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T淋巴细胞的抗原激活:主要组织相容性复合体的影响

Antigen activation of T lymphocytes: influence of major histocompatibility complex.

作者信息

Miller J F, Vadas M A

出版信息

Cold Spring Harb Symp Quant Biol. 1977;41 Pt 2:579-88. doi: 10.1101/sqb.1977.041.01.067.

Abstract

There is considerable evidence that T-cell activation to soluble antigens occurs only if this is processed by macrophages and displayed appropiately on the cell membrane in association with products of the genes of the MHC. The genes responsible differ according to the cells and antigens involved. For cytotoxicity, targets and killer T cells must share K- or D-region gene products. For delayed-type hypersensitivity to FGG in mice, I-A identity is necessary; for DNFB, identity at either the I, K, or D region is sufficient. Experiments using three different approaches do not support the notion that these genetic constraints are due to the necessity for the T cell and stimulator cell to match an identical gene product or cell-interaction molecule. Rather, they favor the hypothesis that there are receptors on the activated T cell which recognize antigen and products of genes of the MHC. The implications of the results are discussed in terms of (1) different T-cell subsets, (2) the mode of action of Ir genes, and (3) the possible parallel evolution of T-cell receptors for antigen and gene products of the MHC.

摘要

有大量证据表明,T细胞只有在可溶性抗原被巨噬细胞处理并与主要组织相容性复合体(MHC)基因产物一起适当地展示在细胞膜上时,才会被激活。所涉及的基因因细胞和抗原而异。对于细胞毒性作用,靶细胞和杀伤性T细胞必须共享K区或D区基因产物。对于小鼠对卵纤蛋白原的迟发型超敏反应,I-A区相同是必要的;对于二硝基氟苯,I区、K区或D区的相同就足够了。使用三种不同方法进行的实验并不支持这样的观点,即这些遗传限制是由于T细胞和刺激细胞需要匹配相同的基因产物或细胞相互作用分子。相反,这些实验支持这样的假设,即活化的T细胞上存在识别抗原和MHC基因产物的受体。我们将根据(1)不同的T细胞亚群、(2)免疫反应基因的作用方式以及(3)抗原T细胞受体与MHC基因产物可能的平行进化来讨论这些结果的意义。

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