An antigen-specific pathway for CD8 T cells across the blood-brain barrier

被引:172
作者
Galea, Ian [1 ]
Bernardes-Silva, Martine
Forse, Penny A.
van Rooijen, Nico
Liblau, Roland S.
Perry, V. Hugh
机构
[1] Univ Southampton, Sch Biol Sci, CNS Inflammat Grp, Southampton SO16 7PX, Hants, England
[2] Dept Mol Cell Biol, NL-1007 MB Amsterdam, Netherlands
[3] Purpan Hosp, Ctr Physiopathol Toulouse Purpan, Inst Natl Sante & Rech Med U563, F-31000 Toulouse, France
基金
英国惠康基金;
关键词
D O I
10.1084/jem.20070064
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8 T cells are nature's foremost defense in encephalitis and brain tumors. Antigen-specific CD8 T cells need to enter the brain to exert their beneficial effects. On the other hand, traffic of CD8 T cells specific for neural antigen may trigger autoimmune diseases like multiple sclerosis. T cell traffic into the central nervous system is thought to occur when activated T cells cross the blood-brain barrier ( BBB) regardless of their antigen specificity, but studies have focused on CD4 T cells. Here, we show that selective traffic of antigen-specific CD8 T cells into the brain occurs in vivo and is dependent on luminal expression of major histocompatibility complex ( MHC) class I by cerebral endothelium. After intracerebral antigen injection, using a minimally invasive technique, transgenic CD8 T cells only infiltrated the brain when and where their cognate antigen was present. This was independent of antigen presentation by perivascular macrophages. Marked reduction of antigen-specific CD8 T cell infiltration was observed after intravenous injection of blocking anti-MHC class I antibody. These results expose a hitherto unappreciated route by which CD8 T cells home onto their cognate antigen behind the BBB: luminal MHC class I antigen presentation by cerebral endothelium to circulating CD8 T cells. This has implications for a variety of diseases in which antigen-specific CD8 T cell traffic into the brain is a beneficial or deleterious feature.
引用
收藏
页码:2023 / 2030
页数:8
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