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H-2对针对单一非H-2同种异体抗原反应中细胞间相互作用的影响。V. H-2Kb突变对H-4和H-3同种异体抗原呈递的影响。

H-2 effects on cell-cell interactions in the response to single non-H-2 alloantigens. V. Effects of H-2Kb mutations on presentation of H-4 and H-3 alloantigens.

作者信息

Wettstein P J

出版信息

J Immunol. 1982 Jun;128(6):2629-33.

PMID:6978909
Abstract

The effects of a panel of H-2Kb mutants on the presentation of the non-H-2 histocompatibility (H) antigens H-4.2 and H-3.1 to antigen-specific T cells were examined. Kb-restricted cytotoxic effector T cells were presented with H-4.2 and H-3.1 in the context of mutant Kb alleles. H-4.2 was differentially presented by Kb mutants to Kb-restricted cytotoxic effectors. Cold target inhibition analysis demonstrated that Kb-restricted, H-4.2-specific cytotoxic effectors recognized H-4.2 in the context of at least three restriction sites on the Kb molecule. One site is specific for Kb alone, whereas two additional sites are differentially expressed by Kb mutant molecules. The effect of Kb mutations on the presentation of H-4.2 and H-3.1 was H antigen-specific. Identical, respective patterns of presentation of H-4.2 and H-3.1 by Kb mutants were observed with Kb-restricted T cells proliferating in secondary mixed lymphocyte culture. Further, individual mice varied in their preference for H-3.1 presented in the context of different Kb mutant molecules. These observations demonstrate that the presentation of H antigens by mutant Kb molecules is antigen-specific; analysis of presentation of H antigen by mutants to wild-type Kb-restricted effectors allows the identification of multiple restriction sites on the Kb molecule.

摘要

检测了一组H-2Kb突变体对非H-2组织相容性(H)抗原H-4.2和H-3.1向抗原特异性T细胞提呈的影响。在突变Kb等位基因的背景下,向Kb限制性细胞毒性效应T细胞提呈H-4.2和H-3.1。Kb突变体对Kb限制性细胞毒性效应细胞以不同方式提呈H-4.2。冷靶抑制分析表明,Kb限制性、H-4.2特异性细胞毒性效应细胞在Kb分子上至少三个限制性位点的背景下识别H-4.2。一个位点仅对Kb具有特异性,而另外两个位点在Kb突变体分子中差异表达。Kb突变对H-4.2和H-3.1提呈的影响具有H抗原特异性。在二次混合淋巴细胞培养中增殖的Kb限制性T细胞观察到Kb突变体对H-4.2和H-3.1的提呈模式分别相同。此外,不同小鼠对在不同Kb突变体分子背景下提呈的H-3.1的偏好各不相同。这些观察结果表明,突变Kb分子对H抗原的提呈具有抗原特异性;分析突变体对野生型Kb限制性效应细胞的H抗原提呈可确定Kb分子上的多个限制性位点。

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