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Published byGarry Merritt Modified over 9 years ago
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ADAPTIVE IMMUNITY
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Adaptive immunity Specific Slow during the primary response, but very fast during the secondary responses memory
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Specificity is achieved by BCRs and TCRs Each B cell express a unique BCR and each T cell express a unique TCR Clonal selection!
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B cell receptor (BCR)
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HUMORAL RESPONSE Circulating B cells which have not been exposed to the antigen naive B cells When BCR binds to the antigen, the antigen is internalised by the B cell and presented to the T cells
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Activated t cells induce -Cell surface proteins (CD40L) -Cytokines -Activated B cell divide rapidly and differntiate to plasma cell -This events take in germinal centres of lymphnodes and spleen
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The first IG is always IgM Later different cytokines instruct B cells to secrete different IG classes (isotype switching)
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IG diversity Differnt gene segments on different chromosomes encode heavy and light chains These multigene families are separated by non-coding regions and are brought together with gene rearrengements.
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Light chain V about 76 J 5 C 1 Heavy chains V 123-129 D 27 J 9 C 11 Recombinase activating gene RAG-1 and RAG 2 recombinase responsible for the VDJ recombination
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Isotype switching: IL-4 IgG and IgE IL-5 IgA DNA sequences known as “switch sites” are located upstream of heavy constant region on the DNA (M, D, G, E and A) IgM and IgD do not have switch sites Affinity maturatin Somatic hypermutation (random mutationx in V regions)
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Cell mediated immunity CMI is the major component of immune response T cell are essential cells influencing Cytokine production, B cell activation, macrophage activation, rejection, killling of tumor or infected cells, DTH
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TCR Gamma-delta TCR bearing cells are found in skin, epitelial and intestinal layers Antigen recognition is MHC restricted Alfa-gamma V, D and J; Beta, delta V and J rearrengements No somotic hypermutation
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TH17 CD4+ cells producing IL-17 and 22 Early immune response to bacteria Autoimmunity Immunity against fungi
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Treg CD4+CD25 + FOXP3
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