1. CAMPBELL BIOLOGY IN FOCUS © 2014 Pearson Education, Inc. Urry Cain Wasserman Minorsky Jackson Reece Lecture Presentations by Kathleen Fitzpatrick and Nicole Tunbridge 35 The Immune System

2. © 2014 Pearson Education, Inc. Overview: Recognition and Response  Pathogens, agents that cause disease, infect a wide range of animals, including humans  The immune system enables an animal to avoid or limit many infections  Innate immunity, general and rapid: phagocytosis, and antimicrobial peptides, natural killer cells, interferons, and the inflammatory response  Adaptive immunity, specific and slower.

3. © 2014 Pearson Education, Inc. Figure 35.1

4. © 2014 Pearson Education, Inc. Figure 35.2 INNATE IMMUNITY (all animals) Recognition of traits shared by broad ranges of pathogens, using a small set of receptors Rapid response Barrier defenses: Skin Mucous membranes Secretions Internal defenses: Phagocytic cells Natural killer cells Antimicrobial proteins Inflammatory response Humoral response: Antibodies defend against infection in body fluids. Cytotoxic cells defend against infection in body cells. Cell-mediated response: ADAPTIVE IMMUNITY (vertebrates only) Recognition of traits specific to particular pathogens, using a vast array of receptors Slower response Pathogens (such as bacteria, fungi, and viruses)

5. © 2014 Pearson Education, Inc. Cellular Innate Defenses  Pathogens entering the mammalian body are subject to phagocytosis  Phagocytic cells recognize groups of pathogens by Toll-like receptors (TLRs)  Each mammalian TLR binds to fragments of molecules characteristic to a set of pathogens

6. © 2014 Pearson Education, Inc. Figure 35.4 VESICLE CpG DNA dsRNA TLR9 TLR3 Innate immune responses TLR5 TLR4 Flagellin Lipopolysaccharide Helper protein PHAGOCYTIC CELL EXTRACELLULAR FLUID

7. © 2014 Pearson Education, Inc.  There are two main types of phagocytic cells in mammals  Neutrophils circulate in the blood and are attracted by signals from infected tissues  Macrophages are found throughout the body  Dendritic cells stimulate development of adaptive immunity in cells that contact the environment (such as skin)  Eosinophils discharge destructive enzymes beneath mucosal surfaces

8. © 2014 Pearson Education, Inc.  Cellular innate defenses in vertebrates also involve natural killer cells  These circulate through the body and detect abnormal cells  They release chemicals leading to cell death, inhibiting the spread of virally infected or cancerous cells  Many cellular innate defenses involve the lymphatic system

9. © 2014 Pearson Education, Inc. Antimicrobial Peptides and Proteins  In mammals, pathogen recognition triggers release of peptides and proteins that attack pathogens or impede their reproduction  Interferons secreted by infected cell provide prevent viruses from infection of other cells and help activate macrophages  The complement system consists of about 30 proteins circulating in blood that are activated by substances on microbe surfaces  Activation can lead to lysis of invading cells

10. © 2014 Pearson Education, Inc. Inflammatory Response  The inflammatory response, such as pain and swelling, is brought about by molecules released upon injury of infection  Mast cells release histamine, which triggers blood vessels to dilate and become more permeable  Activated macrophages and neutrophils release cytokines, signaling molecules that modulate the immune response and promote blood flow to the site of injury or infection

11. © 2014 Pearson Education, Inc. Figure 35.5-3 Pathogen Splinter Macro- phage Capillary Neutrophil Red blood cells Mast cell Signaling molecules 1 Histamines and cytokines released. Capillaries dilate. Movement of fluid 2 Antimicrobial peptides enter tissue. Neutrophils are recruited. Phagocytosis 3 Neutrophils digest pathogens and cell debris. Tissue heals.

12. © 2014 Pearson Education, Inc. Evasion of Innate Immunity by Pathogens  Adaptations have evolved in some pathogens that enable them to avoid destruction by phagocytic cells  Tuberculosis (TB) resists breakdown within lysosomes after being engulfed by a host cell  Mechanisms like this make certain fungi and bacteria substantial pathogenic threats

13. © 2014 Pearson Education, Inc. Concept 35.2: In adaptive immunity, receptors provide pathogen-specific recognition  The adaptive response relies on two types of lymphocytes, or white blood cells  Lymphocytes that mature in the thymus above the heart are called T cells, and those that mature in bone marrow are called B cells

14. © 2014 Pearson Education, Inc. Figure 35.UN01 Antigen receptors Mature B cellMature T cell

15. © 2014 Pearson Education, Inc.  Antigens (bacterial or viral protein) can elicit a response from a B or T cell  Recognition occurs when a B or T cell binds to the antigen, via an antigen receptor  The immune system produces millions of different antigen receptors but the receptors, on a single B cell or T cell are all identical to one another

16. © 2014 Pearson Education, Inc. Figure 35.UN01 Antigen receptors Mature B cellMature T cell

17. © 2014 Pearson Education, Inc. Antigen Recognition by B Cells and Antibodies  Each B cell antigen receptor is a Y-shaped molecule with two identical heavy chains and two identical light chains  The constant (C) regions of the chains vary little among B cells, whereas the variable (V) regions differ greatly  Together, the V regions of the heavy and light chains form an antigen-binding site

18. © 2014 Pearson Education, Inc. Figure 35.6 Antigen- binding site B cell antigen receptor Disulfide bridge Light chain Antigen- binding site Variable regions Constant regions Transmembrane regions Plasma membrane Heavy chains Cytoplasm of B cell B cell V V C C C C V V

19. © 2014 Pearson Education, Inc. Figure 35.7 Antigen- receptor Antibody B cell Antigen Epitope Pathogen (a) B cell antigen receptors and antibodies Antibody C Antibody A Antibody B Antigen (b) Antigen receptor specificity

20. © 2014 Pearson Education, Inc.  Binding of a B cell antigen receptor to an antigen is an early step in B cell activation  This gives rise to cells that secrete a soluble form of the protein called an antibody or immunoglobulin (Ig)  Secreted antibodies are similar to B cell receptors but are not membrane bound Antigen Recognition by B Cells and Antibodies

21. © 2014 Pearson Education, Inc.  Made in the Thymus and  Each T cell receptor consists of two different polypeptide chains (called  and  )  The tips of the chain form a variable (V) region; the rest is a constant (C) region  The V regions of the  and  chains together form an antigen-binding site Antigen Recognition by T Cells

22. © 2014 Pearson Education, Inc. Figure 35.8 Antigen- binding site T cell antigen receptor Disulfide bridge T cell Cytoplasm of T cell  chain  chain Variable regions Constant regions Transmembrane region Plasma membrane VV CC

23. © 2014 Pearson Education, Inc.  T cells bind only to antigen fragments displayed or presented on a host cell  MHC (major histocompatibility complex) molecules are host proteins that display the antigen fragments on the cell surface Antigen Recognition by T Cells

24. © 2014 Pearson Education, Inc.  In infected cells, antigens are cleaved into smaller peptides by enzymes  MHC molecules bind and transport the antigen fragments to the cell surface, a process called antigen presentation  A T cell can then bind both the antigen fragment and the MHC molecule  This interaction is necessary for the T cell to participate in the adaptive immune response Antigen Recognition by T Cells

25. © 2014 Pearson Education, Inc. Figure 35.9 Host cell Displayed antigen fragment MHC molecule Antigen fragment Pathogen T cell T cell antigen receptor

26. © 2014 Pearson Education, Inc. B Cell and T Cell Development  The adaptive immune system has four major characteristics  Diversity of lymphocytes and receptors  Self-tolerance; lack of reactivity against an animal’s own molecules  Proliferation of B and T cells after activation  Immunological memory

27. © 2014 Pearson Education, Inc. Generation of B and T Cell Diversity  By combining variable elements, the immune system assembles a diverse variety of antigen receptors  The capacity to generate diversity is built into the structure of Ig genes  Many different chains can be produced from the same gene by rearrangement of the DNA  Rearranged DNA is transcribed and translated and the antigen receptor formed

28. © 2014 Pearson Education, Inc. Figure 35.10 pre-mRNA mRNA DNA of differentiated B cell DNA of undifferentiated B cell RNA processing Transcription of permanently rearranged, functional gene Recombination deletes DNA between randomly selected V segment and J segment Functional gene 1 2 3 4 Translation Light-chain polypeptide Variable region Constant region B cell Antigen receptor V C C Cap V 39 J5J5 Poly-A tail V V V V C CC C C V 39 J5J5 Intron C V 39 J5J5 Intron V 38 V 37 V 39 V 38 V 40 V 37 J5J5 J4J4 J3J3 J2J2 J1J1 Intron C

29. © 2014 Pearson Education, Inc. Figure 35.10a DNA of undifferentiated B cell V 39 V 38 V 40 V 37 J5J5 J4J4 J3J3 J2J2 J1J1 Intron DNA of differentiated B cell pre-mRNA Transcription of permanently rearranged, functional gene Recombination deletes DNA between randomly selected V segment and J segment Functional gene C V 39 V 38 V 37 J5J5 Intron C C V 39 J5J5 21

30. © 2014 Pearson Education, Inc. Figure 35.10b pre-mRNA Intron C V 39 J5J5 mRNA RNA processing C Cap V 39 J5J5 Poly-A tail Translation Light-chain polypeptide Variable region Constant region B cell Antigen receptor V C V V V V C C C C 43

31. © 2014 Pearson Education, Inc. Origin of Self-Tolerance  Antigen receptors are generated by random rearrangement of DNA  As lymphocytes mature in bone marrow or the thymus, they are tested for self-reactivity  Some B and T cells with receptors specific for the body’s own molecules are destroyed by apoptosis, or programmed cell death  The remainder are rendered nonfunctional

32. © 2014 Pearson Education, Inc.  Once activated, a B or T cell undergoes multiple cell divisions to produce a clone of identical cells (called clonal selection)  Two types of clones are produced  Short-lived activated effector cells that act immediately against the antigen  Long-lived memory cells that can give rise to effector cells if the same antigen is encountered again

33. © 2014 Pearson Education, Inc. Figure 35.11 B cells that differ in antigen specificity Antigen Antigen receptor Antibody Plasma cellsMemory cells

34. © 2014 Pearson Education, Inc.  Immunological memory is responsible for long-term protections against diseases, due to a prior infection  The first exposure to a specific antigen represents the primary immune response  During this time, selected B and T cells give rise to their effector forms  In the secondary immune response, memory cells facilitate a faster, stronger, and longer response  Immunological memory can span many decades Immunological Memory

35. © 2014 Pearson Education, Inc. Figure 35.12 Primary immune response to antigen A Secondary immune response to antigen A Antibodies to A Antibodies to B 10 1 10 3 10 4 10 0 0714212835424956 Primary immune response to antigen B Antibody concentration (arbitrary units) Exposure to antigen A Exposure to antigens A and B Time (days) 10 2

36. © 2014 Pearson Education, Inc. Concept 35.3: Adaptive immunity defends against infection of body fluids and body cells  B and T lymphocytes produce a humoral immune response and a cell-mediated immune response  In the humoral immune response, antibodies help neutralize or eliminate toxins and pathogens in the blood and lymph  In the cell-mediated immune response specialized T cells destroy infected host cells

37. © 2014 Pearson Education, Inc. Helper T Cells: A Response to Nearly All Antigens  A type of T cell called a helper T cell triggers both the humoral and cell-mediated immune responses  An antigen must be displayed on the surface of an antigen-presenting cell and bind specifically to the antigen receptor of a T cell  Antigen-presenting cells have class I and class II MHC molecules on their surfaces

38. © 2014 Pearson Education, Inc.  Antigen-presenting cells are recognized based on their class II MHC molecules  Antigen receptors on the surface of helper T cells bind to the antigen and the class II MHC molecule  Signals are then exchanged between the two cells  The helper T cell is activated, proliferates, and forms a clone of helper T cells, which then activate the appropriate B cells

39. © 2014 Pearson Education, Inc. Figure 35.13 Antigen- presenting cell Antigen fragment Class II MHC molecule Accessory protein (CD4) Antigen receptor Helper T cell Pathogen Cytokines B cell 1 2 3 3 Cytotoxic T cell Cell-mediated immunity Humoral immunity

40. © 2014 Pearson Education, Inc. Cytotoxic T Cells: A Response to Infected Cells  Cytotoxic T cells are the effector cells in the cell- mediated immune response  Cytotoxic T cells recognize fragments of foreign proteins produced by infected cells and possess an accessory protein that binds to class I MHC molecules  The activated cytotoxic T cell secretes proteins that disrupt the membranes of target cells and trigger apoptosis Animation: Cytotoxic T Cells

41. © 2014 Pearson Education, Inc. Figure 35.14-1 Antigen fragment Class I MHC molecule Accessory protein Antigen receptor Cytotoxic T cell Infected cell 1

42. © 2014 Pearson Education, Inc. Figure 35.14-2 Antigen fragment Class I MHC molecule Accessory protein Antigen receptor Cytotoxic T cell Infected cell 1 Pore 2 Perforin Granzymes

43. © 2014 Pearson Education, Inc. Figure 35.14-3 Antigen fragment Class I MHC molecule Accessory protein Antigen receptor Cytotoxic T cell Infected cell 1 Pore 2 Perforin Granzymes Released cytotoxic T cell Dying infected cell 3

44. © 2014 Pearson Education, Inc. B Cells and Antibodies: A Response to Extracellular Pathogens  The humoral response is characterized by secretion of antibodies by clonally selected B cells  Activation of B cells involves helper T cells and proteins on the surface of pathogens  In response to cytokines from helper T cells and an antigen, a B cell proliferates and differentiates into memory B cells and antibody-secreting effector cells called plasma cells

45. © 2014 Pearson Education, Inc. Figure 35.15-1 Helper T cell Antigen fragments Pathogen CD4 Antigen- presenting cell Antigen receptor 1 MHC

46. © 2014 Pearson Education, Inc. Figure 35.15-2 Helper T cell Antigen fragments Pathogen CD4 Antigen- presenting cell Antigen receptor MHC B cell Cytokines Activated helper T cell 2 1

47. © 2014 Pearson Education, Inc. Figure 35.15-3 Helper T cell Antigen fragments Pathogen CD4 Antigen- presenting cell Antigen receptor MHC B cell Cytokines Activated helper T cell 2 1 3 Plasma cells Secreted antibodies Memory B cells

48. © 2014 Pearson Education, Inc.  Antibodies do not kill pathogens; instead, they mark pathogens for destruction  In neutralization, antibodies bind to viral surface proteins, preventing infection of a host cell  Antibodies may also bind to toxins in body fluids and prevent them from entering body cells

49. © 2014 Pearson Education, Inc.  Both the humoral and cell-mediated responses can include primary and secondary immune responses  Memory cells enable the secondary response Summary of the Humoral and Cell-Mediated Immune Responses

50. © 2014 Pearson Education, Inc. Figure 35.16 B cell Helper T cell Antigen- presenting cell Engulfed by Antigen (1st exposure) Humoral (antibody-mediated) immune response Cell-mediated immune response Key Stimulates Gives rise to Cytotoxic T cell Memory helper T cell Memory cytotoxic T cells Memory B cells Antigen (2nd exposure) Active cytotoxic T cells Defend against intracellular pathogens and cancer Defend against extracellular pathogens Plasma cells Secreted antibodies

51. © 2014 Pearson Education, Inc. Figure 35.16a B cell Helper T cell Antigen- presenting cell Engulfed by Antigen (1st exposure) Humoral (antibody-mediated) immune response Cell-mediated immune response Key Stimulates Gives rise to Cytotoxic T cell

52. © 2014 Pearson Education, Inc. Figure 35.16b B cell Helper T cell Humoral (antibody-mediated) immune response Cell-mediated immune response Cytotoxic T cell Key Stimulates Gives rise to Memory helper T cell Memory cytotoxic T cells Memory B cells Antigen (2nd exposure) Active cytotoxic T cells Defend against intracellular pathogens and cancer Defend against extracellular pathogens Plasma cells Secreted antibodies

53. © 2014 Pearson Education, Inc. Active and Passive Immunization  Active immunity occurs naturally when a pathogen infects the body  Passive immunity provides immediate, short-term protection  It is conferred naturally when antibodies cross the placenta from mother to fetus or pass from mother to infant in breast milk

54. © 2014 Pearson Education, Inc.  Both active and passive immunity can be induced artificially  Active immunity is induced when antigens are introduced into the body in vaccines  Passive immunity can be conferred artificially by injecting antibodies into a nonimmune person

55. © 2014 Pearson Education, Inc.  Acquired immunodeficiency syndrome (AIDS) is caused by HIV (human immunodeficiency virus), which both attacks and escapes the immune system  It infects helper T cells with high efficiency  It escapes the immune system through its high mutation rate, which reduces the ability of the immune system to eliminate the infection  It also can undergo latency  People with AIDS are highly susceptible to infections and cancers that a healthy immune system would normally defeat