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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