Differences in Shared T Cell receptor α Repertoire Associated with Recognition of Viral Antigens.

IF 2.3 4区 医学 Q3 IMMUNOLOGY
Immunological Investigations Pub Date : 2026-05-01 Epub Date: 2026-03-16 DOI:10.1080/08820139.2026.2644288
Tiitus Lamponen, Joonatan Mattila, Nelli Heikkilä, Silja Sormunen, Jari Saramäki, T Petteri Arstila
{"title":"Differences in Shared T Cell receptor α Repertoire Associated with Recognition of Viral Antigens.","authors":"Tiitus Lamponen, Joonatan Mattila, Nelli Heikkilä, Silja Sormunen, Jari Saramäki, T Petteri Arstila","doi":"10.1080/08820139.2026.2644288","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Despite the high diversity of the αβ T cell receptor (TCR), sharing of identical TCR chains between individuals is common. This shared repertoire consists mainly of chains with few non-germline nucleotide additions. Many of these chains recognize conserved viral peptides, but it is unclear whether the number of nucleotide additions is similar regardless of specificity.</p><p><strong>Methods: </strong>We studied shared human TCR α chains associated with the recognition of viral antigens. The chains were retrieved from published databases. In sets of 6 thymus and 10 blood samples we identified these chains and analyzed their frequency and properties in the pre-immune and peripheral repertoire.</p><p><strong>Results: </strong>For all but one virus, the identified TCR α sequences conformed to the conventional public repertoire, with a high frequency of germline rearrangements and few nucleotide additions. Surprisingly, TCR α sequences associated with Herpes simplex virus 2 (HSV-2) displayed a bimodal division, with one group of sequences having a high number of inserts, while the other group was close to germline.</p><p><strong>Conclusion: </strong>Our results identify a novel type of shared TCR repertoire, likely to be generated by selection instead of convergent recombination. Whether this reflects features exclusive to the immune response against HSV-2 remains to be studied.</p>","PeriodicalId":13387,"journal":{"name":"Immunological Investigations","volume":" ","pages":"718-733"},"PeriodicalIF":2.3000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunological Investigations","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/08820139.2026.2644288","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/16 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Despite the high diversity of the αβ T cell receptor (TCR), sharing of identical TCR chains between individuals is common. This shared repertoire consists mainly of chains with few non-germline nucleotide additions. Many of these chains recognize conserved viral peptides, but it is unclear whether the number of nucleotide additions is similar regardless of specificity.

Methods: We studied shared human TCR α chains associated with the recognition of viral antigens. The chains were retrieved from published databases. In sets of 6 thymus and 10 blood samples we identified these chains and analyzed their frequency and properties in the pre-immune and peripheral repertoire.

Results: For all but one virus, the identified TCR α sequences conformed to the conventional public repertoire, with a high frequency of germline rearrangements and few nucleotide additions. Surprisingly, TCR α sequences associated with Herpes simplex virus 2 (HSV-2) displayed a bimodal division, with one group of sequences having a high number of inserts, while the other group was close to germline.

Conclusion: Our results identify a novel type of shared TCR repertoire, likely to be generated by selection instead of convergent recombination. Whether this reflects features exclusive to the immune response against HSV-2 remains to be studied.

与病毒抗原识别相关的共享T细胞受体α库的差异
背景:尽管αβ T细胞受体(TCR)具有高度多样性,但个体之间共享相同的TCR链是很常见的。这种共享的基因库主要由一些非种系核苷酸添加的链组成。许多这些链识别保守的病毒肽,但不清楚核苷酸添加的数量是否相似,而不考虑特异性。方法:研究与病毒抗原识别相关的人类共有的TCR α链。这些链是从已发布的数据库中检索的。在6个胸腺和10个血液样本中,我们确定了这些链,并分析了它们在免疫前和外周血库中的频率和特性。结果:除一种病毒外,鉴定的TCR α序列均符合常规公共库,种系重排频率高,核苷酸添加量少。令人惊讶的是,与单纯疱疹病毒2 (HSV-2)相关的TCR α序列显示出双峰分裂,其中一组序列具有大量插入,而另一组序列接近种系。结论:我们的研究结果确定了一种新型的共享TCR库,可能是通过选择而不是聚合重组产生的。这是否反映了针对HSV-2的免疫反应的独有特征仍有待研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Immunological Investigations
Immunological Investigations 医学-免疫学
CiteScore
5.50
自引率
7.10%
发文量
49
审稿时长
3 months
期刊介绍: Disseminating immunological developments on a worldwide basis, Immunological Investigations encompasses all facets of fundamental and applied immunology, including immunohematology and the study of allergies. This journal provides information presented in the form of original research articles and book reviews, giving a truly in-depth examination of the latest advances in molecular and cellular immunology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书