Cellular immunity against cytomegalovirus and risk of infection after kidney transplantation

Front Immunol. 2024 Jun 28:15:1414830. doi: 10.3389/fimmu.2024.1414830. eCollection 2024.

Abstract

Introduction: Cytomegalovirus (CMV) infection remains a challenge following kidney transplantation (KTx). Currently, CMV-IgG serostatus at transplantation is used to individualize CMV preventive strategies. We assessed the clinical utility of CMV-IGRA for predicting CMV infection following KTx.

Methods: We performed a nationwide prospective cohort study from August 2016 until December 2022. Data from all adult KTx recipients in Norway, n=1,546 (R+; n=1,157, D+/R-; n=260, D-/R-; 129), were included with a total of 3,556 CMV-IGRA analyses (1,375 at KTx, 1,188 at eight weeks, 993 one-year after KTx) and 35,782 CMV DNAemia analyses.

Results: In R+ recipients CMV-IGRA status, measured at any of the time-points, could not identify any differential risk of later CMV infection. D+/R- recipients remaining CMV-IGRA negative 1-year after transplantation (regardless of positive CMV DNAemia and/or CMV IgG status at that time) had increased risk of developing later CMV infection compared to D+/R- recipients who had become CMV-IGRA positive (14% vs. 2%, p=0.01).

Conclusion: Knowledge of pre-transplant CMV-IGRA status did not provide additional information to CMV-IgG serostatus that could improve current post-transplant CMV treatment algorithms. However, D+/R- recipients with a persisting negative CMV-IGRA one-year after transplantation remained at increased risk of experiencing later CMV infection. Therefore we advocate post-transplant CMV-IGRA monitoring in these patients.

Keywords: CMI (cell mediated immunity); CMV-IGRA; cytomegalovirus (CMV); cytomegalovirus infection; kidney transplansplantation.

MeSH terms

  • Adult
  • Aged
  • Antibodies, Viral / blood
  • Cytomegalovirus Infections* / immunology
  • Cytomegalovirus* / immunology
  • Female
  • Humans
  • Immunity, Cellular*
  • Immunoglobulin G / blood
  • Kidney Transplantation* / adverse effects
  • Male
  • Middle Aged
  • Norway / epidemiology
  • Prospective Studies
  • Risk Factors

Substances

  • Antibodies, Viral
  • Immunoglobulin G

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.