Regulation of T follicular helper cell formation and function by antigen presenting cells

被引:78
作者
Deenick, Elissa K. [1 ,2 ]
Ma, Cindy S. [1 ,2 ]
Brink, Robert [1 ,2 ]
Tangye, Stuart G. [1 ,2 ]
机构
[1] St Vincents Hosp, Garvan Inst Med Res, Program Immunol, Darlinghurst, NSW 2010, Australia
[2] Univ NSW, St Vincents Clin Sch, Kensington, NSW 2033, Australia
基金
英国医学研究理事会;
关键词
CXC CHEMOKINE RECEPTOR-5; DENDRITIC CELLS; B-CELLS; ACTIVATION MOLECULE; HUMORAL IMMUNITY; OX40; LIGAND; EXPRESSION; DIFFERENTIATION; SAP; GENERATION;
D O I
10.1016/j.coi.2010.10.007
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
CD4(+) T cells can differentiate into numerous subsets characterized by expression of a suite of cytokines and effector molecules that endow them with specialized functions. By mediating the differentiation of B cells into memory and plasma cells following exposure to T-dependent antigens (Ag), T follicular helper (T-FH) cells have emerged as the predominant subset of CD4(+) T cells responsible for regulating humoral immunity. The generation of T-FH cells from naive precursors typically involves sequential cognate interactions with distinct populations of Ag-presenting cells (APCs): dendritic cells within the T-cell zone of lymphoid tissues, and activated B cells at the border of the T-zone and follicle, and then within a germinal canter. Recent studies have illuminated the key roles of APCs in T-FH development, and have also re-defined the role of B cells in this process.
引用
收藏
页码:111 / 118
页数:8
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