Cytomegalovirus drives Vδ1+ γδ T cell expansion and clonality in common variable immunodeficiency
Samantha Chan, Benjamin Morgan, Michelle K. Yong, Mai B. Margetts, Anthony J. Farchione, Erin C. Lucas, Jack Godsell, Nhi Ai Giang, C Slade, Anouk von Borstel, Vanessa L. Bryant, Lauren J. Howson
Abstract
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.