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Immune system Haixu Tang School of Informatics. Human lymphoid organs.

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Presentation on theme: "Immune system Haixu Tang School of Informatics. Human lymphoid organs."— Presentation transcript:

1 Immune system Haixu Tang School of Informatics

2 Human lymphoid organs

3 Lymphocytes are required for adaptive immune responses to foreign antigens

4 Innate immune system helps activate the adaptive immune system

5 The development and activation of T and B cells

6 The clonal selection theory

7 Primary and secondary antibody responses

8 Cellular basis of immunological memory

9 Induction of immunological tolerance

10 B cell activation

11 Innate and adaptive immune responses

12 An antibody molecule

13 Antibody-antigen interactions

14 The hinge region of an antibody molecule

15 A pentameric IgM molecule

16 Antibody-activated phagocytosis

17 There Are Five Classes of Heavy Chains ● IgM, which has μ heavy chains, is always the first class of antibody made by a developing B cell; ● After leaving the bone marrow, the B cell starts to produce cell- surface IgD molecules as well, with the same antigen-binding site as the IgM molecules. ● The major class of immunoglobulin in the blood is IgG, which is a four-chain monomer produced in large quantities during secondary immune responses; ● IgA is the principal class of antibody in secretions, including saliva, tears, milk, and respiratory and intestinal secretions; ● The tail region of IgE molecules, which are four-chain monomers, binds with unusually high affinity (Ka ~ 1010 liters/mole) to yet another class of Fc receptors;

18 Antigen binding to antibody

19 Constant and variable regions

20 The gene of an antibody heavy chain

21 3D structure of antibody

22 Antigen-binding sites of antibodies

23 DNA is rearranged during B cell development

24 The V-J joining process

25 The human heavy-chain gene- segment pool

26 The four main mechanisms of antibody diversification

27 Antibody gene-pool selection in B cell development

28 The two main classes of adaptive immune responses

29 DNA rearrangement that occurs in class switch recombination

30 T cell responses differ from B cell responses in two crucial ways ● T cells are activated by foreign antigen to proliferate and differentiate into effector cells only when the antigen is displayed on the surface of antigen-presenting cells in peripheral lymphoid organs. Whereas B cells recognize intact antigen, T cells recognize fragments of protein antigens that have been partly degraded inside the antigen- presenting cell. The peptide fragments are then carried to the surface of the presenting cell on special molecules called MHC proteins; ● The second difference is that, once activated, effector T cells act only at short range, either within a secondary lymphoid organ or after they have migrated into a site of infection. They interact directly with another cell in the body, which they either kill or signal in some way. Activated B cells, by contrast, secrete antibodies that can act far away.

31 Two main classes of T cells ● Effector cytotoxic T cells directly kill cells that are infected with a virus or some other intracellular pathogen. ● Effector helper T cells, by contrast, help stimulate the responses of other cellsmainly macrophages, B cells, and cytotoxic T cells

32 T cell receptor heterodimer

33 Activation of a T cell

34 Cytotoxic T cells kill their target cells

35 Differentiation of naïve helper T cells into either TH1 or TH2 effector helper cells

36 Recognition by T cells of foreign peptides bound to MHC proteins

37 Class I and class II MHC proteins

38 Human MHC genes

39 A peptide bound in the groove of a class I MHC protein

40 A peptide bound in the groove of a class II MHC protein

41 The interaction of a T cell receptor with a viral peptide bound to a class I MHC protein

42 CD4 and CD8 co-receptors on the surface of T cells

43 An effector cytotoxic T cell recognizes some aspect of the surface of the host target cell

44 The processing of a viral protein for presentation to cytotoxic T cells

45 The processing of an extracellular protein antigen for presentation to a helper T cell

46 Positive and negative selection in the thymus

47 The two signals that activate a helper T cell

48 The signaling events initiated by the binding of peptide-MHC complexes to T cell receptors

49 The stimulation of T cells by IL-2 in culture

50 The activation of TH1 and TH2 cells

51 Signaling events activated by the binding of antigen to B cell receptors (signal I)

52 The influence of B cell co- receptors on the effectiveness of signal I

53 Comparison of the signals required to activate a helper T cell and a B cell


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