Effector CD4+ T cells, the cytokines they generate, and GVHD: something old and something new

被引:140
作者
Coghill, James M. [1 ,2 ]
Sarantopoulos, Stefanie [1 ,2 ,3 ]
Moran, Timothy P. [4 ]
Murphy, William J. [5 ]
Blazar, Bruce R. [6 ]
Serody, Jonathan S. [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Pediat, Chapel Hill, NC 27599 USA
[5] Univ Calif Davis, Dept Dermatol, Davis, CA 95616 USA
[6] Univ Minnesota, Med Ctr, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; GROWTH-FACTOR-BETA; MINOR HISTOCOMPATIBILITY ANTIGEN; CXC CHEMOKINE RECEPTOR-5; FOLLICULAR HELPER-CELLS; NECROSIS-FACTOR-ALPHA; HUMAN T-H-17 CELLS; ROR-GAMMA-T; TGF-BETA;
D O I
10.1182/blood-2010-12-290403
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GVHD is a syndrome that results from minor and major histocompatibility complex incompatibilities between the donor and recipient. More than 50 years after its initial description, the pathophysiology of GVHD remains poorly understood. Nonetheless, donor T cells have been shown to be critical to the pathophysiology of acute and chronic GVHD, yet precisely how they function remains unclear. The effector mechanisms by which donor T cells mediate tissue inflammation is even less well understood. Identification of several new lineages of CD4(+) T cells made in the past decade and their roles in the pathophysiology of T cell-mediated diseases has shed new light on these effector mechanisms. In this review, we summarize the recent descriptions of these T-cell lineages and the current data supporting their role in acute and to a lesser extent chronic GVHD. Investigations into the activity of these new T-cell lineages may provide more rationale approaches to the treatment or prevention of GVHD. (Blood. 2011;117(12):3268-3276)
引用
收藏
页码:3268 / 3276
页数:9
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