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Long-Term Follow-Up of Active Treatment Versus Minimization of Immunosuppressive Agents in Patients With BK Virus-Associated Nephropathy After Kidney Transplant

机译:肾移植术后BK病毒相关性肾病患者积极治疗的长期随访与免疫抑制剂的降低

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Objectives: There is no active treatment for postrenal transplant BK virus-associated nephropathy proven to be effective so far. We assessed the effectiveness of actively treating this condition with combined leflunomide, intravenous immunoglobulin, and ciprofloxacin on long-term graft outcome compared with minimization of immunosuppressive drugs. Materials and Methods: Kidney transplant re-cipients were screened for BK virus-associated nephropathy. Group 1 comprised 22 kidney trans-plant recipients with twice-positive BK virus polymerase chain reaction results in urine and blood. After diagnosis was confirmed with graft biopsy, antimetabolite (mycophenolate mofetil or aza-thioprine) was changed to leflunomide and intravenous immunoglobulin and oral ciprofloxacin were given. Group 2 comprised 33 BK virus-associated nephro-pathy patients treated conven-tionally with reduced immunosuppressive medications. Results: Fifty-five patients were treated (38 males [69%], 28 patients [50.9%] with type 2 diabetes mellitus). Mean HLA antigen mismatches were 3.65, and 28 patients (50.9%) were HLA-Cw7 negative. All patients received induction therapy, 30 patients (55.6%) received thymoglobulin, and 29 patients (52.7%) received antirejection therapy before BK virus-associated nephropathy diagnosis. Maintenance immunosuppression was prednisolone in 53 patients (96.3%), mycophenolate mofetil (2 g daily) in 52 patients (94.5%), and tacrolimus in 28 patients (50.9%). Subsequent rejection episodes occurred in 38% of patients after diagnosis. Basal mean estimated glomerular filtration rate was 52.5 ± 25.5, which was reduced significantly to 38.1 ± 27.8 mL/min/1.73 m2 ( P < .0001) at end of study but without significant differences between the groups ( P = .08 and P = .17). Follow-up was 7.3 ± 4.99 years. Although no significant differences were shown in patient outcome, graft survival was significantly better in group 2 ( P = .032). Conclusions: Administration of 3 different anti-BK virus agents (leflunomide, intravenous immuno-globulin, ciprofloxacin) added no benefit to long-term outcome in patients with BK virus-associated nephropathy. Reduction of immunosuppressive medications appears to be a more effective treatment.
机译:目的:到目前为止,尚无针对肾移植后BK病毒相关性肾病有效的积极治疗方法。我们评估了将来氟米特,静脉内免疫球蛋白和环丙沙星联合使用可积极治疗此病的长期移植效果,而与最小化免疫抑制药物相比,该方法的有效性。材料与方法:筛选肾移植受者中与BK病毒相关的肾病。第一组包括22位肾脏移植受者,其两次阳性BK病毒聚合酶链反应导致尿液和血液。经移植活检确诊后,将抗代谢药物(霉酚酸酯或氮杂硫代嘌呤)改为来氟米特,并给予静脉免疫球蛋白和口服环丙沙星。第2组包括33例BK病毒相关肾病患者,这些患者常规接受了减少的免疫抑制药物治疗。结果:共治疗了55例患者(男38例[69%],28例25%的患者[50.9%])。平均HLA抗原错配为3.65,HLA-Cw7阴性的28例患者(50.9%)。所有患者均接受了诱导治疗,其中30例(55.6%)接受了胸腺球蛋白,29例患者(52.7%)接受了抗排斥治疗,然后才诊断出BK病毒相关的肾病。维持免疫抑制的患者为53名患者(96.3%)泼尼松龙,霉酚酸酯(每天2 g)52例(94.5%)和他克莫司28例(50.9%)。诊断后38%的患者发生随后的排斥反应。基本平均肾小球滤过率估计为52.5±25.5,在研究结束时显着降低至38.1±27.8 mL / min / 1.73 m2(P <.0001),但两组之间无显着差异(P = .08和P = .17)。随访时间为7.3±4.99年。尽管在患者预后方面没有显着差异,但第2组的移植物存活率显着提高(P = .032)。结论:给予3种不同的抗BK病毒药物(来氟米特,静脉内免疫球蛋白,环丙沙星)对BK病毒相关性肾病患者的长期结局无益。减少免疫抑制药物似乎是一种更有效的治疗方法。

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