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首页> 外文期刊>Trends in immunology >Self-recognition and the biased mature repertoire in TCR beta transgenic mice: the exception that supports the rule.
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Self-recognition and the biased mature repertoire in TCR beta transgenic mice: the exception that supports the rule.

机译:TCR beta转基因小鼠的自我认知能力和成熟的偏好库:支持该规则的例外。

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摘要

Detailed sequence analysis of the companion alpha chains in several T-cell receptor (TCR) beta chain transgenic mice have shown that the mature alpha chain repertoires of CD4(+) T cells are biased toward the parental TCR alpha chain sequences. These studies further indicate that it is self-peptide-self-MHC recognition during positive intrathymic selection that biases the structure of the mature TCR alpha chain repertoire. To further establish the causative relationship, it is important to examine whether such a bias can be abolished when positive selection is absent. The human collagen IV-I-A(s) complex-specific KB TCR cannot be positively selected on the self-peptide-self-MHC complexes present in the I-A(s) strain. Therefore, the KB TCR beta chain transgenic mice offer a unique opportunity for addressing this issue.
机译:几个T细胞受体(TCR)β链转基因小鼠中的陪伴alpha链的详细序列分析表明,CD4(+)T细胞的成熟alpha链库偏向亲本TCR alpha链序列。这些研究进一步表明,在胸腺内阳性选择过程中,自身肽-自身-MHC识别会偏向成熟TCRα链组成部分的结构。为了进一步建立因果关系,重要的是要检查在没有正面选择的情况下这种偏见是否可以消除。人胶原蛋白IV-I-A复合物特异性KB TCR不能在I-A菌株中存在的自身肽-自身-MHC复合物上阳性选择。因此,KB TCRβ链转基因小鼠为解决此问题提供了独特的机会。

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