A revised view of the central nervous system microenvironment and major histocompatibility complex class II antigen presentation

被引:5
|
作者
Perry, VH [1 ]
机构
[1] Univ Oxford, Dept Pharmacol, CNS Inflammat Grp, Oxford OX1 3QT, England
基金
英国惠康基金;
关键词
central nervous system; MHC class II; T-cell;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There are numerous observations reporting that phagocytes expressing major histocompatibility complex (MHC) Class II molecules are associated with the central nervous system (CNS) in normal and pathological conditions. Although MHC Class II: expression is necessary for antigen presentation to CD4 + T-cells, it is not sufficient and co-stimulatory molecules are also required. We review here recent in vivo studies demonstrating that the microglia and perivascular macrophages are unable to initiate a primary immune response in the CNS microenvironment, but may support secondary immune responses. Although in vitro studies show that microglia do not support a primary immune response leading to T-cell, proliferation, they do show that microglia may protect the CNS from the unwanted attentions of autoreactive T-cells by inducing their apoptosis. The lack of cells in the CNS parenchyma with the ability to initiate a primary immune response has a cost, namely that pathogens may persist in the CNS undetected by the immune system. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:113 / 121
页数:9
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