Th2 immune regulation induced by T cell vaccination in patients with multiple sclerosis

被引:3
|
作者
Zang, YCQ
Hong, J
Tejada-Simon, MV
Li, SF
Rivera, VM
Killian, JM
Zhang, JWZ
机构
[1] Baylor Coll Med, Dept Neurol, Multiple Sclerosis Res Lab, Houston, TX 77030 USA
[2] Baylor Methodist Multiple Sclerosis Ctr, Houston, TX USA
[3] Baylor Coll Med, Dept Immunol, Houston, TX 77030 USA
[4] Vet Adm Med Ctr, Neurol Serv, Houston, TX 77211 USA
关键词
autoimmunity; autoreactive T cell; cytokine; multiple sclerosis; myelin basic protein;
D O I
10.1002/1521-4141(200003)30:3<908::AID-IMMU908>3.0.CO;2-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell responses to myelin basic protein (MBP) are potentially involved in the pathogenesis of multiple sclerosis (MS). In this study, we demonstrated that subcutaneous inoculations with irradiated autologous MBP-reactive T cell clones (T cell vaccination) elicited CD8(+) antiidiotypic T cell responses and CD4(+) Th2 cell responses in patients with MS. Both regulatory cell types induced by T cell vaccination contributed to the inhibition of MBP-reactive T cells while they differed in the recognition pattern and functional properties. We describe for the first time that the Th2 regulatory cells reacted with activated but not resting T cells in the context of MHC class II molecules and inhibited the proliferation of MBP-reactive T cells through the secretion of IL-4 and IL-10. The T-T cell interaction mediated by Th2 regulatory cells was independent of the antigen specificity of activated T cells. The findings have important implications for our understanding of the regulatory mechanism induced by T cell vaccination.
引用
收藏
页码:908 / 913
页数:6
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