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首页> 外文期刊>The Journal of Experomental Medicine >An immunodominant class I-restricted cytotoxic T lymphocyte determinant of human immunodeficiency virus type 1 induces CD4 class II-restricted help for itself.
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An immunodominant class I-restricted cytotoxic T lymphocyte determinant of human immunodeficiency virus type 1 induces CD4 class II-restricted help for itself.

机译:人类免疫缺陷病毒1型的主要免疫I类限制的细胞毒性T淋巴细胞决定因子自身诱导CD4 II类限制的帮助。

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摘要

We have observed that a peptide corresponding to an immunodominant epitope of the HIV-1 envelope protein recognized by class I MHC-restricted CD8+ CTL can also induce T cell help for itself. The help is necessary for restimulation of CTL precursors in vitro with peptide alone in the absence of exogenous lymphokines, can be removed by depletion of CD4+ T cells, and can be replaced by exogenous IL-2. Whereas the CTL in BALB/c or B10. D2 mice are restricted by the class I molecule Dd, the Th cells are restricted by the class II molecule Ad, and the help can be blocked by anti-Ad mAb. To examine the genetic regulation of the induction of help, we studied B10.A mice that share the class I Dd molecule, but have different class II molecules, Ak and Ek. Spleen cells of immune B10.A mice behave like CD4-depleted BALB/c spleen cells in that they cannot be restimulated in vitro by the peptide alone, but can with peptide plus IL-2. Therefore, in the absence of exogenous lymphokines, peptide-specific help is necessary for restimulation with this immunodominant CTL epitope peptide, and in H-2d mice, this peptide stimulates help for itself as well as CTL. We speculate on the implications of these findings for the immunodominance of this peptide in H-2d mice, and for the selective advantage of pairing certain class I and class II molecules in an MHC haplotype.
机译:我们已经观察到,与I类MHC限制性CD8 + CTL识别的HIV-1包膜蛋白的免疫优势表位相对应的肽本身也可以诱导T细胞的帮助。在不存在外源性淋巴因子的情况下,仅使用肽在体外对CTL前体进行再刺激是必要的,可以通过耗竭CD4 + T细胞将其清除,并可以用外源性IL-2替代。而BALB / c或B10中的CTL。 D2小鼠受到I类分子Dd的限制,Th细胞受到II类分子Ad的限制,并且该帮助可以被抗Ad mAb阻断。为了检查诱导帮助的遗传调控,我们研究了共享I类Dd分子但具有不同II类分子Ak和Ek的B10.A小鼠。免疫B10的脾脏细胞的行为类似于CD4耗竭的BALB / c脾脏细胞,它们不能单独由肽在体外再刺激,而可以由肽加IL-2来再刺激。因此,在不存在外源性淋巴因子的情况下,使用该免疫优势的CTL表位肽进行再刺激需要肽特异性帮助,并且在H-2d小鼠中,该肽可刺激自身以及CTL的帮助。我们推测这些发现对H-2d小鼠中该肽的免疫优势以及在MHC单倍型中配对某些I类和II类分子的选择性优势的意义。

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