Division of Nephrology, Department of Medicine, University of Wisconsin-Madison School of Medicine and Public Health, University of Wisconsin Hospital and Clinics, Madison, WI, USA.
Division of infectious disease, Department of Medicine, University of Wisconsin-Madison School of Medicine and Public Health, University of Wisconsin Hospital and Clinics, Madison, WI, USA.
Transpl Infect Dis. 2020 Aug;22(4):e13317. doi: 10.1111/tid.13317. Epub 2020 May 22.
Minimal data exist describing the epidemiology, management, and long-term graft outcomes after West Nile viral disease in kidney transplant recipients (KTRs).
Single-center observational cohort study of patients who received a kidney transplant between 1/1/1994 and 12/31/2018 and developed WNV at any time point after transplantation.
During the 24-year study period, 11 patients had documented WNV infection. Seven patients were recipients of a kidney transplant alone, and four had a simultaneous kidney and pancreas transplant. The mean age at the time of transplant was 44.7 ± 17.1 years, and the mean age at the time of WNV infection was 48 ± 17.2 years. All patients received lymphocyte depleting induction at transplant (alemtuzumab (n = 2), OKT3 (n = 1), or anti-thymocyte globulin (n = 8)). The mean time from transplant to WNV infection was 3.4 ± 5.4 years, and none was suspected of having a donor-derived infection. Three patients were treated for rejection in the 6 months before infection. The most common presenting symptom was altered mental status (n = 7), followed by a combination of fever and headache (n = 4). All patients had detectable serum WNV IgM antibodies at the time of diagnosis. All patients had a reduction in their immunosuppression and received supportive care; only two patients were treated with intravenous immunoglobulins. Nine patients recovered with no residual deficit; however, two suffered permanent neurologic damage. The mean estimated glomerular filtration rate drop at 1 year after the infection was 8.4 ± 13 mL/min/1.73 m . Three patients suffered acute rejection within 1 year after the infection episode, likely attributable to aggressive immunosuppressive reduction. The mean follow-up after the infection was 5.1 ± 4.3 years. At last follow-up, two patients lost their kidney allograft, and five patients died. None of the graft losses or deaths occurred within a year of the WNV or were directly attributable to WNV.
The majority of patients with WNV infection after KTR recovered fully with supportive care and immunosuppressive adjustment without residual neurologic sequelae. Additionally, WNV infection was associated with relatively small reductions in eGFR at 1 year.
描述肾移植受者(KTR)感染西尼罗河病毒后的流行病学、治疗和长期移植物结局的数据很少。
本研究为单中心观察性队列研究,纳入了 1994 年 1 月 1 日至 2018 年 12 月 31 日期间接受肾移植并在移植后任何时间点发生西尼罗河病毒感染的患者。
在 24 年的研究期间,有 11 名患者确诊为西尼罗河病毒感染。7 名患者为单独接受肾移植,4 名患者同时接受肾和胰腺移植。移植时的平均年龄为 44.7±17.1 岁,西尼罗河病毒感染时的平均年龄为 48±17.2 岁。所有患者在移植时均接受淋巴细胞耗竭诱导(阿仑单抗(n=2)、OKT3(n=1)或抗胸腺细胞球蛋白(n=8))。从移植到西尼罗河病毒感染的平均时间为 3.4±5.4 年,且均未怀疑为供体源性感染。3 名患者在感染前 6 个月因排斥反应接受治疗。最常见的表现症状为精神状态改变(n=7),其次为发热和头痛(n=4)。所有患者在诊断时均检测到血清西尼罗河病毒 IgM 抗体。所有患者均减少免疫抑制并接受支持性治疗;仅 2 名患者接受静脉注射免疫球蛋白治疗。9 名患者康复,无残留缺陷;然而,2 名患者遭受永久性神经损伤。感染后 1 年时估计肾小球滤过率下降的平均值为 8.4±13mL/min/1.73m 。3 名患者在感染后 1 年内发生急性排斥反应,可能归因于免疫抑制药物的大量减少。感染后的平均随访时间为 5.1±4.3 年。最后一次随访时,2 名患者的肾脏移植物丢失,5 名患者死亡。WNV 感染或直接归因于 WNV 导致的移植物丢失或死亡均未在感染后 1 年内发生。
接受肾移植的患者发生西尼罗河病毒感染后,大多数患者通过支持性治疗和免疫抑制调整完全康复,无残留神经后遗症。此外,感染后 1 年时估算的肾小球滤过率有较小幅度的降低。