FUNCTIONAL CD4 T-CELL SUBSET INTERPLAY IN AN INTACT IMMUNE-SYSTEM

被引:0
|
作者
MURRAY, JS
MADRI, J
PASQUALINI, T
BOTTOMLY, K
机构
[1] YALE UNIV,SCH MED,HOWARD HUGHES MED INST,IMMUNOBIOL SECT,310 CEDAR ST,NEW HAVEN,CT 06510
[2] YALE UNIV,SCH MED,DEPT PATHOL,NEW HAVEN,CT 06510
来源
JOURNAL OF IMMUNOLOGY | 1993年 / 150卷 / 10期
关键词
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
Immunization with human collagen IV has been shown to lead to the selective activation of Th-1 and Th-2-like cells in vivo depending on the I-A genotype of the mice. Mice expressing I-A(s) generate Th-1 cells, and mice expressing I-A(b) generate Th-2 cells after immunization. We examined the response of (bxs)F1 hybrid mice to determine the types of CD4 T cell activated. We found that Th-1-like responses dominated, in that CD4 T cells from human collagen IV-primed mice displayed good proliferative responses and little ability to induce antibody formation, and secreted IFN-gamma and not IL-5. Most of the Th-1 -like activity of F1 hybrid T cells was I-A(s) restricted. inhibition of Th-1 cell priming using anti-I-A(s) antibody administered with the priming Ag in vivo revealed Th-2-like activity, in that the CD4 T cells now secreted IL-5 and not IFN-gamma and induced antibody formation. Additional studies indicated that anti-IFN-gamma treatment in vivo also revealed Th-2 cells, suggesting that I-A(s)-restricted CD4 T cells producing or controlling the production of IFN-gamma suppress Th-2 priming.
引用
收藏
页码:4270 / 4276
页数:7
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