Cytomegalovirus infection alters phenotypes of different γδ T-cell subsets in renal transplant recipients with long-term stable graft function

J Med Virol. 2017 Aug;89(8):1442-1452. doi: 10.1002/jmv.24784. Epub 2017 Mar 6.

Abstract

Cytomegalovirus (CMV) infection alters the phenotypic profiles of T-cells and NK cells in healthy and immunocompromised individuals. Here, we examined the effects of CMV infection on the phenotype and functions of γδ T-cell subsets in renal transplant recipients (RTR) stable several years after transplantation (n = 80) and healthy controls (n = 72). Differentiation status, function, and expression of HLA-DR, CD57, and LIR-1 on Vδ2- and Vδ2+ γδ T-cells were examined in peripheral blood cells using flow cytometry. Percentages of Vδ2- γδ T-cells were higher in RTR who are CMV-seropositive and correlated with CMV antibody levels. Proportions of Vδ2- γδ T-cells expressing HLA-DR, CD57, or LIR-1 were increased in CMV-seropositive RTR and healthy controls compared to their seronegative counterparts. Additionally, Vδ2- γδ T-cells were skewed towards a terminally differentiated phenotype and most expressed CD8 in individuals who were CMV-seropositive. Increased expression of LIR-1 on terminally differentiated Vδ2- γδ T-cells was associated with CMV seropositivity in RTR and controls. The presence of CMV DNA in 15 RTR was associated with higher frequencies of LIR-1+ Vδ2+ γδ T-cells and increased percentages of terminally differentiated effector memory cells in both γδ T-cell subsets. Our study further characterises the effects of CMV and transplantation on γδ T-cell phenotypes.

Keywords: cytomegalovirus; renal transplantation; γδ T-cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, CD / analysis
  • CD57 Antigens / analysis
  • Cytomegalovirus Infections / immunology*
  • Female
  • Flow Cytometry
  • HLA-DR Antigens / analysis
  • Humans
  • Immunophenotyping
  • Kidney Transplantation*
  • Leukocyte Immunoglobulin-like Receptor B1 / analysis
  • Male
  • Middle Aged
  • T-Lymphocyte Subsets / immunology*
  • Transplant Recipients*
  • Young Adult

Substances

  • Antigens, CD
  • CD57 Antigens
  • HLA-DR Antigens
  • LILRB1 protein, human
  • Leukocyte Immunoglobulin-like Receptor B1