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Risk Factors of Post-Transplant High-Grade CMV Reactivation in CMV-Seropositive Patients in the Modern Immunosuppressive Era

M. Saito, S. Satoh, K. Numakura, T. Inoue, H. Tsuruta, S. Akihama, N. Tsuchiya, T. Habuchi

Urology, Akita University Graduate School of Medicine, Akita, Japan

Meeting: 2013 American Transplant Congress

Abstract number: 511

Backgrounds: Cytomegalovirus (CMV) prophylaxis is recommended for CMV-seronegative kidney transplant recipients (R-) receiving the grafts from CMV seropositive donors (D+). Meanwhile, whether R+ patients need universal CMV prophylaxis remains undefined. Most of R+ patients with low-grade CMV reactivation show spontaneous remission without deteriorating the graft function and survival. In addition, valganciclovir (VGCV) possibly causes some adverse effects and GCV-resistant CMV. Although targeting CMV prophylaxis to R+ patients is ideal, there are few reports addressing the risk factors of high-grade CMV reactivation in R+ patients in the modern immunosuppressive era.

Methods: Since July 2004, 137 R+ patients who received the kidney from D+ in our hospital were enrolled in this study. No recipients received CMV prophylaxis. The induction immunosuppressive therapy was consisted of tacrolimus, MMF, steroid, and basiliximab. Patients with immunological high risks received a single-low dose of rituximab and 3 to 4 sessions of apheresis prior to transplantation. High-grade CMV reactivation was defined as CMV-antigenemia (Ag) positive cells becoming higher than 10/200,000 blood leukocytes during the clinical course. The CMV-Ag level was monitored at 2 to 3-weekly intervals until 6 months, and at monthly intervals from 6 to 12 months post-transplantation. We investigated the predictive risk factors of high-grade CMV reactivation in R+ patients.

Results: The rate of high-grade CMV reactivation was 25% (34/137) in this series. All patients who developed CMV reactivation were cured by VGCV or GCV successfully without causing GCV-resistant CMV. The graft survival was significantly shorter in the R+ patients with CMV reactivation than those without (p=0.014). In multivariate analysis, the pre-transplant low-IgG titer against CMV (p=0.010) and immunological high risks (p=0.028) were independently associated with the development of high-grade CMV reactivation.

Conclusion: The development of high-grade CMV reactivation deteriorated the graft survival in R+ patients in the modern immunosuppressive era. Pre-transplant low-IgG titer against CMV and immunological high risks were predictive risk factors for the development of high-grade CMV reactivation. To avoid the high-grade CMV reactivation, targeting CMV prophylaxis may be needed for R+ patients with risk factors as stated above.

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To cite this abstract in AMA style:

Saito M, Satoh S, Numakura K, Inoue T, Tsuruta H, Akihama S, Tsuchiya N, Habuchi T. Risk Factors of Post-Transplant High-Grade CMV Reactivation in CMV-Seropositive Patients in the Modern Immunosuppressive Era [abstract]. Am J Transplant. 2013; 13 (suppl 5). https://atcmeetingabstracts.com/abstract/risk-factors-of-post-transplant-high-grade-cmv-reactivation-in-cmv-seropositive-patients-in-the-modern-immunosuppressive-era/. Accessed May 17, 2025.

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