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在显示II类主要组织相容性复合体结合自身肽库发生改变的小鼠中,CD4 T细胞的阳性选择缺陷。

Deficient positive selection of CD4 T cells in mice displaying altered repertoires of MHC class II-bound self-peptides.

作者信息

Grubin C E, Kovats S, deRoos P, Rudensky A Y

机构信息

Department of Immunology, University of Washington, Seattle 98195, USA.

出版信息

Immunity. 1997 Aug;7(2):197-208. doi: 10.1016/s1074-7613(00)80523-3.

Abstract

The role of self-peptides in positive selection of CD4+ T cells has been controversial. We show that some self-peptides are presented by the MHC class II molecule I-A(b) in mice lacking Ii or H-2M but not in mice expressing a transgene-encoded peptide fused to I-A(b). In experiments using specific antibodies to block selection, these low-abundance self-peptides were implicated in the positive selection of some CD4+ T cells in H-2M-/- mice. However, all three mutant backgrounds failed to positively select two class II-restricted transgenic T cell receptors. Our findings suggest that minor components of the self-peptide repertoire can contribute to positive selection of a significant number of CD4+ T cells. In addition, the data suggest that T cell receptor repertoires selected in wild-type mice and in mice displaying limited spectra of self-peptides are distinct.

摘要

自身肽在CD4⁺T细胞阳性选择中的作用一直存在争议。我们发现,在缺乏Ii或H-2M的小鼠中,一些自身肽由MHC II类分子I-A(b)呈递,但在表达与I-A(b)融合的转基因编码肽的小鼠中则不然。在使用特异性抗体阻断选择的实验中,这些低丰度自身肽与H-2M⁻/⁻小鼠中一些CD4⁺T细胞的阳性选择有关。然而,所有三种突变背景均未能对两种II类限制性转基因T细胞受体进行阳性选择。我们的研究结果表明,自身肽库的次要成分可有助于大量CD4⁺T细胞的阳性选择。此外,数据表明在野生型小鼠和显示有限自身肽谱的小鼠中选择的T细胞受体库是不同的。

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