Circulating effector γδ T cell populations are associated with acute coronavirus disease 19 in unvaccinated individuals

IF 3.2 4区 医学 Q3 CELL BIOLOGY
Anouk von Borstel, Thi HO Nguyen, Louise C Rowntree, Thomas M Ashhurst, Lilith F Allen, Lauren J Howson, Natasha E Holmes, Olivia C Smibert, Jason A Trubiano, Claire L Gordon, Allen C Cheng, Stephen J Kent, Jamie Rossjohn, Katherine Kedzierska, Martin S Davey
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Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causes severe coronavirus disease 2019 (COVID-19) in a small proportion of infected individuals. The immune system plays an important role in the defense against SARS-CoV-2, but our understanding of the cellular immune parameters that contribute to severe COVID-19 disease is incomplete. Here, we show that populations of effector γδ T cells are associated with COVID-19 in unvaccinated patients with acute disease. We found that circulating CD27negCD45RA+CX3CR1+ Vδ1effector cells expressing Granzymes (Gzms) were enriched in COVID-19 patients with acute disease. Moreover, higher frequencies of GzmB+ Vδ2+ T cells were observed in acute COVID-19 patients. SARS-CoV-2 infection did not alter the γδ T cell receptor repertoire of either Vδ1+ or Vδ2+ subsets. Our work demonstrates an association between effector populations of γδ T cells and acute COVID-19 in unvaccinated individuals.

Abstract Image

循环效应γδ T细胞群与未接种疫苗个体急性冠状病毒病19相关
严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染在一小部分感染者中引起2019年严重冠状病毒病(COVID-19)。免疫系统在防御SARS-CoV-2中发挥着重要作用,但我们对导致严重COVID-19疾病的细胞免疫参数的理解尚不完整。本研究表明,在未接种疫苗的急性疾病患者中,效应γδ T细胞群与COVID-19相关。我们发现循环CD27negCD45RA+CX3CR1+表达颗粒酶(Granzymes, Gzms)的v δ1效应细胞在COVID-19急性疾病患者中富集。此外,急性COVID-19患者中GzmB+ Vδ2+ T细胞的频率更高。SARS-CoV-2感染没有改变Vδ1+或Vδ2+亚群的γδ T细胞受体库。我们的研究表明,未接种疫苗的个体中γδ T细胞效应群与急性COVID-19之间存在关联。
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来源期刊
Immunology & Cell Biology
Immunology & Cell Biology 医学-免疫学
CiteScore
7.50
自引率
2.50%
发文量
98
审稿时长
4-8 weeks
期刊介绍: The Australasian Society for Immunology Incorporated (ASI) was created by the amalgamation in 1991 of the Australian Society for Immunology, formed in 1970, and the New Zealand Society for Immunology, formed in 1975. The aim of the Society is to encourage and support the discipline of immunology in the Australasian region. It is a broadly based Society, embracing clinical and experimental, cellular and molecular immunology in humans and animals. The Society provides a network for the exchange of information and for collaboration within Australia, New Zealand and overseas. ASI members have been prominent in advancing biological and medical research worldwide. We seek to encourage the study of immunology in Australia and New Zealand and are active in introducing young scientists to the discipline.
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