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T淋巴细胞对化学定义抗原反应的特异性。

The specificity of T lymphocyte responses to chemically defined antigens.

作者信息

Janeway C A

出版信息

Transplant Rev. 1976;29:164-88. doi: 10.1111/j.1600-065x.1976.tb00201.x.

Abstract

A system is described that allows the definition of T cell receptor specificity with some precision. It involves immunization of guinea pigs with hapten coupled to mycobacteria. The T cells of such animals respond to many but not all carriers modified by that hapten. Such T cells recognize neither hapten nor carrier alone, but rather determinants involving both the hapten and the carrier. No evidence for hapten-specific T cells was found. A model of the antigen binding site of the T cell receptor emerged from these experiments. According to this model, the T cell receptor consists of a single site of relatively large extent involving multiple subsites which are of low and roughly equal affinity. Thus, the haptenic group is not immunodominant for T cells as it is for B cells and for anti-hapten antibody. This suggests that the antigen binding receptor on T cells differs in some fundamental way from that on B cells. It is proposed that antigen recognition by T cells is mediated by an immunoglobulin heavy chain variable region that is not paired with an immunoglobulin light chain variable region.

摘要

描述了一种能够较为精确地定义T细胞受体特异性的系统。该系统涉及用与分枝杆菌偶联的半抗原免疫豚鼠。这类动物的T细胞会对许多但并非所有经该半抗原修饰的载体产生反应。此类T细胞既不单独识别半抗原也不单独识别载体,而是识别涉及半抗原和载体两者的决定簇。未发现半抗原特异性T细胞的证据。从这些实验中得出了T细胞受体抗原结合位点的模型。根据该模型,T细胞受体由一个范围相对较大的单一位点组成,该位点涉及多个亲和力较低且大致相等的亚位点。因此,半抗原基团对T细胞不像对B细胞和抗半抗原抗体那样具有免疫优势。这表明T细胞上的抗原结合受体在某些基本方面与B细胞上的不同。有人提出,T细胞的抗原识别是由一个未与免疫球蛋白轻链可变区配对的免疫球蛋白重链可变区介导的。

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