Medical Services, Ralph H. Johnson VA Medical Center, Charleston, South Carolina, USA.
Department of Medicine, Division of Nephrology, Medical University of South Carolina, Charleston, South Carolina, USA.
Transpl Infect Dis. 2024 Oct;26(5):e14318. doi: 10.1111/tid.14318. Epub 2024 Jun 30.
The goal was to determine trends in immunosuppression use and its impact on cytomegalovirus (CMV) outcomes over the past 10 years.
This was a single-center longitudinal cohort study of adult kidney recipients transplanted between Jan 2012 and June 2021. Baseline and follow-up data were gathered via chart abstraction and analyzed using univariate and multivariate analyses.
Of 2392 kidney transplants conducted, 131 patients did not meet inclusion criteria. The mean age was 52 years, 41% were female, 57% were black, and 19% were CMV high-risk. The use of rabbit anti-thymocyte globulin (RATG) induction (odds ratio [OR] 1.6, 1.3-2.1), tacrolimus (FK) level >8 ng/mL (OR 1.1, 1.09-1.11), CMV D+/R- rates (OR 1.06, 1.02-1.10), white blood cell count <3000 (OR 1.22, 1.18-1.26) and valganciclovir prophylaxis (OR 1.7, 1.6-1.9) have significantly increased over the past 10 years. Rejection rates (OR 0.86, 0.82-0.91) and BK viremia >2000 (OR 0.91, 0.91-0.98) have decreased. RATG induction (adjusted hazard ratio [aHR] 1.35, 1.2-1.5), FK >8 ng/mL (aHR 3.5, 3.2-3.9), Belatacept conversion (aHR 2.5, 2.1-3.1), and rejection (aHR 1.8, 1.6-2.0) were significant risk factors for developing CMV infection, while mycophenolate mofetil <1500 mg (aHR 0.52, 0.47-0.59), mammalian target of rapamycin inhibitor (mTORi) conversion (0.77, 0.56-0.89), cyclosporine-A conversion (aHR 0.68, 0.56-0.84) were associated with lower risk of CMV infection.
Increasing use of potent immunosuppression coupled with higher CMV D+/R- F rates may be driving higher rates of CMV infection. Cyclosporine and mTORi conversion appears to be protective against CMV. A more individualized immunosuppression regimen based on infection risk merits consideration.
本研究旨在确定过去 10 年中免疫抑制药物的使用趋势及其对巨细胞病毒(CMV)结局的影响。
这是一项单中心、回顾性队列研究,纳入 2012 年 1 月至 2021 年 6 月期间接受肾脏移植的成年患者。通过病历摘录收集基线和随访数据,并使用单变量和多变量分析进行分析。
在 2392 例肾脏移植中,有 131 例患者不符合纳入标准。患者的平均年龄为 52 岁,41%为女性,57%为黑人,19%为 CMV 高风险。兔抗胸腺细胞球蛋白(RATG)诱导(比值比[OR] 1.6,1.3-2.1)、他克莫司(FK)水平>8ng/mL(OR 1.1,1.09-1.11)、CMV D+/R-率(OR 1.06,1.02-1.10)、白细胞计数<3000(OR 1.22,1.18-1.26)和缬更昔洛韦预防(OR 1.7,1.6-1.9)在过去 10 年中显著增加。排斥反应率(OR 0.86,0.82-0.91)和 BK 病毒血症>2000(OR 0.91,0.91-0.98)下降。RATG 诱导(调整后的危险比[aHR] 1.35,1.2-1.5)、FK>8ng/mL(aHR 3.5,3.2-3.9)、贝利木单抗转换(aHR 2.5,2.1-3.1)和排斥反应(aHR 1.8,1.6-2.0)是 CMV 感染的显著危险因素,而吗替麦考酚酯<1500mg(aHR 0.52,0.47-0.59)、雷帕霉素靶蛋白抑制剂(mTORi)转换(0.77,0.56-0.89)和环孢素 A 转换(aHR 0.68,0.56-0.84)与 CMV 感染的风险较低相关。
免疫抑制药物使用强度的增加与更高的 CMV D+/R-率可能导致 CMV 感染率增加。环孢素和 mTORi 的转换似乎对 CMV 有保护作用。基于感染风险的个体化免疫抑制方案值得考虑。