Complementary contribution of CD4 and CD8 T lymphocytes to T-cell infiltration of the intact and the degenerative spinal cord

被引:36
作者
Bradl, M
Bauer, J
Flügel, A
Wekerle, H
Lassmann, H
机构
[1] Brain Res Inst, Dept Neuroimmunol, Vienna, Austria
[2] Max Planck Inst Neurobiol, Dept Neuroimmunol, Martinsried, Germany
基金
奥地利科学基金会;
关键词
D O I
10.1016/S0002-9440(10)62361-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The central role of T cells in inflammatory reactions of the central nervous system (CNS) is well documented. However, there is little information about the few T cells found within the noninflamed CNS. In particular, the contribution of CD4(+) and CD8(+) T cells to the lymphocyte pool infiltrating the intact CNS, the location of these cells in CNS white and gray matter, and changes in the cellular composition of T-cell infiltrates coinciding with degeneration are primarily undefined. To address these points, we studied T cells in the intact and degenerative rat spinal cord. in the intact spinal cord, T cells were preferentially located within the gray matter. CD8(+) T cells were more numerous than CD4(+) lymphocytes. In cases of neuroaxonal degeneration or myelin degeneratioa/oligodendrocyte death, T cells were predominantly seen in areas of degeneration and were present in increased numbers. These effects were more pronounced for the CD4(+) than for the CD8(+) T-cell subset. Collectively, these data provide evidence for a clear cellular and compartmental bias in T-cell infiltration of the intact and degenerative spinal cord. This could indicate that CD4(+) and CD8(+) T cells might fulfill complementary roles in the intact and the diseased organ.
引用
收藏
页码:1441 / 1450
页数:10
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