Multiorgan Transplant Program, London Health Sciences Centre, Western University, London, ON, Canada.
Division of Infectious Diseases, Transplant Infectious Diseases Program, University Health Network, Toronto, ON, Canada.
Clin Transplant. 2021 Jun;35(6):e14285. doi: 10.1111/ctr.14285. Epub 2021 Mar 23.
Renal transplant recipients remain at risk of delayed-onset cytomegalovirus (CMV) infection occurring beyond a complete course of prophylaxis. In this retrospective cohort, all 278 patients who received renal allografts from deceased donors from 2014 to 2016 were followed until September 1, 2019. We determined the effect of early-vs late-onset acute rejection (EAR vs LAR [ie, occurring beyond 12 months after transplantation]) on CMV infection and subsequently long-term allograft outcome. Median (IQR) duration of follow-up was 1186.0 (904.7-1531.2) days. Seventy patients including 49 patients with EAR and 21 with LAR received augmented immunosuppression. In the same interval, 40 patients developed CMV infection (36 patients beyond 90 days after transplantation [90%]). In logistic regression analysis, D+/R- CMV serostatus (OR: 5.5, 95% CI: 2.5-12.2) and LAR (OR: 7.9, 95% CI: 2.8-22.2) significantly increased the risk of CMV infection. In Cox proportional hazard model, delayed-onset CMV infection (HR: 2.51, 95% CI: 1.08-5.86) and LAR (HR: 5.46, 95% CI: 2.26-13.14) significantly increased the risk of allograft loss. Patients with LAR are at risk of late-onset CMV infection. Post-LAR, targeted prophylaxis may reduce the risk of CMV infection and subsequently allograft loss. Further studies are required to demonstrate the effect of targeted prophylaxis following LAR.
肾移植受者在完成预防疗程后仍有发生迟发性巨细胞病毒(CMV)感染的风险。在这项回顾性队列研究中,我们对 2014 年至 2016 年期间接受已故供体肾移植的 278 例患者进行了随访,直至 2019 年 9 月 1 日。我们确定了早期急性排斥反应(EAR)与晚期急性排斥反应(LAR,即发生于移植后 12 个月后)对 CMV 感染和随后的长期移植物结局的影响。中位(IQR)随访时间为 1186.0(904.7-1531.2)天。70 例患者包括 49 例 EAR 患者和 21 例 LAR 患者接受了强化免疫抑制治疗。在同一时间段内,40 例患者发生了 CMV 感染(90 天后移植的患者有 36 例[90%])。在逻辑回归分析中,D+/R- CMV 血清学状态(OR:5.5,95%CI:2.5-12.2)和 LAR(OR:7.9,95%CI:2.8-22.2)显著增加了 CMV 感染的风险。在 Cox 比例风险模型中,迟发性 CMV 感染(HR:2.51,95%CI:1.08-5.86)和 LAR(HR:5.46,95%CI:2.26-13.14)显著增加了移植物丢失的风险。LAR 患者有发生迟发性 CMV 感染的风险。在发生 LAR 后,靶向预防可能会降低 CMV 感染和随后移植物丢失的风险。需要进一步的研究来证明 LAR 后靶向预防的效果。