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Immunological Synapse (Paperback, 2010 ed.)
Loot Price: R4,221
Discovery Miles 42 210
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Immunological Synapse (Paperback, 2010 ed.)
Series: Current Topics in Microbiology and Immunology, 340
Expected to ship within 10 - 15 working days
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The proper physiological functioning of most eukaryotic cells
requires their assembly into multi-cellular tissues that form
organized organ systems. Cells of the immune system develop in bone
marrow and lymphoid organs, but as the cells mature they leave
these organs and circulate as single cells. Antigen receptors
(TCRs) of T cells search for membrane MHC proteins that are bound
to peptides derived from infectious pathogens or cellular
transformations. The detection of such speci?c peptide-MHC antigens
initiates T cell activation, adhesion, and immune-effectors
functions. Studies of normal and transformed T cell lines and of T
cells from transgenic mice led to comprehensive understanding of
the mole- lar basis of antigen-receptor recognition and signaling.
In spite of these remarkable genetic and biochemical advances,
other key physiological mechanisms that par- cipate in sensing and
decoding the immune context to induce the appropriate cellular
immune responses remain unresolved. TCR recognition is tightly
regulated to trigger sensitive but balanced T cell responses that
result in the effective elimination of the pathogens while
minimizing collateral damage to the host. The sensitivity of TCR
recognition has to be properly tempered to prevent unintended
activation by self-peptide-MHC complexes that cause autoimmune
diseases. It is likely that once the TCR is engaged by a peptide-
MHC and TCR signaling begins, additional regulatory mechanisms,
involving other receptors, would increase the ?delity of the
response.
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