Identification and characterization of Xenopus CD8+ T cells expressing an NK cell-associated molecule

被引:0
|
作者
Rau, L
Gantress, J
Bell, A
Stewart, R
Horton, T
Cohen, N
Horton, J
Robert, J
机构
[1] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[2] Univ Durham, Sch Biol & Biomed Sci, Durham DH1 3HP, England
关键词
CD8(+); NK/T cell; NK cell-associated molecule; Xenopus;
D O I
10.1002/1521-4141(200206)32:6<1574::AID-IMMU1574>3.0.CO;2-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Growing evidence suggests that some immune responses are mediated not only by conventional and distinct NK cells and CTL, but also by T cell subsets expressing NK receptors and NK cell-associated molecules. Consistent with our previously published finding that the mAb 1F8 identifies non-T/non-B cells in Xenopus that effect NK-like killing in vitro, we now report that in vivo treatment with this mAb impairs rejection of transplanted MHC class I-negative tumor cells. However, we also find that the NK cell-associated molecule recognized by mAb 1F8 is expressed by a minor population of CD8(+) T cells, in which fully rearranged TCRP mRNA of at least three different V families can be identified, by contrast, 1F8(+)/CD8(NK) cells lack such TCRP message. Additionally, the expression of the NK cell-associated molecule can be induced in vitro by a transient submitogenic stimulation of naive CD8(+) T cells with PMA and ionomycin. Such induced expression of 1F8 also occurs in alloantigen-activated CTL and is coincident with a down-regulation of MHC-specific cytotoxicity. Taken together, these new data suggest that regulation of CD8(+) T cell activity involving NK cell-associated molecules is a general and evolutionarily ancient phenomenon.
引用
收藏
页码:1574 / 1583
页数:10
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