PD-1 analysis on CD28(-) CD27(-) CD4 T cells allows stimulation-independent assessment of CMV viremic episodes in transplant recipients

Am J Transplant. 2013 Dec;13(12):3132-41. doi: 10.1111/ajt.12480. Epub 2013 Oct 22.

Abstract

Expression of the inhibitory receptor programmed death 1 (PD-1) on cytomegalovirus (CMV)-specific CD4 T cells defines a phenotype associated with CMV viremia in transplant recipients. Moreover, CD28(-) CD27(-) double negativity is known as a typical phenotype of CMV-specific CD4 T cells. Therefore, the co-expression of inhibitory receptors on CD28(-) CD27(-) CD4 T cells was assessed as a rapid, stimulation-independent parameter for monitoring CMV complications after transplantation. Ninety-three controls, 67 hemodialysis patients and 81 renal transplant recipients were recruited in a cross-sectional and longitudinal manner. CMV-specific CD4 T cell levels quantified after stimulation were compared to levels of CD28(-) CD27(-) CD4 T cells. PD-1 and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) expression on CD28(-) CD27(-) CD4 T cells were related to viremia. A percentage of ≥0.44% CD28(-) CD27(-) CD4 T cells defined CMV seropositivity (93.3% sensitivity, 97.1% specificity), and their frequencies correlated strongly with CMV-specific CD4 T cell levels after stimulation (r = 0.73, p < 0.0001). Highest PD-1 expression levels on CD28(-) CD27(-) CD4 T cells were observed in patients with primary CMV viremia and reactivation (p < 0.0001), whereas CTLA-4 expression was only elevated during primary CMV viremia (p < 0.05). Longitudinal analysis showed a significant increase in PD-1 expression in relation to viremia (p < 0.001), whereas changes in nonviremic patients were nonsignificant. In conclusion, increased PD-1 expression on CD28(-) CD27(-) CD4 T cells correlates with CMV viremia in transplant recipients and may serve as a specific, stimulation-independent parameter to guide duration of antiviral therapy.

Keywords: CD27; CD28; T cell; cytomegalovirus; monitoring; transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / chemistry
  • CD28 Antigens / metabolism*
  • CD4-Positive T-Lymphocytes / cytology*
  • Case-Control Studies
  • Cross-Sectional Studies
  • Cytomegalovirus
  • Cytomegalovirus Infections / complications*
  • Flow Cytometry
  • Humans
  • Kidney Transplantation
  • Middle Aged
  • Phenotype
  • Postoperative Complications
  • Programmed Cell Death 1 Receptor / metabolism*
  • Renal Dialysis
  • Renal Insufficiency / blood*
  • Renal Insufficiency / complications
  • Renal Insufficiency / therapy
  • Sensitivity and Specificity
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / metabolism*
  • Viremia / complications*

Substances

  • Antiviral Agents
  • CD28 Antigens
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Tumor Necrosis Factor Receptor Superfamily, Member 7