Abstract

The absence of anti-cytomegalovirus (CMV) immunoglobulin G (IgG) is used to classify pretransplant patients as naïve for CMV infection (CMVneg patients). This study assessed whether pretransplant CMV-specific T-cell immunity exists in CMVneg patients and whether it protects against CMV infection after kidney transplantation. The results show that CMV-specific CD137+IFNγ+CD4+ and CD137+IFNγ+CD8+ memory T cells were present in 46 and 39% of CMVneg patients (n = 28) although at much lower frequencies compared to CMVpos patients (median 0.01 versus 0.58% for CD4+ and 0.05 versus 0.64% for CD8+ T cells) with a less differentiated CD28-expressing phenotype. In line with these data, CMV-specific proliferative CD4+ and CD8+ T cells were observed in CMVneg patients, which significantly correlated with the frequency of CMV-specific T cells. CMV-specific IgG antibody-secreting cells (ASC) could be detected at low frequency in 36% of CMVneg patients (1 versus 45 ASC/105 cells in CMVpos patients). CMVneg patients with pretransplant CMV-specific CD137+IFNγ+CD4+ T cells had a lower risk to develop CMV viremia after transplantation with a CMVpos donor kidney (relative risk: 0.43, P = 0.03). In conclusion, a solitary CMV-specific T-cell response without detectable anti-CMV antibodies is frequent and clinically relevant as it is associated with protection to CMV infection following transplantation with a kidney from a CMVpos donor.

Highlights

  • Kidney transplant (KT) recipients are at increased risk for infections following transplantation, one of the major threats being cytomegalovirus (CMV)

  • Data are scarce as to whether the presence of limited cellular immunity protects from CMV viremia after kidney transplantation and no detailed insights into which T-cell subsets are involved in justsufficient protection are available, as cellular immunity is mainly assessed by ELISpot [11]

  • We evaluated the presence of CMV-specific cellular and humoral immunity in a cohort of CMV-seronegative patients and assessed the clinical relevance with respect to the risk for a CMV viremia after kidney transplantation

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Summary

Introduction

Kidney transplant (KT) recipients are at increased risk for infections following transplantation, one of the major threats being cytomegalovirus (CMV). Patients at increased risk for an infection with CMV either receive prophylactic or preemptive antiviral therapy (valganciclovir) following kidney transplantation [2]. Several groups have proposed to include an evaluation of cellular immunity against CMV in the risk assessment strategy to more accurately assess sensitization before transplantation [8,9,10]. Data are scarce as to whether the presence of limited cellular immunity protects from CMV viremia after kidney transplantation and no detailed insights into which T-cell subsets are involved in justsufficient protection are available, as cellular immunity is mainly assessed by ELISpot [11]

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