1. The Rockin’ Immune System Honors Biology

2. Vocabulary n Pathogen – infecting agent n Antigen – molecular “flag” studded into pathogens n Lymphocytes – specialized immune cells n Antibody – chemical “scouts” produced by lymphocytes to recognize antigens n Phagocyte/Macrophage – garbage pickup and disposal for the body

3. The Immune Response Immunity: “Free from burden”. Ability of an organism to recognize and defend itself against specific pathogens or antigens. Immune Response: Third line of defense. Involves production of antibodies and generation of specialized lymphocytes against specific antigens. Antigens are the molecules from a pathogen or foreign organism which provoke the specific immune response.

4. Active and Passive Immunity Passive immunity n B and T (lymphocyte) cells are not activated n The antigen doesn’t have to be encountered n Skin, mucus, digestive acids and enzymes are examples of things which provide passive immunity

5. Active and Passive Immunity Active immunity n Lymphocytes are activated by antigens on the surface of pathogens n Natural immunity is acquired due to infection n Artificial immunity is acquired through vaccination n Takes time for enough B and T cells to be produced to mount an effective response.

6. The Immune System is the Third Line of Defense Against Infection

7. Innate or Genetic Immunity: Immunity an organism is born with. u Genetically determined. u May be due to lack of receptors or other molecules required for infection. F Innate human immunity to canine distemper. F Immunity of mice to polio (a virus). Acquired Immunity:Immunity that an organism develops during lifetime. u Not genetically determined. u May be acquired naturally or artificially. F Development of immunity to measles in response to infection or vaccination.

8. Components of Human Immune System

9. Antibodies are Proteins that Recognize Specific Antigens

10. Antigens u Most are proteins or large carbohydrates from a foreign particle or organism u Microbes: Capsules, cell walls, toxins, viral capsids, flagella, etc. u Nonmicrobes: Pollen, egg white, red blood cell surface molecules, serum proteins, and surface molecules from transplanted tissue.

11. Antigens Epitope: u Small part of an antigen that interacts with an antibody. u Any given antigen may have several epitopes. u Each epitope is recognized by a different antibody.

12. Epitopes: Antigen Regions that Interact with Antibodies

13. Antibodies u Proteins that recognize and bind to a particular antigen with very high specificity. u Made in response to exposure to the antigen. u One virus or microbe may have several antigenic determinant sites, to which different antibodies may bind. u Each antibody has at least two identical sites that bind antigen u Belong to a group of proteins called immunoglobulins (Igs).

14. Antibody Structure

15. B Cells Produce Antibodies u B cells develop from stem cells in the bone marrow of adults (liver of fetuses). u Clonal Selection: When a B cell encounters an antigen it recognizes, it is stimulated and divides into many clones called plasma cells, which actively secrete antibodies. u Each B cell produces antibodies that will recognize only one antigenic determinant.

16. Clonal Selection of B Cells is Caused by Antigenic Stimulation

17. Immunity (Continued) Apoptosis u Programmed cell death (senescence) u Human body makes 100 million lymphocytes every day. If an equivalent number doesn’t die, one will develop leukemia. u B cells that do not encounter stimulating antigen will self-destruct and send signals to phagocytes to dispose of their remains. u Many virus infected cells will undergo apoptosis, to help prevent spread of the infection.

18. Immunity (Continued) Clonal Selection u Clonal Selection: B cells (and T cells) that encounter stimulating antigens will proliferate into a large group of cells. u Why don’t we produce antibodies against our own antigens? u Clonal Deletion: B and T cells that react against self antigens appear to be destroyed during fetal development. F This process is poorly understood because it is difficult to study.

19. Consequences of Antigen-Antibody Binding Antigen-Antibody Complex: Formed when an antibody binds to an antigen it recognizes. Affinity: A measure of binding strength. 1. Agglutination: Antibodies cause antigens (microbes) to clump together. F IgM (decavalent) is more effective that IgG (bivalent). F Hemagglutination: Agglutination of red blood cells. Used to determine ABO blood types and to detect influenza and measles viruses. 2. Antigen (microbe) is covered with antibodies that enhances its ingestion and lysis by phagocytic cells.

20. Consequences of Antibody Binding

21. Immunity (Continued) 3. Neutralization: IgG inactivates viruses by binding to their surface and neutralize toxins by blocking their active sites. 4. Antibody-dependent cell-mediated cytotoxicity: Used to destroy large organisms (e.g.: worms). Target organism is coated with antibodies and bombarded with chemicals from nonspecific immune cells. 5. Complement Activation: Both IgG and IgM trigger the complement system which results in cell lysis and inflammation.

22. Consequences of Antibody Binding

23. Immunological Memory Pattern of Antibody Levels During Infection Primary Response: u After initial exposure to antigen, no antibodies are found in blood for several days. u A gradual increase of antibodies in blood is observed. u Most B cells become plasma cells, but some B cells become long living memory cells. u Gradual decline of antibodies follows.

24. Immunological Memory (Continued) Secondary Response: u Subsequent exposure to the same antigen displays a faster and more intense antibody response. u Increased antibody response is due to the existence of memory cells, which rapidly produce plasma cells upon antigen stimulation.

25. Antibody Response After Exposure to Antigen

26. T Cells and Cell Mediated Immunity Cellular Components of Immunity: u T cells are key cellular component of immunity. u T cells have an antigen receptor that recognizes and reacts to a specific antigen (T cell receptor). u T cell receptor only recognize antigens combined with antibodies u Clonal selection increases number of T cells.

27. T Cells Only Recognize Antigens Associated with Antibodies on Cell Surfaces

28. T Cells and Cell Mediated Immunity Types of T cells 1. T Helper (T H ) Cells: Central role in immune response. F Recognize antigen on the surface of antigen presenting cells (e.g.: macrophage). F Activate macrophages F Activate Cytotoxic T-Cells F Stimulate B cells to produce antibodies.

29. Central Role of Helper T Cells

30. Types of T cells (Continued) 2. Cytotoxic T Cells: Destroy target cells. F Recognize antigens on the surface of all cells: Kill host cells that are infected with viruses or bacteria.Kill host cells that are infected with viruses or bacteria. Recognize and kill cancer cells.Recognize and kill cancer cells. Recognize and destroy transplanted tissue.Recognize and destroy transplanted tissue. F Release protein which punctures invading target cell, causing lysis of infected cells. F Undergo apoptosis when stimulating antigen is gone.

31. Cytotoxic T Cells Lyse Infected Cells

32. Nonspecific Cellular Components 1. Activated Macrophages: Stimulated phagocytes. F Stimulated by ingestion of antigen F Larger and more effective phagocytes. F Enhanced ability to eliminate intracellular bacteria, virus-infected and cancerous cells. 2. Natural Killer Cells: F Lymphocytes that destroy virus infected and tumor cells. F Not specific. Don’t require antigen stimulation. F Not phagocytic, but must contact cell in order to lyse it.

33. Phagocytosis

34. Immunity Review 1. Antibody Production T-Dependent Antigens: u Antibody production requires assistance from T helper cells. u A macrophage cells ingest antigen and presents it to T H cell. u T H cell stimulates B cells specific for antigen to become plasma cells. u Antigens are mainly proteins on viruses, bacteria, foreign red blood cells, and hapten-carrier molecules. T-Independent Antigens: u Antibody production does not require assistance from T cells. u Antigens are mainly polysaccharides or lipopolysaccharides with repeating subunits (bacterial capsules). u Weaker immune response than for T-dependent antigens.

35. More Immunity Review 2. Antibody Dependent Cell Mediated Cytotoxicity u Target cell is covered with antibodies, leaving portion sticking outwards. u Natural killer and other nonspecific cells that have receptors for region are stimulated to kill targeted cells. u Target organism is lysed by substances secreted by attacking cells. u Used to destroy large organisms that cannot be phagocytosed.

36. Destruction of Large Parasites

37. Overview of the Immune Response

38. What about fevers? n The hypothalamus in the brain works like a thermostat, controlling body temperature n Body induces fever to speed immune response u Some say it also helps reduce pathogenic lifespan n Fever is not disease! It is a symptom

39. Blood Types: Matching Antibodies & Antigens will agglutinate

40. Vaccination A preparation containing antigenic material: n Whole live microorganism n Dead microorganism n Attenuated (harmless) microorganism n Toxoid (harmless form of toxin) n Preparation of harmless pathogen

41. Smallpox Eradication program n Started by WHO in 1956 n Aimed to rid world of smallpox by 1977 n Involved vaccination and surveillance n Over 80% of populations at risk of the disease were vaccinated n After any reported case everyone in the household and 30 surrounding households vaccinated

42. Smallpox Eradication program n Last case of smallpox reported in Somalia in 1977 n World declared free of smallpox in 1980

43. Smallpox Eradication program – why was it successful? n Variola virus stable -> cheap as everyone used same vaccine n Vaccine made from harmless strain of similar virus (vaccinia) n Vaccine could be used at high temperatures n Easy to identify infected people n Smallpox doesn’t lie dormant in body

44. Allergies n When the immune system responds to harmless substances n Allergens – antigenic substances which do no real harm n Allergens include house dust, animal skin, pollen, house dust mite and its feces

46. Allergies n Histamine causes blood vessels to widen and become leaky. n Fluid and white blood cells leave capillaries. n The area of leakage becomes hot, red and inflamed

47. Asthma n Attacks can occur at any time n Genes play a role in who develops asthma n Breathing becomes difficult, sufferers experience wheezing, coughing, a tightness about the chest and shortage of breath. n 1/7 children in UK has asthma, number is increasing. n >1000 people die each year from asthma every year in the UK

48. Asthma n Airways in asthmatics are always inflamed, during an attack this worsens. n Fluid leaks from blood into airways and goblet cells secrete lots of mucus n Airways can become blocked n Muscles surrounding trachea and bronchioles contract which narrows airways further

49. Asthma n Vaccines are being developed to make allergic responses less severe n Designed to desensitise people so they do not produce antibodies to allergens n Genetic tests may be used to screen children and then a vaccine could be given to prevent them developing asthma