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首页> 外文期刊>Molecular Immunology >T-cell receptor repertoires utilized in response to linear peptides representing an immunodominant MHC class II restricted T-cell epitope are far more diverse than that utilized in response to the same epitope in the nominal antigen.
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T-cell receptor repertoires utilized in response to linear peptides representing an immunodominant MHC class II restricted T-cell epitope are far more diverse than that utilized in response to the same epitope in the nominal antigen.

机译:用于响应代表免疫优势的II类MHC限制的T细胞表位的线性肽的T细胞受体库比用于响应标称抗原中相同表位的库的多样性要大得多。

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摘要

Previous analyses of the T-cell receptor (TCR) repertoire utilized in response to the 1-102 fragment of the lambda cI repressor protein and specific for the immunodominant amino acid 12-26 region in the context of I-Ek, have shown this repertoire to be extremely restricted. In contrast, here we show that the TCR repertoires utilized in two strains of I-Ek expressing mice in response to two linear peptides representing this immunodominant region are diverse. Despite their extensive diversity, these repertoires are somewhat overlapping. In addition, structural similarities were observed between the full lambda cI fragment (1-102) and peptide elicited TCR repertoires, including frequent use of the Valpha2 family of gene segments, particularly among peptide (12-26) elicited TCRs cross-reactive with 1-102/I-Ek. Nevertheless, these data indicate that it may be difficult to mimic the immune response to an immunodominant epitope of a protein antigen via immunization with linear peptides containing the amino acid sequence of that epitope. Possible explanations for differences in the levels of TCR diversity among T cells responding to an epitope present in a nominal antigen as compared to T cells responding to linear peptide antigens containing this same epitope are discussed.
机译:先前对响应lambda cI阻遏蛋白的1-102片段使用的T细胞受体(TCR)组成部分的分析,在I-Ek的背景下对免疫占主导地位的氨基酸12-26区具有特异性,已显示出该组成部分受到严格限制。相比之下,在这里我们显示了在两种表达I-Ek的小鼠品系中,响应代表该免疫优势区域的两个线性肽所使用的TCR谱是多种多样的。尽管种类繁多,这些曲目还是有些重叠。此外,在整个λcI片段(1-102)与肽诱导的TCR组成之间观察到结构相似性,包括频繁使用Valpha2家族的基因片段,特别是在肽(12-26)诱导的TCR与1交叉反应的情况下-102 / I-Ek。然而,这些数据表明,通过用包含该表位的氨基酸序列的线性肽进行免疫,可能难以模拟对蛋白质抗原的免疫优势表位的免疫应答。讨论了对应答标称抗原中存在的表位的T细胞与应答包含相同表位的线性肽抗原的T细胞相比,TCR多样性水平差异的可能解释。

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