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Chapter 39: Immunity

Chapter 39: Immunity. Fig. 39-1, p.678. Fig. 39-2, p.679. Three Lines of Defense. Barriers at body surfaces Nonspecific responses Immune responses. Cells Involved in Immune Responses. basophil. mast cell. eosinophil. neutrophil. NK cell. B lymphocyte. T lymphocyte. Fig. 39-3a, p.681.

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Chapter 39: Immunity

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  1. Chapter 39: Immunity

  2. Fig. 39-1, p.678

  3. Fig. 39-2, p.679

  4. Three Lines of Defense • Barriers at body surfaces • Nonspecific responses • Immune responses

  5. Cells Involved in Immune Responses basophil mast cell eosinophil neutrophil NK cell B lymphocyte T lymphocyte Fig. 39-3a, p.681

  6. Cells Involved in Immune Responses dendritic cell macrophage Fig. 39-3b, p.681

  7. Fig. 39-4, p.680

  8. Barriers at Body Surface • Intact skin and mucous membranes • Lysozyme • Normal bacterial flora • Flushing effect and low pH of urine

  9. Barriers Against Infectious Agents Fig. 39-6, p.683

  10. Barriers Against Infectious Agents Fig. 39-7, p.683

  11. Nonspecific Responses • Lymph nodes trap and kill pathogens • Natural killer cells attack a range of targets • Inflammation

  12. Complement System • Plasma proteins that take part in both specific and nonspecific response • Activation of one triggers cascade of reactions that activate others

  13. Attack Complexes lipid bilayer of pathogen antibody activated complement bacterial pathogen Cascade Reactions Formation of Attack Complexes Lysis of Target Activation

  14. Acute Inflammation • Nonspecific response to foreign invasion, tissue damage, or both • Destroys invaders, removes debris, and prepares area for healing • Characterized by redness, swelling, warmth, and pain

  15. Inflammation • Mast cells release histamine • Capillaries dilate and leak • Complement proteins attack bacteria • White cells attack invaders and clean up Figure 39.9Page 685

  16. Features of Immune Responses • Self/nonself recognition • Specificity • Diversity • Memory

  17. Memory and Effector Cells • When a B or T cell is stimulated to divide, it produces more than one cell type • Memory cells - set aside for future use • Effector cells - engage and destroy the current threat

  18. Steps in Immune Response • Recognition of an antigen • Rounds of cell division that form huge populations of lymphocytes • Specialization of lymphocytes into effector and memory cells that have receptors for one kind of antigen

  19. Key Components of Immune Response • MHC markers • Antigen-presenting cells • T cells • B cells • Natural killer cells

  20. Formation of Antigen-MHC Complex antigen fragments MHC molecule antigen-MHC complex

  21. Antigens • “Nonself” markers on foreign agents and altered body cells such as tumors • Trigger division of B and T cells

  22. Interactions Between Responses

  23. Lymphocyte Battlegrounds • Lymph nodes filter antigens from body fluids • Macrophages, dendritic cells, B and T cells in nodes and spleen mount a defense Figure 39.12Page 687

  24. Antibody Structure • Consists of four polypeptide chains • Certain parts of each chain are variable; impart antigen specificity antigen binding site variable region constant region Figure 39.13aPage 688

  25. signal reception signal transduction cellular response Antibody-Mediated Immune Response Cell-Mediated Immune Response antigen-presenting cells naive B cells + antigen + complement naive helper T cells activated B cells naive cytotoxic T cells effector helper T cells + memory helper T cells effector B cells + memory B cells effector cytotoxic T cells + memory cytotoxic cells Fig. 39-11, p.687

  26. Antibody-Mediated Response • Carried out by B cells • Targets are intracellular pathogens and toxins • Antibodies bind to target and mark it for destruction by phagocytes and complement

  27. antigen Clonal Selection • Only the B cell with antigen-receptor that matches antigen is stimulated to divide • Mitosis yields many cells with that receptor clonal population of B cells Figure 39.15Page 690

  28. Immunological Memory • Memory cells specific for an antigen are quickly activated to divide upon subsequent exposure to that antigen Primary Immune Response: naïve T or B cell effector cells memory cells Secondary Immune Response: effector cells memory cells Figure 39.15Page 690

  29. Primary and Secondary Immune Response Fig. 39-16, p.690

  30. Antibody-Mediated Response • B cell becomes antigen-presenting cell • Helper T cell binds to antigen-MHC complex • Interleukins stimulate B cell division and differentiation • Effector cells secrete antibodies antigen naïve B cell MHC molecule antigen- MHC complex helper T cell antigen- presenting B cell interleukins memory B cell antibody effector B cell

  31. bacterium dendritic cell complement naive B cell naive T cell antigen-presenting cell cytokines memory helper T cell effector helper T cell B cell effector B cell memory B cell Stepped Art Fig. 39-17, p.691

  32. virus particle (red) infecting a body cell (yellow) dendritic cell antigen-MHC complex naive cytotoxic T cell naive helper T cell antigen-presenting cell effector cytotoxic T cell memory cytotoxic T cell effector cytotoxic T cell cytokines memory helper T cell effector helper T cell activated cytotoxic T cell Stepped Art Fig. 39-18, p.692

  33. Cell-Mediated Response another macrophage one macrophage • Carried out by T cells • Stimulated by antigen-presenting macrophages • Main target is antigen-presenting body cells (cells with intracellular pathogens) or tumor cells interleukins cytotoxic T cell helper T cell interleukins infected body cell

  34. Cytotoxic T Cell cytotoxic T-cell tumor cell Fig. 39-19, p.693

  35. Organ Rejection • Cytotoxic T cells can contribute to rejection • They recognize a portion of the donor cell’s MHC complex as self, view a portion as foreign • Treat the combination as an antigen-MHC complex and attack donor cells

  36. Immunization • Process that promotes immunity • Active immunization - • Antigen-containing material is injected • Confers long-lasting immunity • Passive - • Purified antibody is injected • Protection is short lived

  37. Vaccines Fig. 39-21a, p.694

  38. Vaccines RECOMMENDED VACCINES RECOMMENDED AGES Hepatitis B Hepatitis B booster 1 Hepatitis B booster 2 Hepatitis B assessment DTP (Diphtheria; Tetanus; and Pertussin, or whooping cough) DTP booster 1 DTP booster 2 DT HiB (Hemophilus influenzae) HiB booster Polio Polio booster 1 Polio booster 2 MMR (Measles, Mumps, Rubella) MMR booster MMR assessment Pneumococcal Pneumococcal booster 1 Pneumococcal booster 2 Varicella Varicella assessment Hepatitis A (in selected areas Birth–2 months 1–4 months 6–18 months 11–12 years 2, 4, and 6 months 15–18 months 4–6 years 11–16 years 2, 4, and 6 months 12–15 months 2 and 4 months 6–18 months 4–6 years 12–15 months 4–6 years 11–12 years 2, 4, and 6 months 12-15 months 1-18 years 12–18 months 11–12 years 1-12 years Fig. 39-21b, p.694

  39. Allergies • Immune reaction to a harmless substance • Genetic predisposition • IgE responds to antigen by binding to mast cells and basophils • These cells secrete the substances that cause symptoms

  40. Fig. 39-22a, p.694

  41. Fig. 39-22b, p.694

  42. AIDS • Combination of disorders that follows infection with HIV • Includes • Yeast (Candida) infections • Pneumocystis pneumonia • Karposi’s sarcoma

  43. Global Cases of AIDS/HIV

  44. HIV Life Cycle reverse transcriptase viral genes are integrated into the host DNA DNA is transcribed viral RNA enters cell host cell strands of DNA (two) viral RNA reverse transcription of viral RNA viral proteins viral DNA budding core proteins (two layers) integrase

  45. T Cell Decline • Release of new viral particles kills the host T cell • The body is constantly making new T cells, but cannot outpace the rate of destruction • As infection proceeds, T cell numbers inevitably decline

  46. Effect of T Cell Decline • CD4 helper T cells play a vital role in immune function • They are required for both cell-mediated and antibody-mediated immunity • Infected individual becomes vulnerable to other infections, which eventually result in death

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