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Introduction to Immunology

Introduction to Immunology. By Dr. Nabil El Aila Assistant Professor of Medical Microbiology Medical Technology Department Al -Aqsa University. Immunity. 1 . Immunity : : Meaning the state of protection from infectious disease .

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Introduction to Immunology

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  1. Introduction to Immunology By Dr. Nabil El Aila Assistant Professor of Medical Microbiology Medical Technology Department Al -Aqsa University

  2. Immunity 1.Immunity: : Meaning the state of protection from infectious disease. In 430BC, a plaque in Athens, Those who recovered from the plaque would not contact the disease a second time. 2. Agents: microorganisms (viruses, bacteria etc) and their products, foods, chemicals, pollen, tumor cells, etc. 3.Immune system: immune tissues and organs, immune cells, immune molecules 4.Immune response:collective and coordinated response to the introduction of foreign substances. 5.Immunology:study the structure of immune system and its functions.

  3. Immune Response • Innate immune response natural immune response non-specific immune response • Adaptive immuneresponse acquired immune response specific immune response

  4. The innate and adaptive immune response

  5. Adaptive immune response

  6. Innate vs. Adaptive Immune • Innate: structural defenses; responds to nonspecific foreign substances • First line: externalsurface epithelium & membranes • Second line: internal defenses: inflammatory processes – antimicrobial proteins, phagocytes, etc.

  7. Innate vs. Adaptive Immune • Adaptive: responds to specific foreign substances • Innate & adaptive mechanisms work together

  8. Innate, Defenses

  9. Innate, Surface Defenses • Skin • physical barrier to microbes • Keratin resistant to most bacterial enzymes & toxins • secretions are acidic pH 3-5 • Mucosa • physical barrier & produces a variety of protective chemicals • Gastric mucosa • very acidic & produces proteolytic enzymes • Saliva & lacrimal fluid contain lysozyme • Mucous • traps bacteria & moves them away from epithelial surface

  10. LACRIMAL APPARATUS.

  11. CILIARY ESCALATOR.

  12. Innate, Defenses

  13. Innate, Internal Defenses • Based on recognition of surface carbohydrates (glycocalyx) • Glycocalyx is recognized as “self” or “non-self”

  14. Innate, Internal Defenses • Phagocytes • Macrophages: derived from monocytes • Free Macrophages: roam through tissues • Fixed Macrophages: Kupffer cells (liver) & microglia cells (brain) Ingest cellular debris, foreign material, bacteria, fungi • Neutrophils: ingest pathogens • Eosinophils: weakly phagocytic of pathogens. Attack parasites (degranulation) • Mast Cells: phagocytic of various bacteria

  15. Innate, Internal Defenses • Phagocytic mechanisms: • Adherence: cell binds to invader • Aided by opsonization (a chemical process that enhances binding via complement & antibodies) • Ingestion: formation of phagolysosomes • Respiratory Bursts: merge phagosome with lysosome & flood phagolysosome with free radicals (macrophage) • Defensins: proteins that crystallize out of solution & pierce pathogen membranes (neutrophils)

  16. Mechanism of Phagocytosis Figure 21.2

  17. Innate, Defenses

  18. Innate, Internal Defenses • Natural Killer Cells: • Small population of large granular lymphocytes • Non specific for “non-self” • Not phagocytic: attack is by release of perforins that perforate the target cell plasma membrane. • Shortly after perforation the target nucleus disintegrates. • Release chemicals that enhance the inflammatory response

  19. Innate, Defenses

  20. Innate, Internal Defenses: Inflammation • tissue response to injury • Triggered by injury – trauma, heat, chemical irritation, infection, etc. • Beneficial effects • Prevents spread of injury • Disposes of cellular debris & pathogens • Promotes repair

  21. Innate, Internal Defenses: Inflammation • cardinal signs of inflammation • Redness • Heat • Swelling • Pain • (functional impairment Rigon)

  22. Innate, Internal Defenses: Inflammation • Inflammatory response: signs are associated with vasodilation & increased vascular permeability • Dilation: redness, heat • Permeability: edema, (increased pressure) pain • Pain also associated with bacterial toxins & some mediators (kinins, PGs)

  23. Innate, Internal Defenses: Inflammatory Response • Mechanisms causing vasodilation & vascular permeability • Injured cells release inflammatory mediators • Histamines • Kinins • Prostaglandins • Complement • Cytokines (also activated by receptors on macrophages in response to microbial glycocalyx)

  24. Innate, Internal Defenses: Inflammatory Response • Edema • Dilutes harmful substances • Provides nutrients (& O2) for repair • Enhances entry of clotting protein • Epithelial breaches also stimulate b-defensin release from epithelial cells

  25. Events in Inflammation Figure 21.3

  26. Innate, Internal Defenses: Inflammatory Response • Phagocyte mobilization: infiltration of damaged area by neutrophils & macrophages

  27. Innate, Internal Defenses: Inflammatory Response • Leukocytosis: leukocytosis inducing factors released by injured cells promote rapid release of WBCs from marrow • Margination: increased vascular permeability causes decreased fluid in vessels; blood flow slows & neutrophils are able to move to vessel margins. Here endothelial markers (CAMs) allow neutrophils to cling to vessel walls (pavementing).

  28. Innate, Internal Defenses: Inflammatory Response • Diapedesis: neutrophils migrate through capillary walls • Chemotaxis– inflammatory chemicals attract neutrophils to move up the chemical concentration gradient (neutrophils respond first) • As the process continues, monocytes diapedes into the area & become macrophages. With chronic inflammation, macrophages predominate

  29. Inflammatory Response:Phagocytic Mobilization Figure 21.4

  30. Innate, Internal Defenses: Inflammatory Response • Macrophages clean up cellular debris & pathogens • If pathogens were associated with the injury, activation of the complement cascade occurs & elements of adaptive immunity join the process

  31. Innate, Internal Defenses • Viral replication – (viruses lack metabolic processes) Viruses release nucleic acid (RNA or DNA) into cytoplasm. The information on the nucleic acid is incorporated into the cell’s DNA. Normal cellular mechanisms then produce viral structural components. Multiple new viral particles are produced & released from the cell (sometimes killing the cell)

  32. Innate, Internal Defenses • Antiviral proteins: interferon & complement • Interferon: some cells produce & release interferons (IFNs) when invaded by virus • Released interferons stimulate nearby cells to produce proteins (PKR) that interfere with viral replication by disrupting protein synthesis & the ribosome • Not virus specific.

  33. Interferon (IFN) Figure 21.5

  34. Innate, Internal Defenses • Complement – a group of plasma proteins (20) that are activated in the presence of foreign substances • Complement activation enhances & amplifies inflammation • Bacteria & some other cell types are lysed by complement activation • Complement activation enhances both innate & adaptive defenses

  35. Innate, Internal Defenses • Complement activation pathways • Classical pathway: requires antibodies • Antibodies bind to target (antigen) • Complement protein C1 binds to the antibody-antigen complex (complement fixation) • Alternative pathway: complement factors interact with microorganism glycocalyx • Both pathways lead to a cascade of protein activation, leading to activation of C3

  36. Innate, Internal Defenses; Complement Figure 21.6

  37. Innate, Internal Defenses • C-reactive proteins (CRP) produced by the liver in response to inflammatory molecules can activate the classical pathway by binding to membrane & activating C1. Also participates in opsonization. • Fever – a systemic response to infection. Leukocytes & macrophages release pyrogens that raise the hypothalamic “set point” for temperature

  38. ADAPTIVE DEFENSES • ADAPTIVE DEFENSES • Innate & adaptive mechanisms work together in a cohesive fashion

  39. Adaptive Defenses: Characteristics • Specificity: directed at specific targets • Systemic: not restricted to initial site of infection / invasion • Memory: after initial exposure & activation, a more rapid & more vigorous response is made to subsequent exposures to pathogens • (secondary response)

  40. Adaptive Defenses: Components • Humoral Immunity: (antibody mediated immunity) provided by antibodies floating free in body fluids • Cell mediated immunity: • lymphocytes directly attack specific invaders by lysis or indirect attack by initiating inflammation and/or activating other lymphocytes & macrophages

  41. Adaptive, Humoral Immunity • Antigen = any substance that can mobilize the immune system & provoke an immune response* *Humoral and/or cell mediated

  42. Adaptive, Humoral Immunity • Complete antigens (proteins, nucleic acids, lipids, polysaccharides): • Immunogenicity: the ability to stimulate specific lymphocytes & specific antibodies • Reactivity: the ability to react with activated lymphocytes & antibodies • Hapten (an incomplete antigen): a smaller molecule that is not immunogenic until attached to proteins

  43. Adaptive, Humoral Immunity • Antigenic determinants: sites on an antigenic molecule that are immunogenic • Epitope • Major Histocompatibility Complex (MHC): cell surface glycoproteins associated with self recognition

  44. Adaptive Immune System: Cells • Lymphocytes • T-cells • B-cells • Antigen Presenting Cells (APCs)

  45. Adaptive Immune System: Cells • Lymphocytes: initially uncommitted • T-cells: are sorted in the Thymus • Positive selection: recognize MHC survive • Negative selection: react against to self-antigens on MHC killed • 2% of initial T-cell precursors • T-cells manage the immune response • B-cells: are sorted in the marrow by an incompletely understood process

  46. Adaptive Immune System: Cells • Immunocompetence: as T- or B-cells mature they become immunocompetent, they display receptors on their cell membrane for a specific antigen. • All of the receptors on one cell are identical; immunity depends upon genetic coding for appropriate receptors.

  47. Adaptive Immune System: Cells • Antigen Presenting Cells (APCs) • APCs ingest foreign material, then present antigenic fragments on their cell surface where they are recognized by T-cells • T-cells: respond to antigen only if it is displayed on plasma membrane. • APCs: Macrophages & B lymphocytes • Interactions between APCs & lymphocytes & lymphocyte-lymphocyte interactions are critical to immune response

  48. Adaptive, Humoral response • Humoral response (clonal selection) • B-cells: Antigen challenge to naïve immunocompetent B-cell • Antigen binds to B-cell receptors & form cross-links between receptors • Cross linked antigen-receptor complex undergoes endocytosis; B-cell presents to T-cell

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