Malaria Programme, MRC Laboratories, Fajara, PO Box 273 Banjul, The Gambia.
Trends Immunol. 2010 Feb;31(2):63-70. doi: 10.1016/j.it.2009.12.002. Epub 2010 Jan 6.
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.
T 细胞介导的炎症免疫反应既有助于清除疟疾感染,也与感染后的病理变化有关;一旦寄生虫血症得到控制,宿主下调炎症的能力对于避免免疫介导的病理变化至关重要,但目前对此仍知之甚少。各种调节性 T 淋巴细胞群体可以调节炎症免疫反应,最近人们对调节性 T 细胞是否可能改变实验动物和人类疟疾感染的结果产生了浓厚的兴趣。在这里,我们回顾了这些研究,特别关注了最近在人类中的研究,提出了一个模型,说明不同的调节性 T 细胞群体可能在感染的不同阶段对炎症的控制做出贡献,并讨论了这对设计安全有效的疟疾疫苗的影响。