首页> 美国卫生研究院文献>The Journal of Experimental Medicine >H-2 compatability requirement for T-cell-mediated lysis of target cells infected with lymphocytic choriomeningitis virus. Different cytotoxic T- cell specificities are associated with structures coded for in H-2K or H-2D;
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H-2 compatability requirement for T-cell-mediated lysis of target cells infected with lymphocytic choriomeningitis virus. Different cytotoxic T- cell specificities are associated with structures coded for in H-2K or H-2D;

机译:H-2相容性要求用于感染淋巴细胞性脉络膜脑膜炎病毒的目标细胞的T细胞介导裂解。不同的细胞毒性T细胞特异性与H-2K或H-2D中编码的结构有关;

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摘要

Use of syngeneic, allogeneic, F1, AND H-2 recombinatn mice has shown that animals injected with lymphocytic choriomeningitis (LCM) virus generate T cells which are cytotoxic for H-2K or H-2D compatible, but not H-2 different, virus-infected target cells. Three separate lines of evidence are presented which indicate that these immune T cells are sensitized to "altered-self," the self antigens involved being coded for in the H-2K or H-2d regions. Firstly, cytotoxic activity associated with mutuality at H-2D iy, lysis mediated by immune T cells from F1 or H-2 recombinant mice is specifically inhibited only by presence of unlabeled, virus-infected cells that are H-2 compatible with the targets. Thirdly, LCM-immune F1 and H-2 recombinant T cells inoculated into irradiated, virus-infected recipients proliferate only to kill target cells that are H-2 compatible with both the donor and the recipient. All of these experiments establish that there is a dissociation of T-cell activities between parental haplotypes in F1 mice, and between H-2K and H-2D in recombinants. It would thus seem that there are at least two specificities of tlcm-immune T cells in homozygotes, associated with either H-2K or H-2D, and four specificities in F1 hybrids. The significance of these findings, with respect both to gene duplication and to the marked polymorphism in the H-2 system, is discussed.
机译:使用同基因,同种异体,F1和H-2重组小鼠已显示,注射淋巴细胞性脉络膜脑膜炎(LCM)病毒的动物产生的T细胞对H-2K或H-2D相容但对H-2不同的病毒具有细胞毒性感染的靶细胞。提出了三个单独的证据线,表明这些免疫T细胞对“改变的自身”敏感,涉及的自身抗原在H-2K或H-2d区域编码。首先,与F-2或H-2重组小鼠的免疫T细胞介导的H-2D y裂解相关的细胞毒性活性仅通过存在与靶标H-2相容的未标记病毒感染细胞而被特异性抑制。第三,接种到受辐照,病毒感染的受体中的免疫LCM的F1和H-2重组T细胞只会增殖以杀死与供体和受体都兼容的H-2靶细胞。所有这些实验都确定,F1小鼠的亲本单倍型之间以及重组子中的H-2K和H-2D之间存在T细胞活性的解离。因此,似乎纯合子中具有与H-2K或H-2D相关的tcm1免疫T细胞的至少两种特异性,以及在F1杂种中具有四种特异性。讨论了这些发现的意义,就基因复制和H-2系统中明显的多态性而言。

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