immune resp & immunomechimmunomechanism

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     A. Positive selection: If the thymocyte TCR engages in a low-affinity interaction with a self MHC molecules on athymic epithelial cell it is rescue! from programme! cell !eath an! continues to mature

    ". #ac$ of positive selection: If the thymocyte TCR !oes not engage in any interaction with pepti!e-MHCmolecule comple%es on thymic epithelial cell it will !ie in a programme! cell !eath

    C. &egative selection: If the thymocyte TCR binds pepti!e-MHC comple%es on a thymic antigen presentingcell with high avinity it is in!uce! to un!ergo apoptotic cell !eath

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    Immune Response '

    Immunomechanism

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    The line of !efence against micro(es

    )Protective surface mechanism* +pithelia:

    ) ,$in: impenetra(le (arrier) Resp tract: surface mucous ciliary action) Maintenance of aci!ic environment stomach vagina

    *  Antimicro(ial su(stances pro!uce! at epithelial surface

    ) &on-specific tissue !efences

    * Phagocytic cells an! &atural /iller cells) Macrophages) &eutrophils) &/ cells

    * "loo! Proteins) Mem(er of complement system) Me!iators of inflammation

    * Inflammation* &eutrophil recruitment

    * Cyto$ines) Proteins that regulate an! coor!inate many of the activities of the cells of innate

    immunity 

    ) ,pecific immune responses*  A!aptive immune response

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    Physical and chemical barriers

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     A&TI1+& R+C21&ITI2&

    ) Innate immunity  )  A!aptive immunity 

    Pathogen-associate!molecular patternPAMPs recogni0e! (yT#R e%presse! inphagocytic cells

    T cells ReceptorsC345 helper T cell

    TCRrecogni0e!antigen

    pepti!e inassociation with class II MHCmolecule

    C365 cytoto%ic Tcellrecogni0e!pepti!eantigen inassociation with class I MHCmolecules

    B cell

    Recognized peptide antigenthroughsurface immuno lobulin

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    ,pecific immune responseInitiation

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    C34Tcell activation an! 3ifferentiation

    ) Naïve CD4 T cell activated bydendritic cell

    )  ctivated CD4 T cell differentiate intoeffector CD4 T cells! T"#$ T"%$ T"#&$TReg

    ) Differentiation is initiated through an

    interaction of DC and CD4' " T cells 

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    TH7 cells coor!inate the host

    response to intracellular pathogens

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    Professional antigen-presenting cells

    (APCs) are distributed in dierentregions of the lymph nodes: 

    • Dendritic cells are found throughout thecortexin the T-cell areas

    • Macrophages are found throughout thecortex

    and the follicles• B cells are found mainly in the follicles

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    Activation of naïve T cells requires twoindependent signals:! T"#$co-receptor %indingof M&"$peptide complextransmits the 'rst signal(arro) *!+! Activation of the T cellrequires a second signal(arro) +* to %e delivered%y the same antigen-

    presenting cell! 

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    The principal co-stimulatory

    molecules expressed on

    professional antigen-presentingcells are B7 molecules, which

    bind the T-cell protein, CD28. 

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    Bacterial ,. induces ,angerhans cellsto migrate to lymphonodus/ matureand initiating adaptive immunity

    Activation of "D0 T cells required costimulatory molecules/ "D12 (B3!*4 "D15(B3!+*Activation of B cells required the help ofactivated "D0 T cells

    ,ymphocyte activation occur in T-celldependent 6one of lymphonodus

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    Immune tolerance

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    In!uction of Tolerance

    )  Antigen segregation

    * Immuneprivile!ge site

    ) In!uction of tolerance

    * Central tolerance) 3eletion of autoreactive lymphocytes !uring !evelopment

    * Peripheral tolerance) 3eletion of autoreactive lymphocytes (y 

    * Apoptosis clonal !eletion* Anergy functionally in activate!

    * ,upression (y a Regulatory T cells

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    H2M+2,TA,I,

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     Autoimmune !iseases

    The normal immune system must (e a(le to!istinguish (etween self an! non-self 

     Autoimmune !isease is a (rea$!own oftolerance

     Autoimmune !isease is a hypersensitivityreaction triggere! (y self antigens

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