Suppr超能文献

通过半不变TCR-α链实现与MHC相关蛋白1限制的癌症识别。

MHC-related protein 1-restricted recognition of cancer via a semi-invariant TCR-α chain.

作者信息

Dolton Garry, Thomas Hannah, Tan Li Rong, Rius Rafael Cristina, Doetsch Stephanie, Ionescu Giulia-Andreea, Cardo Lucia F, Crowther Michael D, Behiry Enas, Morin Théo, Caillaud Marine E, Srai Devinder, Parolini Lucia, Hasan Md Samiul, Fuller Anna, Topley Katie, Wall Aaron, Hopkins Jade R, Omidvar Nader, Alvares Caroline, Zabkiewicz Joanna, Frater John, Szomolay Barbara, Sewell Andrew K

机构信息

Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.

Nuffield Department of Medicine and Department of Chemistry, University of Oxford, Oxford, United Kingdom.

出版信息

J Clin Invest. 2025 Jan 2;135(1):e181895. doi: 10.1172/JCI181895.

Abstract

The T cell antigen presentation platform MR1 consists of 6 allomorphs in humans that differ by no more than 5 amino acids. The principal function of this highly conserved molecule involves presenting microbial metabolites to the abundant mucosal-associated invariant T (MAIT) cell subset. Recent developments suggest that the role of MR1 extends to presenting antigens from cancer cells, a function dependent on the K43 residue in the MR1 antigen binding cleft. Here, we successfully cultured cancer-activated, MR1-restricted T cells from multiple donors and confirmed that they recognized a wide range of cancer types expressing the most common MR101 and/or MR102 allomorphs (over 95% of the population), while remaining inert to healthy cells including healthy B cells and monocytes. Curiously, in all but one donor these T cells were found to incorporate a conserved TCR-α chain motif, CAXYGGSQGNLIF (where X represents 3-5 amino acids), because of pairing between 10 different TRAV genes and the TRAJ42 gene segment. This semi-invariance in the TCR-α chain is reminiscent of MAIT cells and suggests recognition of a conserved antigen bound to K43.

摘要

T细胞抗原呈递平台MR1在人类中有6种同种异型,它们之间的差异不超过5个氨基酸。这种高度保守的分子的主要功能是将微生物代谢产物呈递给大量的黏膜相关恒定T(MAIT)细胞亚群。最近的研究进展表明,MR1的作用扩展到呈递癌细胞的抗原,这一功能依赖于MR1抗原结合裂隙中的K43残基。在这里,我们成功地从多个供体中培养出癌症激活的、受MR1限制的T细胞,并证实它们识别多种表达最常见的MR101和/或MR102同种异型(超过95%的人群)的癌症类型,而对包括健康B细胞和单核细胞在内的健康细胞保持惰性。奇怪的是,除了一名供体外,在所有供体中都发现这些T细胞包含一个保守的TCR-α链基序,CAXYGGSQGNLIF(其中X代表3至5个氨基酸),这是由于10个不同的TRAV基因与TRAJ42基因片段配对所致。TCR-α链的这种半不变性让人联想到MAIT细胞,并提示其识别与K43结合的保守抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b083/11684821/7526b563477f/jci-135-181895-g058.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验