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免疫反应遗传控制中的决定簇选择与巨噬细胞功能

Determinant selection and macrophage function in genetic control of the immune response.

作者信息

Rosenthal A S

出版信息

Immunol Rev. 1978;40:136-52. doi: 10.1111/j.1600-065x.1978.tb00404.x.

Abstract

The immune response to insulin, in both mouse and guinea pig, is under control of H-linked immune response genes. When immunized with either pork or beef insulin in CFA, both strain 2 and 13 guinea pigs respond by antigen-specific lymphocyte proliferation and synthesis of specific antibody. The specificities of the elicited antibodies and indistinguishable between these inbred strains. By constrast, strain 2 T cells recognized a distinct region of the A chain alpha loop consisting of amino acid residues 8, 9 and 10, while strain 13 T cells see an as yet undefined region of the B chain. H2b (A chain alpha loop responder) and H2d (B chain responder) mice similarly discriminate which areas of the molecule are recognized by their T lymphocytes. The function of the Ir gene in both the guinea pig and mouse appears to be an intramolecular selection of discrete regions within the antigen for recognition by the T cell. The data presented suggest that this function operates at the level of the macrophage.

摘要

在小鼠和豚鼠中,对胰岛素的免疫反应受H连锁免疫反应基因的控制。当用弗氏完全佐剂中的猪肉或牛肉胰岛素免疫时,2型和13型豚鼠均通过抗原特异性淋巴细胞增殖和特异性抗体的合成作出反应。所诱导抗体的特异性在这些近交系中是无法区分的。相比之下,2型T细胞识别由氨基酸残基8、9和10组成的A链α环的一个独特区域,而13型T细胞识别B链的一个尚未确定的区域。H2b(A链α环反应者)和H2d(B链反应者)小鼠同样能区分其T淋巴细胞识别分子的哪些区域。豚鼠和小鼠中Ir基因的功能似乎是在分子内选择抗原内的离散区域以供T细胞识别。所呈现的数据表明,该功能在巨噬细胞水平发挥作用。

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