Nature Communications (May 2024)

Cytomegalovirus drives Vδ1+ γδ T cell expansion and clonality in common variable immunodeficiency

  • Samantha Chan,
  • Benjamin Morgan,
  • Michelle K. Yong,
  • Mai Margetts,
  • Anthony J. Farchione,
  • Erin C. Lucas,
  • Jack Godsell,
  • Nhi Ai Giang,
  • Charlotte A. Slade,
  • Anouk von Borstel,
  • Vanessa L. Bryant,
  • Lauren J. Howson

DOI
https://doi.org/10.1038/s41467-024-48527-3
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 13

Abstract

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Abstract The function and phenotype of γδ T cells in the context of common variable immunodeficiency (CVID) has not been explored. CVID is a primary immunodeficiency disorder characterized by impaired antibody responses resulting in increased susceptibility to infections. γδ T cells are a subset of unconventional T cells that play crucial roles in host defence against infections. In this study, we aim to determine the roles and functions of γδ T cells in CVID. We observe a higher frequency of Vδ1+ γδ T cells compared to healthy controls, particularly in older patients. We also find a higher proportion of effector-memory Vδ1+ γδ T cells and a more clonal T cell receptor (TCR) repertoire in CVID. The most significant driver of the Vδ1+ γδ T cell expansion and phenotype in CVID patients is persistent cytomegalovirus (CMV) viremia. These findings provide valuable insights into γδ T cell biology and their contribution to immune defence in CVID.