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NEGATIVE REGULATION OF THE IMMUNE SYSTEM

NEGATIVE REGULATION OF THE IMMUNE SYSTEM. NEGATIVE REGULATION IN THE IMMUNE SYSTEM Decrease of antigen concentration in the course of the immune response Inhibition of B lymphocyte activation - antibody feedback Cross linking of BCR with Fc  RIIB (CD32) by antigen-antibody complex

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NEGATIVE REGULATION OF THE IMMUNE SYSTEM

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  1. NEGATIVE REGULATION OF THE IMMUNE SYSTEM

  2. NEGATIVE REGULATION IN THE IMMUNE SYSTEM • Decrease of antigen concentration in the course of the immune response • Inhibition of B lymphocyte activation - antibody feedback • Cross linking of BCR with FcRIIB (CD32) by antigen-antibody complex • ITIM-induced negative signaling of B cell activation - phosphatases • B cells without T cell help are excluded from follicles • Death of activated T lymphocytes • Passive cell death mediated by the shortage in survival factors (cytokines) • Activation induced FasL expression sensitizes activated T cells for Fas- • mediated apoptosis (AICD) • Activation induced cell death (AICD) is induced by repeated antigenic stimulation • 4. Inhibition T lymphocyte activation • Anergy of CD4+ T lymphocytes • Late in the immune response activated T cells express CTLA-4, the ligand of B7 • Suppression by regulatory T lymphocytes • Counter regulation of Th1 and Th2 cytokines • Production of suppressive cytokines • IL-10 inhibits APC function such as IL-12 secretion and B7 expression • TGF inhibits T-cell proliferation • IL-4 inhibits IFN-mediated functions • IL-10 and TGF inhibit macrophage activation

  3. NEGATIVE REGULATION OF IMMUNE RESPONSES AICD DIFFERENTIATION Naive lymphocytes Memory Primary effectors Secondary effectors Number of antigen specific cells EXPANSION AICD MEMORY

  4. IMMUNOGLOBULIN BINDING Fc RECEPTORS FcγRI (CD64) FcγRII (CD32) FcεRI FcεRII Iγ-γ αβγ-γαγ-γ FcγRIII (CD16) FcRI IIIaζ-ζ IIIaζ-γ IIIaγ-γ IIIaβ γ-γα IgG Fc receptors Ig supergene family, MIRR

  5. ACTIVATING AND INHIBITORY RECEPTORS IN THE IMMUNE SYSTEM • MIRRMultisubunit Immune Recognition Receptors • The ligand binding and signal transducing subunits are separated, they co-localize in membrane microdomains.

  6. ITAM ITIM NEGATIVE REGULATION OF B LYMPHOCYTES BY IMMUNE COMPLEXES FcRIIb

  7. Costimulatory molecules also associate with inhibitory receptors T cell Activated T cell - - - - - 2 2 Signal 1 + /CTLA-4 CD28 CD28 B7 B7 Cross-linking of CTLA-4 by B7 inhibits co-stimulation and inhibits T cell activation CD28 cross linked by B7 Co-stimulation induces CTLA-4 CTLA-4 binds CD28 with a higher affinity than B7 molecules The lack of signal 2 to the T cell shuts down the T cell response.

  8. NEGATIVE REGULATION OF T CELL ACTIVATION BY CTLA-4 T APC CD28 B7 CTLA-4 LATE EXPRESSION HIGHER AFFINITY TO B7 THAN CD28

  9. THE ROLE OF CD4+ T CELLS IN APOPTOSIS T CELL HOMEOSTASIS SHUT OFF IMMUNE RESPONSES

  10. REGULATORY T CELLS

  11. REGULATORY T CELLS FoxP3 MARKERS OF THYMUS DERIVED NATURAL Treg CELLS CD4+CD25+FOXP3+ GITR CTLA4 B7 ligand Treg CD25 IL-2Rα CD127 IL-7Rα↓ Treg differentiation, maintenance, function Transcription factor – many target genes Itself is not sufficient to confer suppressive function A TGFβ does not induce regulatory function

  12. FUNCTIONS OF REGULATORY T CELLS • Maintenance of peripheral tolerance • Prevention of autoimmunity • Limiting inflammatory processes (asthma, inflammatory bowel diseases) • Inhibit protection against infectious diseases • Limit immune responses to tumors MECHANISM Intrinsic and extrinsic regulation Various inhibitory mechanisms Cell contacts – Cytokines Interaction with the target effector T cells

  13. REGULATORY FUNCTION OF REGULATORY T LYMPHOCYTES IL-35 TGFβ IL-10 Inhibitory cytokines Cytolysis Metabolic dysregulation Inhibition of dendritic cell maturation Indolamin2,3-dioxigenase LAG-3 – CD4 homolog Treg : effektor T cell = 1 : 8 Treg : DC = 1 : 0,8 Descreased cytokine production (IL-2) Adenosin around the cell cAMP transfer

  14. THE ROLE OF IL-35 IN THE FUNCTION OF REGULATORY T CELLS Initial T cell activation Sensed by Treg cells Increased suppressive mechanisms • The molecular patterns of activated Treg cells are different in the presence and absence of effector cells • The expression of EBI3 and IL-12α/p35 (IL-35) subunits is increased in the presence of effector T cells • Treg cells in contact with effector cell act also on effector cells out of contact through IL-35 Induced capability, the effector cell is involved NOT ONLY A FUNCTION

  15. REGULATORY CELLS ARE ABLE TO CONTROL LOW LEVEL ACTIVATION

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