Not all effector CD8+ T cells are alike

被引:2
|
作者
Drake, DR
Braciale, TJ
机构
[1] Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USA
[2] Univ Virginia, Dept Pathol, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
关键词
effector CD8(+) T cells; MHC;
D O I
10.1016/S1286-4579(03)00011-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As naive CD8(+) T cells circulate throughout the bloodstream and secondary lymphoid tissues (i.e. spleen and lymph nodes), they sample complexes of peptides and MHC class I molecules expressed on the surface of professional antigen presenting cells (APCs). A proper fit between lymphocyte and APCs sets into motion a complex series of events that result in the generation of activated cytotoxic T lymphocytes (CTLs) that are the principal immune effectors against infected and transformed cells. Owing to the severe immunopathology that can result from the aberrant stimulation of CTLs, the activation of naive CD8(+) T cells is a tightly regulated process. A growing body of evidence suggests that the quality of stimulation naive CD8(+) T cells receive during the induction and maintenance of an immune response dictates the functional competency of the responding antigen- specific CTLs, and that CD8(+) T cells and their progeny "effector cells" can exist long-term in vastly different activation states. (C) 2003 Editions scientifiques er medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:199 / 204
页数:6
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