In the last two decades, it has become clear that yo T cells recognize a diverse array of antigens including self and foreign, large and small, and peptidic and non-peptidic molecules. In this respect, 78 antigens as ...In the last two decades, it has become clear that yo T cells recognize a diverse array of antigens including self and foreign, large and small, and peptidic and non-peptidic molecules. In this respect, 78 antigens as a whole resemble more the antigens recognized by antibodies than those recognized by T cells. Because of this antigenic diversity, no single mechanism--such as the major histocompatibility complex （MHC） restriction of ap T cells--is likely to provide a basis for all observed T-cell antigen receptor （TCR）-dependent 78 T-cell responses. Furthermore, available evidence suggests that many individual 78 T cells are poly-specific, probably using different modes of ligand recognition in their responses to unrelated antigens. While posing a unique challenge in the maintenance of self-tolerance, this broad reactivity pattern might enable multiple overlapping uses of 78 T-cell populations, and thus generate a more efficient immune response.展开更多
文摘In the last two decades, it has become clear that yo T cells recognize a diverse array of antigens including self and foreign, large and small, and peptidic and non-peptidic molecules. In this respect, 78 antigens as a whole resemble more the antigens recognized by antibodies than those recognized by T cells. Because of this antigenic diversity, no single mechanism--such as the major histocompatibility complex （MHC） restriction of ap T cells--is likely to provide a basis for all observed T-cell antigen receptor （TCR）-dependent 78 T-cell responses. Furthermore, available evidence suggests that many individual 78 T cells are poly-specific, probably using different modes of ligand recognition in their responses to unrelated antigens. While posing a unique challenge in the maintenance of self-tolerance, this broad reactivity pattern might enable multiple overlapping uses of 78 T-cell populations, and thus generate a more efficient immune response.
