癌症中的双 TCR 表达 T 细胞:单细胞技术如何实现新的研究。

Elizabeth M Muhowski, Laura M Rogers
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引用次数: 0

摘要

TCR 多样性测量通常用于了解癌症的免疫反应。传统的多样性测量方法依赖于对 β 链可变区的大量 RNA 测序(RNAseq)。然而,完整的 αβ TCR 反应谱系是由α链和β链组合而成的,而α链和β链分别由不同的基因编码。与批量 RNAseq 相比,单细胞 RNAseq(scRNAseq)可进行配对链分析,从而更准确地测量基因库。有趣的是,30% 的成熟外周 T 细胞表达多个 TCR 等位基因(如两条 α 链),可能表现出双重 Ag 特异性。然而,常规工作流程会摒弃次级 TCR 等位基因,只关注每个细胞的单个 TCR 克隆。这篇视角文章强调了为什么这可能不是好的做法,并着重指出了 T 细胞双重特异性领域的未解之谜。
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Dual TCR-Expressing T Cells in Cancer: How Single-Cell Technologies Enable New Investigation.

TCR diversity measures are often used to understand the immune response in cancer. Traditional measures of diversity rely on bulk RNA sequencing (RNAseq) of the β-chain variable regions. However, the full αβ TCR repertoire is a combination of both the α- and β-chains, which are encoded by separate genes. In contrast with bulk RNAseq, single-cell RNAseq (scRNAseq) allows paired chain analyses, yielding a more accurate measure of the repertoire. Interestingly, ∼30% of mature peripheral T cells express multiple TCR alleles (e.g., two α-chains) and may exhibit dual Ag specificity. scRNAseq has become increasingly common, and data from both human and animal studies are publicly available. However, routine workflows discard secondary TCR alleles and focus on a single TCR clone per cell. This perspectives piece emphasizes why this may not be good practice and highlights unanswered questions in the field of T cell dual specificity.

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