Regulatory T cells in malaria - friend or foe?

被引:68
作者
Finney, Olivia C. [1 ,2 ]
Riley, Eleanor M. [2 ]
Walther, Michael [1 ]
机构
[1] MRC Labs, Malaria Programme, Banjul, Gambia
[2] Univ London London Sch Hyg & Trop Med, Immunol Unit, Dept Infect & Trop Med, London WC1E 7HT, England
关键词
GROWTH-FACTOR-BETA; PLASMODIUM-YOELII; TGF-BETA; CHILDHOOD MALARIA; CLINICAL IMMUNITY; FALCIPARUM; INFECTION; RESPONSES; PARASITE; SUSCEPTIBILITY;
D O I
10.1016/j.it.2009.12.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell-mediated inflammatory immune responses contribute to both the clearance and pathology of malaria infections; the host's ability to down-regulate inflammation once parasitemia is controlled is crucial to avoid immune-mediated pathology but remains poorly understood. Various regulatory populations of T lymphocytes can modulate inflammatory immune responses and there has been considerable recent interest in the potential for regulatory T cells to modify the outcome of both murine and human malaria infections. Here, we review these studies, focussing in particular on recent studies in humans, propose a model by which different regulatory T cell populations might contribute to the control of inflammation at different stages of infection and discuss the implications for the design of safe and effective malaria vaccines.
引用
收藏
页码:63 / 70
页数:8
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