Infect Chemother.

2020 Jun;52(2):e28
https://doi.org/10.3947/ic.2020.52.e28
pISSN 2093-2340·eISSN 2092-6448

Review Article Empirical Treatment and Prevention of

COVID-19

Hyoung-Shik Shin

Infectious Diseases Specialist, Korean Society of Zoonoses, Seoul, Korea

Received: May 22, 2020

ABSTRACT
Corresponding Author:
Hyoung-Shik Shin, MD, PhD The rapid spread of severe acute respiratory coronavirus syndrome 2 (SARS-CoV-2) in the
Infectious Diseases Specialist, Korean Society population and throughout the cells within our body has been developing. Another major
of Zoonoses, 806, Seocho Town Trapalace, 23 cycle of coronavirus disease 2019 (COVID-19), which is expected in the coming fall, could
Seocho-daero 74 gil, Seocho-gu, Seoul 06621, be even more severe than the current one. Therefore, effective countermeasures should be
Korea.
developed based on the already obtained clinical and research information about SARS-
Tel: +82-10-8651-7617
E-mail: [email protected] CoV-2. The aim of this review was to summarize the data on the empirical treatment of
COVID-19 acquired during this SARS-CoV-2 infection cycle; this would aid the establishment
Copyright © 2020 by The Korean Society of an appropriate healthcare policy to meet the challenges in the future. The infectious
of Infectious Diseases, Korean Society for
disease caused by SARS-CoV-2 is characterized by common cold along with hypersensitivity
Antimicrobial Therapy, and The Korean Society
for AIDS reaction. Thus, in addition to treating common cold, it is essential to minimize the
This is an Open Access article distributed exposure of cells to the virus and to mitigate the uncontrolled immune response. A
under the terms of the Creative Commons proper combination of antiviral agents, immune modulators such as prednisolone, and
Attribution Non-Commercial License (https:// anticoagulants such as heparin and anti-C5a antagonists could be employed to minimize
creativecommons.org/licenses/by-nc/4.0/)
lung damage and prevent systemic involvements. Finally, strategies to achieve population
which permits unrestricted non-commercial
use, distribution, and reproduction in any
immunity against SARS-CoV-2 should be developed through understanding of the interaction
medium, provided the original work is properly between the immune system and the virus.
cited.
Keywords: COVID-19; SARS-CoV-2; Coronavirus; Treatment; Prevention
ORCID iDs
Hyoung-Shik Shin
https://orcid.org/0000-0001-6504-3413
INTRODUCTION
Conflict of Interest
No conflicts of interest.
Novel coronavirus (severe acute respiratory coronavirus syndrome 2, SARS-CoV-2) has been
Author Contributions rapidly spreading in the population [1] as well as throughout the cells within their bodies
Conceptualization: HSS. Writing - original [2, 3]. To date, it has been around 4 months that the whole world suffered from it. Another
draft: HSS. Writing - review & editing: HSS. major cycle of the infection is expected in the coming fall from the northern hemisphere
which would be even more severe than the first one [4]. Therefore, it is important to develop
more effective countermeasures based on the scientific data obtained during the first round
of coronavirus disease 2019 (COVID-19).

Our previous article defined the nature of the infectious diseases as the hypersensitivity
reaction by the virus and presented the basic treatments based on the hypersensitivity
pneumonitis (HP) [5, 6]. The diagnosis of COVID-19 can be empirically achieved by one or

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Empirical Treatment and Prevention of COVID-19

more of the following: 1) clinical symptoms, 2) radiologic imaging studies such as chest
computed tomography or magnetic resonance imaging of central nervous system, and 3)
detection of virus by real-time reverse transcriptase polymerase chain reaction/serology.

The aim of this review is to present empirical treatment and preventive strategies for
COVID-19 based on the accumulated experience in managing the disease, which may aid in
clarifying the confusion associated with research results and would help shape the healthcare
policies. However, researchers should consider the fact that the data published currently in
scientific journals might be somewhat biased because of the turbulent environment due to
the COVID-19 pandemic. Therefore, the proposed guidelines should be revised as soon as
new and reliable research data are available.

MEDICATIONS FOR COMMON COLD

Though the COVID-19 showed pandemic spread and unexpected clinical manifestations
characterized by various symptoms throughout the whole body, SARS-CoV-2 seems to be
less virulent especially in children and adolescents, in whom the disease mimics common
cold caused by seasonal coronaviruses [7]. Therefore, basic therapeutic approaches used
for common cold would be effective in case of mild symptoms and further treatment is not
required in the absence of any other clinical manifestations [8]. Table 1 summarizes the
treatments used for common cold including that caused by coronaviruses.

Non-steroidal anti-inflammatory drugs (NSAIDs) can be safely used for 2 - 3 days without
affecting the pentose phosphate pathway. In contrast, acetaminophen can increase reactive
oxygen species in the cell and induce cell death [9, 10]. However, use of NSAIDs can result
in hypersensitivity [11] and acute thromboembolic events [12]. There were a few reports
regarding concerns that NSAIDs can weaken the immune system if applied a week or longer
[10, 13]. Prednisolone is safer and more efficacious, considering that it can overcome the
overall inflammatory process in a cell by suppressing the diverse kind of cytokines including
interleukins and tumor necrosis factor-α [14]. Hydrocortisone is considered the best
medicine with fewer side effects.

Pseudoephedrine at dose of 10 - 20 mg is effective for the protection of epithelial cells by

raising the intracellular cyclic guanosine monophosphate [15]. Antihistamine can help lessen
the vascular permeability by blocking the platelet activating factor [16] and alleviate allergic
symptoms [17]. Cimetidine can improve the heartburn symptom and elevate the immune

Table 1. Medications for common cold

Class/Symptoms Drug
Analgesics for pain and fever Prednisolone 10 mg PO
Hydrocortisone 25 - 50 mg PO
Ibuprofen, naproxen, and other NSAIDs: be cautious to hypersensitivity reactions and acute thromboembolic
side effects.
Aspirin can cause Reye's syndrome
Antihistamines for runny nose Diphenhydramine, loratadine, fexofenadine, cetirizine, levocetirizine, etc.
Decongestants for stuffy nose Pseudoephedrine: contraindicated for the patients with uncontrolled high blood pressure
Anti-tussives Dextromethorphan, codeine.
Phosphodiesterase inhibitor, nonselective Theophylline at low doses (100 - 200 mg PO twice per day)
Immune modulators with antibacterial effect Azithromycin, clarithromycin
PO, per os.

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Empirical Treatment and Prevention of COVID-19

functions [18]. Theophylline at low doses (100 – 200 mg twice daily), the medicine applied
to the treatment of asthma for a long time, can be administered safely. It can protect alveolar
epithelium with the suppression of cytokine-inducible nitric oxide synthase (NOS) and
raising intracellular cyclic adenosine monophosphate [19]. Macrolide antibiotics including
azithromycin cause few side effects and their early application can support epithelial cells
for some time [20]. Macrolides transform gut microbiome so that they protect against the
respiratory virus and strengthen endothelial NOS pathway [20-22].

Human immunodeficiency virus (HIV) non-nucleoside reverse transcriptase inhibitors

(NNRTIs) such as rilpivirine described below can be used for the patients with common
cold symptoms preemptively, instead of all medications mentioned above. That is what we
experienced the effect of oseltamivir in the 2009 Influenza (H1N1) pandemic.

TREATMENT FOR PNEUMONIA

At the early stage of the epidemic, it had been recommended to apply the treatment regimen
of middle east respiratory syndrome coronavirus (MERS-CoV) in the case of the patients
with severe symptoms [23]. An interim guideline was suggested by the members of Korean
Society of Infectious Diseases (KSID) in April, 2020 [24]. This treatment strategy is further
proposed with taking into consideration of the KSID guideline. Pneumonia features observed
in COVID-19 are similar to that of HP. Therefore, it is needed to follow the application of basic
treatment strategy for HP [14], which is to prevent cell exposure to the virus and to abate
the excessive immune reactions. In addition to this treatment strategy, it is needed to apply
anticoagulants [25, 26]. It is required not to interrupt the initiation of adaptive immunity
as augmenting the innate immune system. Another purpose of the treatment regimen in
this review is to sustain lifeforce without the application of the mechanical ventilator and
extracorporeal membrane oxygenation and thereby to result in the blockade of breakdown of
healthcare system (Table 2).

The aim of the administration of antiviral agents is to lessen the exposure to antigen (virus).
Ribonucleic acid (RNA) dependent RNA polymerization is considered as a crucial step in the
RNA virus because SARS-CoV-2 is positive sense single-stranded (ss)RNA virus. Unfortunately,
it appeared to be controversial to apply remdesivir that was developed for the negative sense
ssRNA virus such as Ebola virus [27, 28]. Also, side effects of remdesivir were not well known,
and its intravenous administration can cause another burden to the healthcare system. Safer
medicine is the best for patients as an empirical regimen. Treatment with most nucleotide/
nucleoside inhibitors is theoretically applicable [29, 30]. Tenofovir disoproxil fumarate/
emtricitabine (TDF/FTC), which has been prescribed for HIV-infected or hepatitis B virus-
infected patients for a long time can be used safely as a short-term medicine for COVID-19
patients. Despite the unfavorable result in a small case series study [31], TDF/FTC would serve a
good candidate because of its high concentration in the epithelium and safety profile.

An in vivo study showed that an HIV NNRTI rilpivirine was very effective against positive sense
ssRNA Zika virus [32]. There was a report on HIV NNRTIs to be effective with the molecular
docking by computational simulation [33]. Furthermore, it was reported that rilpivirine had
comparable efficacy to remdesivir in vitro [34]. Antiviral therapy has the best effect when
administered for a minimum of 5 days and a maximum of 14 days to avoid unexpected side
effects; earlier discontinuation should be considered if clinical progress is evident, including

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Empirical Treatment and Prevention of COVID-19

Table 2. Treatments for pneumonia

Anti-viral agents
Drug Duration Remark
Nucleotide/nucleoside analogues Remdesivir, tenofovir/emtricitabine 5 - 14 days Acyclovir, famciclovir, and ganciclovir
need to be studied
HIV NNRTIs Rilpivirine, efavirenz, etravirine 5 - 14 days Doravirine may be efficacious.
HIV protease inhibitors Lopinavir/ritonavir, darunavir/ritonavir or 5 - 14 days
cobicistat, atazanavir
Antimalarials Chloroquine, hydroxychloroquine, 3 days Mefloquine should be administered
mefloquine up to 5 tablets.
Corticosteroids
Severity of pneumonia Treatment Duration Remark
Mild pneumonia Steroid inhaler or prednisolone Preemptive: 5 - 7 days Prednisolone is safer than
10 - 20 mg PO Therapeutic: 5 - 21 days methylprednisolone. Hydrocortisone
Moderate pneumonia Prednisolone 30 mg PO Not recommended after 300 mg/day can be used for patients
3 weeks of illness, except with unexpected side effects.
for cases with proliferative
inflammation on biopsy.
Severe/critical pneumonia Prednisolone 40 mg once or twice daily PO, Rapid tapering is required.
or methylprednisolone 1mg/kg/day IV
Antibiotics for other coinfections/superinfections
Severity of pneumonia, or coinfection Treatment Duration Remark
Mild pneumonia Ceftriaxone or macrolide Around 3 days Macrolide, cephalosporin, and
(azithromycin/clarithromycin) glycopeptide antimicrobial increases
Moderate pneumonia Ceftriaxone + macrolide Around 7 days the innate immunity
± teicoplanin/vancomycin
Severe/critical pneumonia Vancomycin + macrolide 7 - 14 days Consider the epidemiologic patterns
± meropenem of microbes
Influenza Oseltamivir 5 days Consider false negative result of the
rapid diagnostic test
Anticoagulants: Recommended for patients with anyone of followings; 1) patients of ≥65 years 2) dyspnea and hypoxia requiring 3L/min oxygen to correct
hypoxemia, 3) respiratory rate >24/min, 4) decreased consciousness, 5) unstable vital signs, 6) patients requiring mechanical ventilation, hemodialysis, CRRT, or
ECMO. Preemptive use is preferable to decrease lung sequelae, if available.
Drug Administration route/dose
Heparin IV, SQ, inhalation; heparin has a thrombolytic effect.
IV unfractionated heparin sulfate; initial dose: 80 units/kg bolus (maximum = 10,000 units), initial infusion rate: 18
units/kg/h (maximum = 23,000 units/h), then adjust the target aPTT range (60 - 85)
Nebulized unfractionated heparin sulfate 10,000 - 25,000U every 4h (height ≥165 cm) or every 6 hours (height <165 cm)
Anti-C5a antagonist IV; inhalation/nebulization may be possible.
Camostat mesylate/nafamostat mesylate IV; the efficacy could be limited due to suppression of C3b and C5b facilitation.
Warfarin PO; preemptive and prophylactic use is considered for high-risk patients. Drug interactions are common.
Interferon: 1) Interferon-β 1b, mainly by Inhalation. Consider the combination of SQ + inhalation. 2) Patients of the age ≥70 years are indicated. Consider the
administration of interferon for the high-risk patients of ≥40 years. The maximum effect of interferon will be achieved within 3 days of the onset of COVID-19. 3)
Duration: 7 days for patients of ≥70 years, 14 days for the patients of ≥80 years and high-risk patients
Antipyretics: Hydrocortisone 25 – 50 mg PO/IV, or prednisolone 10 mg PO
Phosphodiesterase type-5 inhibitors (sildenafil): rescue therapy (50 mg PO every 8 h) for patients with impending respiratory failure
Epinephrine: nebulization/endotracheal/IV; emergency use for patients showing acute hypersensitivity reactions with shock
HIV, human immunodeficiency virus; NNRTI, non-nucleoside reverse transcriptase inhibitor; PO, per os; IV, intravenously; CRRT, continuous renal replacement
therapy; ECMO, extracorporeal membrane oxygenation; SQ, subcutaneously; aPTT, activated partial thromboplastin time.
All medications should be administered with caution as they might cause unexpected hypersensitivity reactions and serious side effects. Older medications
are desirable but may have minor side effects that are easy to control. All medications can be used preemptively for patients with symptoms of pneumonia or
systemic involvement and can be adjusted based on the ideal body weight, but should be prescribed for children at recommended doses.

clearance of symptoms, improved immune response, resolution of pneumonia as revealed by

chest radiography. However, patients aged 65 years and older [35] or those with the impaired
immune status due to diabetes mellitus, hypertension, and other conditions could receive the
drugs beforehand and for a longer time.

Lopinavir/ritonavir does not appear to be a promising treatment for COVID-19 [36], although
it was reported to have good efficacy for the treatment of SARS [37]. It may be effective
to apply the kind of antimalarial drugs such as chloroquine, hydroxychloroquine, and

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Empirical Treatment and Prevention of COVID-19

mefloquine [10, 29, 38], however, side effects are concerned due to higher doses than those
generally used for the treatment of malaria. It may be better not to exceed the treatment
doses and period for malaria. The mechanism of azithromycin seems to be efficacious by
strengthening the innate immunity [20] rather than antiviral efficacy against SARS-CoV-2
[38]. Serine protease inhibitors [39] such as camostat mesylate/nafamostat mesylate are
limited options as they suppress the facilitation of C3b and C5b [40].

Antiviral agents should be prescribed at the earlier stage of pneumonia to stop the
progression to acute respiratory distress syndrome. If the supply of medicine is not enough,
it can also be started around 5 - 7 days after the infection. Even so, antiviral treatment should
be given to the patients with older age or risk factors such as diabetes mellitus, hypertension,
or immunosuppressive disorders immediately.

As for the COVID-19, the application of steroids can be the basis for the treatment since the
main symptom might be developed due to hypersensitivity reaction [14]. Although the various
steroid inhaler could be effective, oral administration of prednisolone up to 0.5 mg/kg per day
can treat a moderate degree of pneumonia. The nebulization with hydrocortisone would be safer
among steroid inhalers. Prednisolone 40 mg per 12 hours PO is recommended to the patients
with severe pneumonia [41]. In the case of patients requiring intensive care, the equivalent
dose of methylprednisolone/hydrocortisone can be administered intravenously [42]. The short
term treatment for 5 - 7 days for moderate pneumonia may be preferable [41]. The duration of
administration for the severe cases can be extended to 10 - 21 days after the onset of infection
until the immune function is optimal. If the clinical improvement of COVID-19 becomes obvious,
rapid tapering is needed for optimal immune function. Although hyperinflammation by elevated
cytokines such as IL-1, IL-6, or TNF-α can contribute to the lung damage, certain anti-cytokine
strategy would be not good enough to suppress the whole inflammatory process [43].

In the case of severe/critical pneumonia, anticoagulants have to be applied as a basic

treatment regimen [40] to help avoiding the use of mechanical ventilation or extracorporeal
membrane oxygenation. It is required to make an adequate choice according to the symptom
of the patients among warfarin, heparin [44], or camostat mesylate/nafamostat mesylate.
Warfarin can be administered to high-risk groups from the beginning of infection as an
oral medication. Because anti-C5a antagonist is not easily accessible and very expensive,
inhalation of heparin [45] is more suitable in the case of lung involvement. Furthermore,
injection of heparin is required for thrombin lysis if a patient shows symptoms of
thromboembolism. Rapid alleviation of symptoms can be expected with intravenous
administration of heparin and an anti-C5a antagonist in combination, especially in cases
when the virus invades the central nervous system; therefore, camostat mesylate/nafamostat
mesylate are not recommended as they suppress the formation of C3b and C5b [40].

Interferon (INF)β-1b is the most effective among various INFs [23] and is recommended in
combination with other antiviral agents. INF treatment should initiate within three days
of infection [23] and the duration of the treatment should depend on the age and immune
status. A one- and two-week treatment regimen is recommended for people in their 70s and
80s, respectively, and longer treatment is recommended for those with weakened innate
immunity [35].

Antibiotics can be used empirically for the treatment of superimposed/combined bacterial

pneumonia. Vancomycin [46], teicoplanin [46, 47], and azithromycin [20, 38], which are

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Empirical Treatment and Prevention of COVID-19

expected to show efficacy against SARS-CoV-2, can be administered. If secondary infections

emerge in intensive care units, the epidemiology profile of multidrug-resistant bacteria at
the hospital should be taken into account, and an empirical combination of vancomycin/
teicoplanin, meropenem, and macrolides can be used. Country-specific influenza trends should
also be considered, and if a rapid diagnostic test is positive, oseltamivir is the treatment of
choice; it should also be employed if false negative results are obtained for patients with typical
flu symptoms, patients who are elderly (65 years and older), or those on immunosuppressants.

Phosphodiesterase type-5 inhibitors may relieve acute exudative damage in the lungs via
the downregulation of proinflammatory and profibrotic cytokines induced in response to
reactive oxygen species, thereby representing a rescue therapeutic modality [48]. Epinephrine
should be also used in patients with acute hypersensitivity reactions with shock.

It should be always kept in mind that overtreatment may trigger and/or worsen efferocytosis
or cause side effects; therefore, the clinical status of the patients should be closely monitored
and even small changes should be considered for treatment adjustments.

PREVENTION OF RAPID SPREAD AND DISEASE

PROGRESSION OF SARS-CoV-2
At present, it is not likely that effective strategies to block the spread of SARS-CoV-2 have
already been developed in the present crisis and we can expect nothing more than the
initiation of appropriate immune responses to lower the exposure to the virus. Changes in
virus characteristics during the HIV epidemic provide a glimpse of how SARS-CoV-2 could
evolve depending on the immune response. We can assume that the faster transmissibility
(and/or higher pathogenicity) appears as the virus circulates in the elderly who have weaker
innate immunity, while the slower transmissibility (and/or lower pathogenicity) appears in
the younger people who have higher innate immunity. It can also be expected that individuals
with allergic disorders may show a different clinical course and/or more severe symptoms
than the general population.

To prevent infection and initiate appropriate immunity to the virus, a sufficient level of
air circulation indoors, cough etiquette and maintenance of hand hygiene are required.
Furthermore, social and physical distancing among people should help prevent the
breakdown of the medical system. It also seems reasonable to allow a temporary increase
in patient numbers to the level which can be managed by the current medical system. These
strategies also include appropriate healthcare policies, for example acquisition of herd
immunity, which has been adopted in Sweden [49]. With proper measures, it is quite possible
that we should be able to overcome the expected second wave predicted in the northern
hemisphere in the coming late fall and winter [4].

It is quite unlikely that adaptive immunity would be activated with a vaccine that induces
IgG via antibody-dependent immune enhancement, similar to the one observed in case of
infection with the Dengue virus [50]. It should also be noted that convalescent serum therapy
may be harmful. Therefore, increasing of nonspecific innate immunity is needed surely for
the elderly and the people with defective innate immunity. Increasing innate immunity in the
epithelium as the first line defense is as follows. Moderate mountain hiking can lead to the
increase of muscle tissue and strengthen the lung capacity [51]. Being exposed to nature will

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Empirical Treatment and Prevention of COVID-19

lead to an increase of innate immunity by the sound microbiome [52]. In addition, spending
time on the beach such as, playing, reading, or swimming would be effective in reducing the
viral load infected to upper respiratory tracts [53].

It is well known that probiotics such as Lactobacillus spp. can enhance immunity. Vitamin D
supplements also reinforce the resilience against the virus as it enhances immunity [54].
Antibiotics of macrolides kinds, metronidazole, trimethoprim/sulfamethoxazole, dapsone may
help increase the immunity as well [55]. Rosiglitazone and pioglitazone can promote innate
immunity as a PPAR-γ agonist [56]. Cimetidine which is helpful in the case of heartburn will
enhance immunity [18]. BCG vaccine can stimulate the immune system [57]. Also, the innate
immunity of T lymphocyte can be elevated by the application of RNA delivery into cells [58].

PERSPECTIVE FOR THE FUTURE RESEARCH

The precise therapeutic mechanisms of the medications recommended in this review should
be clarified in future studies, and the efficacy of antiviral agents and anticoagulants needs
to be confirmed in randomized controlled trials. A bulk of clinical and research data cannot
be interpreted at present. Considering that the infection can be asymptomatic and as it can
rapidly spread across national borders, studies—to elucidate the life cycle of SARS-CoV-2,
innate and adaptive immune responses to the virus, and side effects of medications—
should be conducted on a global scale; this would help in developing appropriate treatment
strategies. Studies pertaining to the lifestyle, including diet, living conditions, and working
environment, and hospital policies are also necessary. Considering the high intracellular
concentration of TDF/FTC in the epithelium, short-term preexposure and postexposure
prophylaxis with TDF/FTC or rilpivirine for healthcare workers and high-risk groups could be
useful [59, 60] and its effectiveness should be evaluated. In addition, the short course of TDF/
FTC can contribute to decrease viral shedding in stool.

Vaccine development is urgent. As it is challenging to produce a proper vaccine that takes

into consideration the interaction between the immune system and coronaviruses such as
SARS-CoV-2, comprehensive studies should be attempted using several viral strains and
up-to-date techniques as well as conventional approaches, including inactivated whole virus.
Furthermore, the efficacy of different inoculation methods should be compared.

There are several reports on the status of SARS-CoV and MERS-CoV survivors, including
their low lung capacity and cognitive problems [61-63]. Systematic studies are required to
address these complications. Isolation restricts motor activity, which would add considerable
physical and mental problems for patients with deteriorated lung function, especially those
in intensive care units. If possible, various rehabilitation activities are recommended at
the beginning of the isolation rather than after recovery. Considering that SARS-CoV-2 is
less virulent in the younger population, employment of young healthcare workers should
contribute to prevention of secondary infections and accelerate patient recovery.

CONCLUSION
SARS-CoV-2 is a virus that causes common cold and various hypersensitivity reactions. The
lack of immunity against SARS-CoV-2 results in the worldwide spread of COVID-19, a novel

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Empirical Treatment and Prevention of COVID-19

disease with diverse clinical manifestations and pathophysiological mechanisms. After the
initial confusion among the scientific community and healthcare professionals, extensive basic
and clinical research has been conducted to understand the course of COVID-19 and reactions
triggered by SARS-CoV-2 in the host. These findings could contribute to our understanding of
the pathophysiology not only of COVID-19 but also of other infectious diseases.

We need to analyze the data obtained through evaluation of COVID-19 survivors as well as
COVID-19-related deaths, so that the losses associated with the pandemic can be minimized.
It is also necessary to evaluate our natural environments and review the extensive scientific
data obtained in the past, so that better solutions for combating the next wave could be
identified. Strategies developed through analysis of the current pandemic should prepare us
for future crises caused by pathogens more lethal than SARS-CoV-2.

ACKNOWLEDGMENTS
I am grateful to Dr. Dong-Gyun Lim (immunologist at National Medical Center, Seoul,
Korea), Dr. Yoon-keun Kim (allergist, immunologist, and CEO at MD Healthcare, Seoul,
Korea), and Dr. Sang Il Kim (President, Committee of Emerging Infectious Diseases of
Korean Society of Infectious Diseases) for sharing their inspiring ideas. I also would like to
thank Jeewon Lee for the translating the present manuscript.

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