AN ENDOGENOUS RETROVIRUS MEDIATING DELETION OF ALPHA-BETA T-CELLS

被引:313
作者
WOODLAND, DL
HAPP, MP
GOLLOB, KJ
PALMER, E
机构
[1] NATL JEWISH CTR IMMUNOL & RESP MED, DEPT PEDIAT, DIV BASIC SCI, DENVER, CO 80206 USA
[2] UNIV COLORADO, HLTH SCI CTR, DEPT MICROBIOL & IMMUNOL, DENVER, CO 80262 USA
关键词
D O I
10.1038/349529a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A SPECIAL class of self-antigens (endogenous superantigens) is capable of deleting many murine T cells on the basis of their expression of particular T-cell receptor V-beta gene segments. In mice that endogenously express these antigens, tolerance is mediated in part by the clonal deletion of the relevant V-beta-bearing T cells 1-17. The deletion of I-E-reactive V-beta-5.2-bearing T cells is dependent on the coexpression of an I-E tolerogenic coligand (Etc) 14 and the gene for one of these coligands, Etc-1, maps to chromosome 12, near the mouse mammary tumour viral integrant, Mtv-9. Here we report a perfect genetic linkage between Etc-1 and Mtv-9 and show that Etc-1 is also involved in the I-E-dependent deletion of T cells bearing V-beta-5.1 and V-beta-11 domains. We also demonstrate that Mtv-9 transcripts are present in B cells expressing Etc-1 and suggest that the coligand recognized by roughly 15% of all T lymphocytes is encoded by the Mtv-9 genome.
引用
收藏
页码:529 / 530
页数:2
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