Pathophysiology of T follicular helper cells in humans and mice

被引:344
作者
Ueno, Hideki [1 ]
Banchereau, Jacques [2 ,3 ]
Vinuesa, Carola G. [4 ]
机构
[1] Baylor Inst Immunol Res, Dallas, TX 75204 USA
[2] Jackson Lab Genom Med, Farmington, CT USA
[3] Hop Henri Mondor, INSERM, U955, Vaccine Res Inst, F-94010 Creteil, France
[4] Australian Natl Univ, John Curtin Sch Med Res, Dept Pathogens & Immun, Canberra, ACT 2601, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; CENTER B-CELL; SIMIAN IMMUNODEFICIENCY VIRUS; CHRONIC LYMPHOCYTIC-LEUKEMIA; GERMINAL CENTER FORMATION; PROTEIN-COUPLED RECEPTOR; CXC CHEMOKINE RECEPTOR-5; NONOBESE DIABETIC MICE; MEMORY TFH CELLS; ANTIBODY-RESPONSES;
D O I
10.1038/ni.3054
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Follicular helper T cells (T-FH cells) compose a heterogeneous subset of CD4(+) T cells that induce the differentiation of B cells into plasma cells and memory cells. They are found within and in proximity to germinal centers in secondary lymphoid organs, and their memory compartment also circulates in the blood. Our knowledge on the biology of T-FH cells has increased significantly during the past decade, largely as a result of mouse studies. However, recent studies on human T-FH cells isolated from lymphoid organ and blood samples and recent observations on the developmental mechanism of human T-FH cells have revealed both similarities and differences between human and mouse T-FH cells. Here we present the similarities and differences between mouse and human lymphoid organ-resident T-FH cells and discuss the role of T-FH cells in response to vaccines and in disease pathogenesis.
引用
收藏
页码:142 / 152
页数:11
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