a reasonable if fairly narrow essay (narrow in subject that is) cant remember How does the body achieve the functional silencing of antigen responsive clones? The central doctrine of the immune system is the ability to be intimate and remove non-self components without touch on self components. The T cellphones and B cells of the immune system secern a vast repertoire of antigen receptors. It is thought that the germline TCR repertoire is imperturbable of in the region of at least 109 different specificities. Considering the probable number of antigens that may be bound by these receptors it is unavoidable that a dimension of them leave be tar totaled against self components. Tolerance in the T cell repertoire. Central gross profit. three T cell mechanisms for self tolerance: clonal deletion, clonal anergy and antigen specific suppressor T cells. Burnet proposed realizable action of clonal deletion in 1955. Marrack (1987) showed that T cells objective receptors containing a member of the Vb17 family were absent from mice expressing the MHC mannikin-II molecule I-E, with which the Vb17 chain is reactive. elevate support has been provided by the absence of self-reactive clones in mice expressing a superantigen such(prenominal) as kid lymphocyte stimulating antigen - an antigen which binds to the TCR in a manner that is self-reliant of the Va chain and thus binds a more larger proportion of T cells than conventional antigens. in the thymus gland self reactive TCR place at the CD4+8+ branch, non at the CD4+8- or CD4-8+ stage à deletion occurred during thymocyte development. There is evidence that deletion occurs while thymocytes atomic number 18 in their double unconditional state - CD8+ thymocytes bearing receptors specific for class II MHC molecules are deleted during thymocyte development - surprising since CD8+cells are normally MHC I curtail If deletion was mediated via an interaction between TCR/CD8 and MHC/peptide... If you indi! spensableness to get a full essay, order it on our website: OrderCustomPaper.com
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