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抑制性T细胞、免疫球蛋白和免疫球蛋白重链基因限制

Suppressor T cells, immunoglobulin and Igh restriction.

作者信息

Sy M S, Benacerraf B

机构信息

Department of Pathology, Harvard Medical School, Boston, MA 02115.

出版信息

Immunol Rev. 1988 Jan;101:133-48. doi: 10.1111/j.1600-065x.1988.tb00735.x.

Abstract

Why do some T cell express idiotypes that are serologically similar to those of the B cells, since it is now well established that T cells do not use Ig genes for their antigen specific receptors? In this review article, we have summarized some the evidence for the influence of Igh linked genes on the Suppressor T cell repertoire, using anti-u treated mice as a model system. We investigated whether B cells and Ig molecules play a role in the generation of Ts repertoire. While our results clearly confirmed that B cells and Ig are important in the establishment of Ts repertoire, our experiments failed to resolve the fundamental question - 'what dictates the Igh restriction specificity of Ts?' Ts cells from anti-u treated mice did not lose all Igh restriction specificity. Instead, they expressed an altered restriction specificity. These results suggest that there are at least two independent mechanisms responsible for the generation of the suppressor T cell repertoire. A pre-selected germ line one, which is Ig independent, and a mature one, which is Ig dependent. The precise mechanisms responsible for the generation of germ line Ts repertoire remain to be determined.

摘要

既然现在已经充分证实T细胞的抗原特异性受体并不使用Ig基因,那么为什么有些T细胞会表达与B细胞在血清学上相似的独特型呢?在这篇综述文章中,我们以抗μ处理的小鼠作为模型系统,总结了一些关于Igh连锁基因对抑制性T细胞库影响的证据。我们研究了B细胞和Ig分子在抑制性T细胞库产生过程中是否发挥作用。虽然我们的结果清楚地证实了B细胞和Ig在抑制性T细胞库的建立中很重要,但我们的实验未能解决这个基本问题——“是什么决定了抑制性T细胞的Igh限制性特异性?”来自抗μ处理小鼠的抑制性T细胞并没有丧失所有的Igh限制性特异性。相反,它们表达了一种改变的限制性特异性。这些结果表明,至少有两种独立的机制负责抑制性T细胞库的产生。一种是预先选择的种系机制,它不依赖于Ig,另一种是成熟机制,它依赖于Ig。负责种系抑制性T细胞库产生的确切机制仍有待确定。

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