von Borstel, Anouk, Nguyen, Thi HO, Rowntree, Louise C, Ashhurst, Thomas M, Allen, Lilith F, Howson, Lauren J, Holmes, Natasha E, Smibert, Olivia C, Trubiano, Jason A, Gordon, Claire L, Cheng, Allen C, Kent, Stephen J, Rossjohn, Jamie ORCID: https://orcid.org/0000-0002-2020-7522, Kedzierska, Katherine and Davey, Martin S 2023. Circulating effector γδ T cell populations are associated with acute coronavirus disease 19 in unvaccinated individuals. Immunology & Cell Biology 10.1111/imcb.12623 |
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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.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Medicine |
Additional Information: | License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/ |
Publisher: | Wiley |
ISSN: | 0818-9641 |
Date of First Compliant Deposit: | 20 February 2023 |
Date of Acceptance: | 23 January 2023 |
Last Modified: | 03 May 2023 07:46 |
URI: | https://orca.cardiff.ac.uk/id/eprint/157149 |
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