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首页> 外文期刊>The Journal of Experomental Medicine >Cytotoxic T lymphocyte nonresponsiveness to the male antigen H-Y in the H-2Db mutants bm13 and bm14. Complementation of the response in F1 crosses with the I-Ab mutant bm12 nonresponder and failure of B6 or Db mutant mice tolerant of each other to respond to allogeneic male cells.
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Cytotoxic T lymphocyte nonresponsiveness to the male antigen H-Y in the H-2Db mutants bm13 and bm14. Complementation of the response in F1 crosses with the I-Ab mutant bm12 nonresponder and failure of B6 or Db mutant mice tolerant of each other to respond to allogeneic male cells.

机译:H-2Db突变体bm13和bm14对男性抗原H-Y的细胞毒性T淋巴细胞无反应性。 F1中的应答与I-Ab突变体bm12无应答者杂交,并且B6或Db突变体小鼠彼此耐受对同种异体雄性细胞的应答失败。

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The cytotoxic T-lymphocyte (CTL) response against the male-specific antigen H-Y in C57BL/6 (B6, H-2b) mice is regulated by the I-Ab and Db molecules. From previous studies, we concluded that the bm12 I-Ab mutant does not respond to H-Y, because of a deletion in its T-helper-cell repertoire. We now demonstrate that two Db mutants, bm13 and bm14, also fail to generate a CTL response to H-Y. The bm12 class-II mutant on one hand and the bm13 and bm14 class-I mutants on the other complemented each other for the H-Y-specific CTL response in (bm12 X bm13)F1 and (bm 12 X bm 14)F1 hybrids. This indicates that the need for tolerance of the mutant class II and class I molecules in these hybrids does not create deletions in the I-Ab-restricted T helper cell and Db-restricted CTL repertoire for H-Y. This study constitutes the first demonstration with H-2 mutants that a CTL response controlled by class I and class II MHC molecules is complemented in an F1 cross between a class I and a class II nonresponder. (B6 X bm 13)F1 and (B6 X bm 14)F1 hybrids only responded to H-Y when the antigen was presented on F1 or B6 antigen-presenting cells (apc) but not on Db mutant apc. B6 or Db mutant responders rendered neonatally tolerant of each other failed to respond to the H-Y antigen presented on the tolerogenic allogeneic cell. In the tolerized animals, a response was only seen with responder (B6) type T cells and responder type (B6) apc, indicating that both the T cell source and the MHC type of the apc have to be taken into account in this system. Thus, Ir genes may act at the level of both the T cell repertoire and antigen presentation.
机译:I-Ab和Db分子可调节C57BL / 6(B6,H-2b)小鼠对雄性特异性抗原H-Y的细胞毒性T淋巴细胞(CTL)反应。从以前的研究中,我们得出结论,bm12 I-Ab突变体不响应H-Y,因为其T辅助细胞库中存在缺失。现在,我们证明了两个Db突变体bm13和bm14也无法生成对H-Y的CTL反应。一方面bm12 II类突变体,另一方面bm13和bm14 I类突变体在(bm12 X bm13)F1和(bm 12 X bm 14)F1杂种中对H-Y特异的CTL反应相互补充。这表明在这些杂种中对突变的II类和I类分子的耐受性需求不会在H-Y的I-Ab限制的T辅助细胞和Db限制的CTL库中产生缺失。这项研究用H-2突变体首次证明了由I类和II类MHC分子控制的CTL反应在I类和II类无反应者之间的F1杂交中得到了补充。 (B6 X bm 13)F1和(B6 X bm 14)F1杂种仅在抗原存在于F1或B6抗原呈递细胞(apc)上而不对Db突变apc呈递时才响应H-Y。彼此具有新生儿耐受性的B6或Db突变体应答者无法对耐受性同种异体细胞上呈现的H-Y抗原产生应答。在耐受的动物中,仅对应答者(B6)型T细胞和应答者类型(B6)apc可见应答,表明在该系统中必须同时考虑apc的T细胞来源和MHC类型。因此,Ir基因可以在T细胞库和抗原呈递的水平上起作用。

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