF, Wensvoort G, Moormann RJ (September 1993). "Glycoprotein
E1 of hog cholera virus expressed in insect cells protects swine from hog cholera"
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC237945). Journal of Virology. 67
(9): 5435–42. doi:10.1128/JVI.67.9.5435-5442.1993 (https://doi.org/10.1128%2FJVI.
67.9.5435-5442.1993). PMC 237945 (https://www.ncbi.nlm.nih.gov/pmc/articles/PM
C237945). PMID 8350404 (https://pubmed.ncbi.nlm.nih.gov/8350404).
120. Capua I, Terregino C, Cattoli G, Mutinelli F, Rodriguez JF (February 2003).
"Development of a DIVA (Differentiating Infected from Vaccinated Animals) strategy
using a vaccine containing a heterologous neuraminidase for the control of avian
influenza". Avian Pathology. 32 (1): 47–55. doi:10.1080/0307945021000070714 (ht
tps://doi.org/10.1080%2F0307945021000070714). PMID 12745380 (https://pubme
d.ncbi.nlm.nih.gov/12745380). S2CID 22827454 (https://api.semanticscholar.org/Co
rpusID:22827454).
121. Maas A, Meens J, Baltes N, Hennig-Pauka I, Gerlach GF (November 2006).
"Development of a DIVA subunit vaccine against Actinobacillus pleuropneumoniae
infection". Vaccine. 24 (49–50): 7226–37. doi:10.1016/j.vaccine.2006.06.047 (http
s://doi.org/10.1016%2Fj.vaccine.2006.06.047). PMID 17027123 (https://pubmed.nc
bi.nlm.nih.gov/17027123).
122. Leyman B, Boyen F, Van Parys A, Verbrugghe E, Haesebrouck F, Pasmans F (May
2011). "Salmonella Typhimurium LPS mutations for use in vaccines allowing
differentiation of infected and vaccinated pigs" (https://biblio.ugent.be/publication/
1201519). Vaccine. 29 (20): 3679–85. doi:10.1016/j.vaccine.2011.03.004 (https://d
oi.org/10.1016%2Fj.vaccine.2011.03.004). hdl:1854/LU-1201519 (https://hdl.handl
e.net/1854%2FLU-1201519). PMID 21419163 (https://pubmed.ncbi.nlm.nih.gov/214
19163). Archived (https://web.archive.org/web/20171028043359/https://biblio.ugen
t.be/publication/1201519) from the original on 2017-10-28.
123. Needham, Joseph (2000). Science and Civilisation in China: Volume 6, Biology and
Biological Technology, Part 6, Medicine. Cambridge University Press. p. 154.
ISBN 9780521632621.
124. Williams G (2010). Angel of Death. Basingstoke: Palgrave Macmillan.
ISBN 978-0-230-27471-6.
28 of 31 13/03/2021, 13:32
125. Silverstein, Arthur M. (2009). A History of Immunology (2nd ed.). Academic Press.

p. 293. ISBN 9780080919461.
126. Fenner, F.; Henderson, D.A.; Arita, I.; Jezek, Z.; Ladnyi, I.D. (1988). Smallpox and its
Eradication. Geneva: World Health Organization. ISBN 92-4-156110-6.
127. Baxby, Derrick (1984). "A Death from Inoculated Smallpox in the English Royal
Family" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1139449). Med Hist. 28 (3):
303–07. doi:10.1017/s0025727300035961 (https://doi.org/10.1017%2Fs002572730
128. Stern AM, Markel H (2005). "The history of vaccines and immunization: familiar
patterns, unew challenges" (https://doi.org/10.1377%2Fhlthaff.24.3.611). Health
Affairs. 24 (3): 611–621. doi:10.1377/hlthaff.24.3.611 (https://doi.org/10.1377%2Fh
lthaff.24.3.611). PMID 15886151 (https://pubmed.ncbi.nlm.nih.gov/15886151).
129. Dunn PM (January 1996). "Dr Edward Jenner (1749-1823) of Berkeley, and
vaccination against smallpox" (https://web.archive.org/web/20110708080506/htt
p://fn.bmjjournals.com/content/74/1/F77.full.pdf) (PDF). Archives of Disease in
Childhood: Fetal and Neonatal Edition. 74 (1): F77-8. doi:10.1136/fn.74.1.F77 (http
s://doi.org/10.1136%2Ffn.74.1.F77). PMC 2528332 (https://www.ncbi.nlm.nih.gov/p
mc/articles/PMC2528332). PMID 8653442 (https://pubmed.ncbi.nlm.nih.gov/865344
2). Archived from the original (http://fn.bmjjournals.com/content/74/1/F77.full.pdf)
(PDF) on 2011-07-08.
130. Baxby, Derrick (1984). "A Death from Inoculated Smallpox in the English Royal
Family" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1139449). Med Hist. 28 (3):
303–07. doi:10.1017/s0025727300035961 (https://doi.org/10.1017%2Fs002572730
131. Van Sant JE (2008). "The Vaccinators: Smallpox, Medical Knowledge, and the
'Opening' of Japan". J Hist Med Allied Sci. 63 (2): 276–79. doi:10.1093/jhmas/jrn014
(https://doi.org/10.1093%2Fjhmas%2Fjrn014).
132. Didgeon JA (May 1963). "Development of Smallpox Vaccine in England in the
Eighteenth and Nineteenth Centuries" (https://www.ncbi.nlm.nih.gov/pmc/articles/P
MC2124036). British Medical Journal. 1 (5342): 1367–72.
doi:10.1136/bmj.1.5342.1367 (https://doi.org/10.1136%2Fbmj.1.5342.1367).
133. Louten, Jennifer (2016). Essential Human Virology. Academic Press. pp. 134–135.
ISBN 9780128011713.
134. Baarda BI, Sikora AE (2015). "Proteomics of Neisseria gonorrhoeae: the treasure
hunt for countermeasures against an old disease" (https://www.ncbi.nlm.nih.gov/p
mc/articles/PMC4620152). Frontiers in Microbiology. 6: 1190.
doi:10.3389/fmicb.2015.01190 (https://doi.org/10.3389%2Ffmicb.2015.01190).
PMID 26579097 (https://pubmed.ncbi.nlm.nih.gov/26579097); Access provided by
the University of Pittsburgh.
135. Alarcon JB, Waine GW, McManus DP (1999). "DNA Vaccines: Technology and
Application as Anti-parasite and Anti-microbial Agents". Advances in Parasitology
Volume 42. Advances in Parasitology. 42. pp. 343–410.
doi:10.1016/S0065-308X(08)60152-9 (https://doi.org/10.1016%2FS0065-308X%28
08%2960152-9). ISBN 9780120317424. PMID 10050276 (https://pubmed.ncbi.nlm.
nih.gov/10050276).
29 of 31 13/03/2021, 13:32
136. Robinson HL, Pertmer TM (2000). DNA vaccines for viral infections: basic studies
and applications. Advances in Virus Research. 55. pp. 1–74.
doi:10.1016/S0065-3527(00)55001-5 (https://doi.org/10.1016%2FS0065-3527%280
0%2955001-5). ISBN 9780120398553. PMID 11050940 (https://pubmed.ncbi.nlm.ni
h.gov/11050940).
137. Naftalis, Kramer Levin; Royzman, Frankel LLP-Irena; Pineda, ré. "Third-Generation
Vaccines Take Center Stage in Battle Against COVID-19 | Lexology" (https://www.lex
ology.com/library/detail.aspx?g=04bdfa93-c8ea-4654-a5f1-c659fc4769c8).
www.lexology.com. Retrieved 24 January 2021.
138. Regalado, Antonio. "The U.S. government has begun testing its first Zika vaccine in
humans" (https://www.technologyreview.com/s/602073/us-government-starts-test-
of-zika-vaccine-in-humans/?set=602081). Retrieved 2016-08-06.
139. Chen Y, Wang S, Lu S (February 2014). "DNA Immunization for HIV Vaccine
Development" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494200). Vaccines.
2 (1): 138–59. doi:10.3390/vaccines2010138 (https://doi.org/10.3390%2Fvaccines2
140. Staff (28 March 2013). "Safer vaccine created without virus" (http://www.japantime
s.co.jp/news/2013/03/28/world/safer-vaccine-created-without-virus/#.VcLHxGCPKM
_). The Japan Times. Agence France-Presse – Jiji Press. Archived (https://web.archiv
e.org/web/20130330142043/http://www.japantimes.co.jp/news/2013/03/28/world/s
afer-vaccine-created-without-virus/#.VcLHxGCPKM_) from the original on 30 March
2013. Retrieved 2013-03-28.
141. Spohn G, Bachmann MF (February 2008). "Exploiting viral properties for the
rational design of modern vaccines". Expert Review of Vaccines. 7 (1): 43–54.
doi:10.1586/14760584.7.1.43 (https://doi.org/10.1586%2F14760584.7.1.43).
PMID 18251693 (https://pubmed.ncbi.nlm.nih.gov/18251693). S2CID 40130001 (htt
ps://api.semanticscholar.org/CorpusID:40130001).
142. Samuelsson O, Herlitz H (March 2008). "Vaccination against high blood pressure: a
new strategy". Lancet. 371 (9615): 788–9. doi:10.1016/S0140-6736(08)60355-4 (h
ttps://doi.org/10.1016%2FS0140-6736%2808%2960355-4). PMID 18328909 (http
s://pubmed.ncbi.nlm.nih.gov/18328909). S2CID 38323966 (https://api.semanticsch
olar.org/CorpusID:38323966).
143. Poland GA, Jacobson RM, Ovsyannikova IG (May 2009). "Trends affecting the future
of vaccine development and delivery: the role of demographics, regulatory science,
the anti-vaccine movement, and vaccinomics" (https://www.ncbi.nlm.nih.gov/pmc/a
rticles/PMC2693340). Vaccine. 27 (25–26): 3240–4.
144. Sala F, Manuela Rigano M, Barbante A, Basso B, Walmsley AM, Castiglione S
(January 2003). "Vaccine antigen production in transgenic plants: strategies, gene
constructs and perspectives". Vaccine. 21 (7–8): 803–8.
doi:10.1016/s0264-410x(02)00603-5 (https://doi.org/10.1016%2Fs0264-410x%280
145. Kumar GB, Ganapathi TR, Revathi CJ, Srinivas L, Bapat VA (October 2005).
"Expression of hepatitis B surface antigen in transgenic banana plants". Planta.
222 (3): 484–93. doi:10.1007/s00425-005-1556-y (https://doi.org/10.1007%2Fs004
25-005-1556-y). PMID 15918027 (https://pubmed.ncbi.nlm.nih.gov/15918027).
S2CID 23987319 (https://api.semanticscholar.org/CorpusID:23987319).
30 of 31 13/03/2021, 13:32
146. Ostachuk AI, Chiavenna SM, Gómez C, Pecora A, Pérez-Filgueira MD, Escribano JM,
Ardila F, Dus MJ, Santos AW (2009). "Expression of a ScFv–E2T fusion protein in
CHO-K1 cells and alfalfa transgenic plants for the selective directioning to antigen
presenting cells" (https://www.academia.edu/355962). Veterinary Immunology and
Immunopathology. 128 (1): 315. doi:10.1016/j.vetimm.2008.10.224 (https://doi.org
/10.1016%2Fj.vetimm.2008.10.224). Archived (https://web.archive.org/web/201805
01013416/http://www.academia.edu/355962/Ostachuk_AI_-_Expression_of_a_ScFv-
E2T_fusion_protein_in_CHO-K1_cells_and_alfalfa_transgenic_plants_for_the_selectiv
e_directioning_to_antigen_presenting_cells) from the original on 2018-05-01.
147. Peréz Aguirreburualde MS, Gómez MC, Ostachuk A, Wolman F, Albanesi G, Pecora
A, Odeon A, Ardila F, Escribano JM, Dus Santos MJ, Wigdorovitz A (February 2013).
"Efficacy of a BVDV subunit vaccine produced in alfalfa transgenic plants".
Veterinary Immunology and Immunopathology. 151 (3–4): 315–24.
doi:10.1016/j.vetimm.2012.12.004 (https://doi.org/10.1016%2Fj.vetimm.2012.12.0
External links
Vaccines and Antisera (https://curlie.org/Health/Ph External video
armacy/Drugs_and_Medications/Vaccines_and_Anti Modern Vaccine and
sera) at Curlie Adjuvant Production and
WHO Vaccine preventable diseases and Characterization (https://www.y
immunization (http://www.emro.who.int/entity/vpi/) outube.com/watch?v=mq-PgsVY
World Health Organization position papers on -VU), Genetic Engineering &
vaccines (https://www.who.int/immunization/docu Biotechnology News
ments/positionpapers/en/)
The History of Vaccines (http://www.historyofvacci
nes.org/), from the College of Physicians of Philadelphia
This website was highlighted by Genetic Engineering & Biotechnology News in
its "Best of the Web" section in January 2015. See: "The History of Vaccines". Best
of the Web. Genetic Engineering & Biotechnology News. 35 (2). 15 January 2015. p. 38.
University of Oxford Vaccinology Programme: a series of short courses in
vaccinology (https://web.archive.org/web/20160411114041/https://www.conted.ox.
ac.uk/courses/professional/staticdetails.php?course=227)
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Even if the host does develop antibodies, protection might not be

Adjuvants commonly are used to boost immune response,

e eﬃcacy or performance of the vaccine is dependent on a

the disease itself (for some diseases vaccination

e following are important considerations in the eﬀectiveness of a vaccination program:[24]

e measles vaccine is estimated to prevent a million deaths every year.[30]

Host-("vaccinee")-related determinants that render a person susceptible to infection, such as genetics,

ere are several types of vaccines in use.[37] ese represent

Some vaccines contain inactivated, but previously virulent, micro-

cultivated under conditions that disable their virulent

Avian ﬂu vaccine development by reverse

Toxoid vaccines are made from inactivated toxic

vaccine made from Mycobacterium bovis to protect against tuberculosis.[47]

A number of innovative vaccines are also in development and in

Dendritic cell vaccines combine dendritic cells with

World Health Organization

e process requires manufacturing consistency at WHO-contracted laboratories following Good

Aer the antigen is generated, it is isolated from the cells used to

e development of new delivery systems raises the hope of

Notable developments in vaccine delivery technologies have

An experimental needle-free[108] vaccine delivery system is undergoing animal testing.[109][110] A stamp-

Where rabies occurs, rabies vaccination of dogs may be required by

Mary Wortley Montagu, who had witnessed variolation in Turkey,

standard method of virus propagation for vaccines.[133]

e twentieth century saw the introduction of several successful

First generation vaccines are whole-organism vaccines – either live

Second generation vaccines were developed to reduce the risks

Plants as bioreactors for vaccine production

20. Wiedermann, Ursula; Garner-Spitzer, Erika; Wagner, Angelika (January 2016).

30. Sullivan P (2005-04-13). "Maurice R. Hilleman dies; created vaccines" (https://www.

40. Sinha JK, Bhattacharya S. A Text Book of Immunology (https://books.google.com/bo

84. "Vaccine Status Table" (http://aapredbook.aappublications.org/site/news/vaccstatu

94. "Three ways to make a vaccine" (https://www.washingtonpost.com/wp-dyn/content/

125. Silverstein, Arthur M. (2009). A History of Immunology (2nd ed.). Academic Press.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Vaccine&oldid=1011708171"

This page was last edited on 12 March 2021, at 11:15 (UTC).

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