Early activation of microglia as antigen-presenting cells correlates with T cell-mediated protection and repair of the injured central nervous system

被引:110
作者
Shaked, I
Porat, Z
Gersner, R
Kipnis, J
Schwartz, M [1 ]
机构
[1] Weizmann Inst Sci, Dept Neurobiol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Biol Regulat, IL-76100 Rehovot, Israel
关键词
protective autoimmunity; encephalitogenicity; neuroprotection; CNS inflammation; CNS trauma; genetic background; EAE susceptibility; microglia activation;
D O I
10.1016/j.jneuroim.2003.10.049
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After an injury to the central nervous system (CNS), activated microglia have been shown to contribute to the ongoing destructive processes leading to secondary neuronal degeneration. They can, however, also express neuroprotective activity. Studies from our laboratory point to the existence of a physiological T cell-mediated neuroprotective mechanism (adaptive immunity) that is amenable to boosting. We postulate that the beneficial or destructive outcome of the local microglial (innate) response is determined by a well-controlled dialog between the innate and the adaptive immune players. Here, we show that spontaneous or exogenously boosted cell-mediated neuroprotection is correlated with early activation of microglia as antigen-presenting cells. We suggest that such microglial activity, if well controlled, is a crucial step in determining the fate of the neurons in a hostile environment. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 93
页数:10
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