Long-term CMV monitoring and chronic rejection in renal transplant recipients
- PMID: 37384223
- PMCID: PMC10294236
- DOI: 10.3389/fcimb.2023.1190794
Long-term CMV monitoring and chronic rejection in renal transplant recipients
Abstract
Introduction: Cytomegalovirus (CMV) is well established to be an independent risk factor for graft loss after kidney transplantation (KTx). Monitoring for CMV in the chronic phase is not defined in the current guideline. The effects of CMV infection, including asymptomatic CMV viremia, in the chronic phase are unclear.
Methods: We performed a single-center retrospective study to investigate incidence of CMV infection in the chronic phase, defined as more than 1 year after KTx. We included 205 patients who received KTx between April 2004 and December 2017. The CMV pp65 antigenemia assays to detect CMV viremia were continuously performed every 1-3 months.
Results: The median duration of the follow-up was 80.6 (13.1-172.1) months. Asymptomatic CMV infection and CMV disease were observed in 30.7% and 2.9% in the chronic phase, respectively. We found that 10-20% of patients had CMV infections in each year after KTx which did not change over 10 years. The history of CMV infection in the early phase (within 1 year after KTx) and chronic rejection were significantly associated with CMV viremia in the chronic phase. CMV viremia in the chronic phase was significantly associated with graft loss.
Discussion: This is the first study to examine the incidence of CMV viremia for 10 years post KTx. Preventing latent CMV infection may decrease chronic rejection and graft loss after KTx.
Keywords: CMV; chronic rejection; kidney transplantation; long-term; monitoring.
Copyright © 2023 Ishikawa, Tasaki, Saito, Nakagawa, Ikeda, Takahashi and Tomita.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures
Similar articles
-
Acquisition of Antibody Against Cytomegalovirus After Kidney Transplantation in Seronegative Recipients.Transplant Proc. 2023 May;55(4):809-814. doi: 10.1016/j.transproceed.2023.03.007. Epub 2023 Apr 14. Transplant Proc. 2023. PMID: 37061354
-
Cytomegalovirus-related disease and risk of acute rejection in renal transplant recipients: a cohort study with case-control analyses.Transpl Int. 2000;13(6):413-9. doi: 10.1007/s001470050723. Transpl Int. 2000. PMID: 11140239
-
Kidney function of Japanese children undergoing kidney transplant with preemptive therapy for cytomegalovirus infection.Transpl Infect Dis. 2020 Jun;22(3):e13271. doi: 10.1111/tid.13271. Epub 2020 Mar 11. Transpl Infect Dis. 2020. PMID: 32108410
-
Effect of cytomegalovirus viremia on subclinical rejection or interstitial fibrosis and tubular atrophy in protocol biopsy at 3 months in renal allograft recipients managed by preemptive therapy or antiviral prophylaxis.Transplantation. 2009 Feb 15;87(3):436-44. doi: 10.1097/TP.0b013e318192ded5. Transplantation. 2009. PMID: 19202451
-
Cytomegalovirus infection and graft rejection in renal transplantation.Transplantation. 2001 Mar 27;71(6):764-7. doi: 10.1097/00007890-200103270-00013. Transplantation. 2001. PMID: 11330539
Cited by
-
Virus-specific Th17 Cells Are Induced by Human Cytomegalovirus after Renal Transplantation.J Immunol. 2024 Dec 1;213(11):1703-1712. doi: 10.4049/jimmunol.2300742. J Immunol. 2024. PMID: 39423238
References
-
- Abate D., Fiscon M., Saldan A., Cofano S., Mengoli C., Sgarabotto D., et al. . (2012). Human cytomegalovirus-specific T-cell immune reconstitution in preemptively treated heart transplant recipients identifies subjects at critical risk for infection. J. Clin. Microbiol. 50, 1974. doi: 10.1128/JCM.06406-11 - DOI - PMC - PubMed
-
- Abate D., Saldan A., Fiscon M., Cofano S., Paciolla A., Furian L., et al. . (2010). Evaluation of cytomegalovirus (CMV)-specific T cell immune reconstitution revealed that baseline antiviral immunity, prophylaxis, or preemptive therapy but not antithymocyte globulin treatment contribute to CMV-specific T cell reconstitution in kidney transplant recipients. J. Infect. Dis. 202, 585. doi: 10.1086/654931 - DOI - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous