Heterogeneity of CD4+ memory T cells: Functional modules for tailored immunity

被引:277
作者
Sallusto, Federica [1 ]
Lanzavecchia, Antonio [1 ]
机构
[1] Inst Biomed Res, CH-6500 Bellinzona, Switzerland
基金
瑞士国家科学基金会;
关键词
CD4(+) T cells; Memory cells; T-cell subsets; GROWTH-FACTOR-BETA; ROR-GAMMA-T; CYTOKINE GENE-EXPRESSION; CXC CHEMOKINE RECEPTOR-5; FOLLICULAR-HELPER-CELLS; HYPER-IGE SYNDROME; TGF-BETA; TRANSCRIPTION FACTOR; NONLYMPHOID TISSUE; T-H-17; CELLS;
D O I
10.1002/eji.200939722
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Phenotypic and functional heterogeneity is the hallmark of effector and memory T cells. Upon antigenic stimulation, naive CD4(+) T cells make choices to become effector Th1, Th2 or Th17 cells, or even Treg. In addition to differences in cytokine repertoire, effector CD4(+) T cells exhibit diversity in homing, such as migration to lymph node follicles to help B cells versus migration to inflamed tissues. Upon clearance of the antigen, two major types of memory T cells remain: central memory cells, which patrol lymphoid organs, and effector memory cells that act as sentinels in peripheral tissues such as the skin and the gut. Here, we review our current understanding of CD4(+) T-cell lineage heterogeneity and flexibility, with emphasis on the human system, and propose an organization of effector and memory T cells based on distinct functional modules.
引用
收藏
页码:2076 / 2082
页数:7
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