Division of Nephrology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Department of Pharmacy, University of Wisconsin Hospital and Clinics, Madison, WI, USA.
Transpl Infect Dis. 2020 Jun;22(3):e13272. doi: 10.1111/tid.13272. Epub 2020 Mar 16.
Published literature on predictors of polyomavirus (BKV) and cytomegalovirus (CMV) infections in simultaneous pancreas and kidney (SPK) transplant and their impact on allograft outcomes remain sparse. We hypothesize that BKV and CMV viremia infections decrease allograft survival in SPK. Identifying modifiable predictors of BKV and CMV may help tailor immunosuppression and improve allograft survival.
All SPK recipients at our institution between January 2000 and April 2016 were included (n = 757). Thirty-nine recipients had BKV only and 25 had CMV only, and infection occurred at median follow-up times of 217 and 163 days, respectively. Event density sampling was used to match recipients with BKV or CMV to up to 10 recipients without infection by age, sex, and HLA mismatch status, and these were followed for a median of 4.3 years after infection.
Older age (HR 1.49 for each decade; 95% CI: 0.95, 2.35; P = .083) and tacrolimus use (HR 20.6; 95% CI: 2.37, 179.53; P = .006) were associated with increased incidence of BKV, but not CMV, infection. Both BKV and CMV infections were associated with increased risk of allograft failure for both pancreas (BKV [HR 2.17; 95% CI 1.47, 3.208; P = .000], CMV [HR 1.7; 95% CI 1.077, 2.687; P = .023]) and kidney (BKV [HR 2.65; 95% CI 1.765, 3.984; P = .000], CMV [HR 2.07; 95% CI 1.295, 3.308; P = .002]).
Older age at time of transplant and tacrolimus may help predict BKV infection in SPK recipients.
关于同时胰腺和肾脏(SPK)移植中预测多瘤病毒(BK)和巨细胞病毒(CMV)感染及其对移植物结局影响的文献仍然很少。我们假设 BK 和 CMV 病毒血症感染会降低 SPK 的移植物存活率。确定 BK 和 CMV 的可调节预测因子可能有助于调整免疫抑制并改善移植物存活率。
本研究纳入了 2000 年 1 月至 2016 年 4 月期间在我院接受 SPK 的所有受者(n=757)。39 例受者仅发生 BK 感染,25 例仅发生 CMV 感染,感染分别发生在中位随访时间 217 天和 163 天。采用事件密度抽样法,将 BK 或 CMV 感染的受者与多达 10 例未感染的受者进行年龄、性别和 HLA 错配状态匹配,在感染后中位随访 4.3 年后进行随访。
年龄较大(每十年增加 1.49 倍;95%CI:0.95,2.35;P=0.083)和使用他克莫司(HR 20.6;95%CI:2.37,179.53;P=0.006)与 BK 感染发生率增加相关,但与 CMV 感染无关。BK 和 CMV 感染均与胰腺(BK [HR 2.17;95%CI 1.47,3.208;P=0.000]和肾(BK [HR 2.65;95%CI 1.765,3.984;P=0.000])和 CMV 感染相关)移植物失败的风险增加。
移植时年龄较大和使用他克莫司可能有助于预测 SPK 受者的 BK 感染。