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由H-2控制的E分子激活的细胞溶解性T细胞与A分子发生交叉反应。

Cytolytic T cells activated by H-2-controlled E molecules cross-react with A molecules.

作者信息

Vucak I, Juretić A, Nagy Z A, Klein J

出版信息

Immunogenetics. 1982;15(5):519-27. doi: 10.1007/BF00345911.

Abstract

Cell-mediated lymphocytotoxicity was generated in four strain combinations differing only by the cell-surface expression of the class II E molecule controlled by the H-2 complex. The four combinations were: B10.D2(R107) anti-B10.A(3R), B10.A(4R) anti-B10.A(2R), B10.GD anti-B10.D2(R101), and B10.S(7R) anti-B10.S(9R). In all four of these combinations, the stimulator expresses E molecules on the cell surface, while the responder does not. The cytolytic T lymphocytes generated in the B10.D2(R107) anti-B10.A(3R) and B10.A(4R) anti-B10.A(2R) combinations reacted not only with the stimulator but also with strains that do not express cell-surface E molecules, in particular, strains carrying the H-2f and H-2q haplotypes. The cross-reactivity with E-negative strains could be blocked by monoclonal antibodies specific for the Af or Aq molecules but not by antibodies recognizing determinants on E or class I (K) molecules. The anti-H-2f cross-reactivity could be inhibited by H-2q cold targets and, reciprocally, the anti-H-2q reactivity could be blocked by H-2f cold targets. These findings are interpreted as indicating that the cytolytic T lymphocytes stimulated by E molecules can recognize and lyse cells lacking E molecules but expressing A molecules. The observed E-A cross-reactivity supports the notion of structural and functional relatedness between the A and E molecules and suggests a common evolutionary origin of the A- and E-encoding loci.

摘要

细胞介导的淋巴细胞毒性在仅因由H-2复合体控制的II类E分子的细胞表面表达而不同的四种品系组合中产生。这四种组合是:B10.D2(R107)抗B10.A(3R)、B10.A(4R)抗B10.A(2R)、B10.GD抗B10.D2(R101)和B10.S(7R)抗B10.S(9R)。在所有这四种组合中,刺激细胞在细胞表面表达E分子,而反应细胞则不表达。在B10.D2(R107)抗B10.A(3R)和B10.A(4R)抗B10.A(2R)组合中产生的细胞毒性T淋巴细胞不仅与刺激细胞反应,而且还与不表达细胞表面E分子的品系反应,特别是携带H-2f和H-2q单倍型的品系。与E阴性品系的交叉反应性可被针对Af或Aq分子的单克隆抗体阻断,但不能被识别E或I类(K)分子上决定簇的抗体阻断。抗H-2f交叉反应性可被H-2q冷靶抑制,反之,抗H-2q反应性可被H-2f冷靶阻断。这些发现被解释为表明由E分子刺激的细胞毒性T淋巴细胞可以识别并裂解缺乏E分子但表达A分子的细胞。观察到的E-A交叉反应性支持了A和E分子之间结构和功能相关性的概念,并表明A和E编码基因座有共同的进化起源。

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