TL ANTIGEN AS A TRANSPLANTATION ANTIGEN RECOGNIZED BY TL-RESTRICTED CYTOTOXIC T-CELLS

被引:34
作者
MORITA, A
TAKAHASHI, T
STOCKERT, E
NAKAYAMA, E
TSUJI, T
MATSUDAIRA, Y
OLD, LJ
OBATA, Y
机构
[1] AICHI CANC CTR,RES INST,IMMUNOL LAB,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN
[2] NAGOYA CITY UNIV,SCH MED,DEPT DERMATOL,MIZUHO KU,NAGOYA,AICHI 467,JAPAN
[3] OKAYAMA UNIV,SCH MED,DEPT PARASITOL & IMMUNOL,OKAYAMA,OKAYAMA 700,JAPAN
[4] MEM SLOAN KETTERING CANC CTR,LUDWIG INST CANC RES,NEW YORK UNIT,NEW YORK,NY 10021
关键词
D O I
10.1084/jem.179.3.777
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In contrast to broadly expressed classical class I antigens of the major histocompatibility complex, structurally closely related TL antigens are expressed in a highly restricted fashion. Unlike classical class I antigens, TL antigens are not known to be targets of cytotoxic T cells or to mediate graft rejection. Whereas classical class I antigens function as antigen-presenting molecules to T cell receptors (TCR), the role of TL is yet to be defined. To elucidate the function of TL, we have derived transgenic mice expressing TL in most tissues including skin by introducing a TL gene, T3(b) of C57BL/6 mouse origin, driven by the H-2K(b) promoter. By grafting the skin of transgenic mice, we demonstrate that TL can serve as a transplantation antigen and mediate a TCR-alpha/beta(+) CD8(+) cytotoxic T cell response. This T cell recognition of TL does not require antigen presentation by H-2 molecules. Furthermore, we show that C57BL/6 F-1 mice develop CD8(+) T cells that are cytotoxic for C57BL/6 TL(+) leukemia cells, providing further support for the concept that aberrantly expressed nonmutated proteins such as TL can be recognized as tumor antigens.
引用
收藏
页码:777 / 784
页数:8
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