This document outlines the topics to be covered in a microbiology course on immunology. It introduces innate immunity, including anatomical barriers like skin and mucous membranes, antimicrobial peptides, the complement system, pattern recognition receptors, and inflammatory mediators. Adaptive immunity is also introduced, distinguishing it from innate immunity by its antigen specificity, immunological memory, and involvement of lymphocytes. Key immune cells involved in innate responses are described.
This document outlines the topics to be covered in a microbiology course on immunology. It introduces innate immunity, including anatomical barriers like skin and mucous membranes, antimicrobial peptides, the complement system, pattern recognition receptors, and inflammatory mediators. Adaptive immunity is also introduced, distinguishing it from innate immunity by its antigen specificity, immunological memory, and involvement of lymphocytes. Key immune cells involved in innate responses are described.
This document outlines the topics to be covered in a microbiology course on immunology. It introduces innate immunity, including anatomical barriers like skin and mucous membranes, antimicrobial peptides, the complement system, pattern recognition receptors, and inflammatory mediators. Adaptive immunity is also introduced, distinguishing it from innate immunity by its antigen specificity, immunological memory, and involvement of lymphocytes. Key immune cells involved in innate responses are described.
This document outlines the topics to be covered in a microbiology course on immunology. It introduces innate immunity, including anatomical barriers like skin and mucous membranes, antimicrobial peptides, the complement system, pattern recognition receptors, and inflammatory mediators. Adaptive immunity is also introduced, distinguishing it from innate immunity by its antigen specificity, immunological memory, and involvement of lymphocytes. Key immune cells involved in innate responses are described.
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Microbiology 532: Immunology
Dennis E. Lopatin, Ph.D.
Dept. of Biologic and Materials Sciences 4209 Dental Building
Office Hours by Appointment
Phone: 647-3912 Electronic mail: [email protected] Helpful Hints Readings in text are beneficial I expect you to read the relevant chapters in Nester. Understanding the concepts is not optional Think, rather than memorize Test questions are based on concepts Ask questions Dont wait until the last minute to study Check the website Lecture 1 Immunology Introduction & Innate immunity Why Does a Dentist Need to Understand Immunology? Many of the oral diseases have an immune component Periodontal disease Caries Sjgrens Syndrome Current and future therapeutics affect the immune system and oral health Systemic and Oral diseases are interrelated Cooperation with other health care professional requires a common language
What is immunity? Protection from infection, tumors, etc. Innate immunity is always available Adaptive immunity distinguishes self from non-self and involves immune system education Responses that may result in host tissue damage Two types of immunity Innate immunity (not antigen-specific) Anatomical barriers Mechanical Biochemical Non-specific (eg. Low pH in stomach) Receptor-driven (eg. PAMP-recognition) Adaptive immunity (antigen-specific) Receptor-driven Pre-existing clones programmed to make a specific immune response (humoral/cellular) Antigen A substance (antigen) that is capable of reacting with the products of a specific immune response, e.g., antibody or specific sensitized T-lymphocytes. A self component may be considered an antigen even though one does not generally make immune responses against those components. Characteristics of Adaptive Immunity Immune response is highly specific for the antigen that triggered it. Receptors on surface of immune cells have same specificity as the antibody/effector activity that will be generated Exposure to antigen creates an immunologic memory. Due to clonal expansion and creation of a large pool of cells committed to that antigen Subsequent exposure to the same antigen results in a rapid and vigorous response Components of the immune system Cells involved in immunity platelets megakaryocyte eosinophil neutrophil basophil mast cell common myeloid progenitor
monocyte macrophage Natural Killer cell
plasma cell B Lymphocyte T Lymphocyte
common lymphoid progenitor
Pluripotent hematopoietic stem cell Blood Serum or Plasma Leukocytes, Platelets and RBC Serum Proteins Mononuclear Cells Polymorphonuclear leukocytes (or Granulocytes) Immunoglobulins Complement Clotting factors Many others Neutrophils Eosinophils Basophils Lymphocytes (T cells, B cells & NK cells) Monocytes Where is that stuff? Lymphoid Organs Primary or central lymphoid organs bone marrow and thymus where lymphocytes are generated Secondary or peripheral lymphoid organs where adaptive immune responses are initiated Distribution of Lymphoid Tissues Response to Initial Infection Stages of Response to Infection Course of Typical Acute Infection Innate Host Defense Mechanisms Anatomic Factors Mechanical Factors Biochemical Factors Skin Stratified and cornified epithelium provides a mechanical barrier Indigenous microbiota competes with pathogens Acid pH inhibits growth of disease producing bacteria Bactericidal long chain fatty acids in sebaceous gland secretions Respiratory Tract Upper Respiratory Tract Nasal hairs induce turbulence Mucous secretions trap particles Mucous stream to the base of tongue where material is swallowed Nasal secretions contain antimicrobial substances Upper respiratory tract contains large resident flora Lower Respiratory Tract Particles trapped on mucous membranes of bronchi and bronchioles Beating action of cilia causes mucociliary stream to flow up into the pharynx where it is swallowed 90% of particles removed this way. Only smallest particles (<10 in diameter) reach alveoli Alveoli Alveolar macrophage rapidly phagocytize small particles Alimentary Tract General defense mechanisms Mucous secretions Integrity of of mucosal epithelium Peristaltic motions of the gut propel contents downward Secretory antibody and phagocytic cells Stomach Generally sterile due to low pH Small Intestine Upper portion contains few bacteria As distal end of ilieum is reached flora increases Colon Enormous numbers of microorganisms 50-60% of fecal dry weight is bacteria Genitourinary Tract Male No bacteria above urethrovesicular junction Frequent flushing action of urine Bactericidal substances from prostatic fluid pH of urine Bladder mucosal cells may be phagocytic Urinary sIgA Female (Vagina) Large microbial population (lactobacilli) Microorganisms produce low pH due to breakdown of glycogen produced by mucosal cells Eye Flushing action of tears which drain through the lacrimal duct and deposit bacteria in nasopharynx Tears contain a high concentration of lysozyme (effective against gram positive microorganisms Receptors Almost all of biology occurs because recognition Enzymatic action Interactions between cells (cooperation/activation) Communication between cells Innate and adaptive immunity requires it Innate Immune Recognition All multi-cellular organisms are able to recognize and eliminate pathogens Despite their extreme heterogeneity, pathogens share highly conserved molecules, called pathogen-associated molecular patterns (PAMPs) Host cells do not share PAMPs with pathogens PAMPs are recognized by innate immune recognition receptors called pattern-recognition molecules/receptors (PRMs/PRRs) Typical PAMPs Lipopolysaccharides Peptidoglycans Certain nucleotide sequences unique to bacteria Other bacterial components Endogenous Signals Induced by PAMPs Mediate inflammatory cytokines Antigen-presenting cells recognize PAMPs Same APC processes pathogens into specific pathogen-derived antigens and presents them with MHC encoded receptors to T-cells T-cell responds only when presented with both signals Different Effector Cytokines in Response to Different Pathogens (Th1 vs. Th2) Antimicrobial Peptides/Defensins Four hundred peptides described to date Defensins (3- 5-kD, four families in eukaryotes) a-defensins (neutrophils and intestinal Paneth cells) b-defensins (epithelial cells) Insect defensins Plant defensins Defensins appear to act by binding to outer membrane of bacteria, resulting in increased membrane permeability. May also play a role in inflammation and wound repair
Complement System Three pathways now known Classical Alternative Lectin or MBL pathway (binding to mannose- containing carbohydrates) Host cells have complement regulatory proteins on their surface that protect them from spontaneous activation of C3 molecules Inflammatory Mediators in Innate Immunity Cytokines secreted by phagocytes in response to infection include: IL-1 activates vascular endothelium and lymphocytes Increases adhesiveness of leukocytes IL-6 Induces B-cell terminal maturation into Ig-producing plasma cells IL-8 Induces expression of b2 integrin adhesion molecules on neutrophils, leading to neutrophil migration to infection site IL-12 Activates NK cells and induces Th1-cell differentiation IL-18 TNF-a Activates vascular endothelium and increases vascular permeability, leading to accumulation of Ig and complement in infected tissues Other Mediators and Molecules Phagocytes Toxic oxygen radicals Peroxides Nitric oxide (NO) Lipid mediators of inflammation Prostaglandins LTB4 Platelet activating factor Complement component C5a Stimulates mast cells to release histamine, serotonin and LTB4 IL-1, IL-6 and TNF-a Induce acute-phase response in liver Induce fever IL-1 and IL-18 signaling pathways activate NF-kB, important in innate immunity Immune Cells and Innate Immunity Phagocytes Neutrophils Moncyte/macrophage Eosinophils (to a lesser extent) NK cells (large granular lymphocytes) Antibody-dependent cell-mediated cytotoxicity (ADCC) Have two major functions Lysis of target cells Production of cytokines (IFN-g and TNF-a) Act against intracellular pathogens Herpesviruses Leishmania Listeria monocytogenes Act against protozoa Toxoplasma Trypanasoma Immune Cells and Innate Immunity (contd) g/d T cells Two types of T cell receptors One composed of a and b chains (basic T cell antigen receptor) One composed of g and d chains (minor population of T cells) Two groups of g/d T cells One group found in lymphoid tissues One group located in paracellular space between epithelial cells Recognizes unprocessed target antigen in absence of APC help B-1 cells (minor fraction of B cells, do not require T-cell help) Mast cells Located in serosa, under epithelial surfaces and adjacent to blood vessels, nerves and glands Capable of phagocytosis Process and present antigen using MHC class I or II receptors LPS can directly induce release of mast cell mediators Complement (C3a and C5a) induce mast cells to release mediators Chemotaxis, complement activation, inflammation TNF-a secreted by mast cells results in neutrophil influx into infected site
Summary of Innate Immunity External and mechanical barriers Receptors for pathogen motifs Soluble antimicrobial proteins Pattern of cytokines produced influences adaptive response