共 64 条
Origins of CD4+ effector and central memory T cells
被引:291
作者:

Pepper, Marion
论文数: 0 引用数: 0
h-index: 0
机构: Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA

Jenkins, Marc K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA
机构:
[1] Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA
关键词:
ROR-GAMMA-T;
IN-VIVO;
TH17;
CELLS;
HELPER-CELLS;
DIFFERENTIATION;
GENERATION;
INFECTION;
RECEPTOR;
ANTIGEN;
ACTIVATION;
D O I:
10.1038/ni.2038
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Lineage-committed effector CD4(+) T cells are generated at the peak of the primary response and are followed by heterogeneous populations of central and effector memory cells. Here we review the evidence that T helper type 1 (T(H)1) effector cells survive the contraction phase of the primary response and become effector memory cells. We discuss the applicability of this idea to the T(H)2 cell, T(H)17 helper T cell, follicular helper T cell (T-FH cell) and induced regulatory T cell lineages. We also discuss how central memory cells are formed, with an emphasis on the role of B cells in this process.
引用
收藏
页码:467 / 471
页数:5
相关论文
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