[Early intervention of BK virus replication promotes stabilization of renal graft function]

Nan Fang Yi Ke Da Xue Xue Bao. 2017 Aug 20;37(8):1110-1115. doi: 10.3969/j.issn.1673-4254.2017.08.18.
[Article in Chinese]

Abstract

Objective: To investigate the optimal time window for intervention of BK virus (BKV) replication and its effect on the outcomes of kidney transplant recipients (KTRs).

Methods: A retrospective analysis of the clinical data and treatment regimens was conducted among KTRs whose urine BKV load was ≥1.0×104 copies/mL following the operation between April, 2000 and April, 2015. KTRs with urine BKV load <1.0×104 copies/mL matched for transplantation time served as the control group.

Results: A total of 54 recipients positive for urine BKV were included in the analysis. According to urine BKV load, the recipients were divided into 3 groups: group A with urine BKV load of 1.0×104-1.0×107 copies/mL (n=22), group B with urine BKV load >1.0×107 copies/mL (n=24), and group C with plasma BKV load ≥1.0×104 copies/mL (n=8); 47 recipients were included in the control group. During the follow-up for 3.2-34.5 months, the urine and plasma BKV load was obviously lowered after intervention in all the 54 BKV-positive recipients (P<0.05). Eighteen (81.82%) of the recipients in group A and 19 (79.17%) in group B showed stable or improved estimated glomerular filtration rate (eGFR) after the intervention; in group C, 4 recipients (50%) showed stable eGFR after the intervention. In the last follow-up, the recipients in groups A and B showed similar eGFR with the control group (P>0.05), but in group C, eGFR was significantly lower than that of the control group (P=0.001). The recipients in group A and the control group had the best allograft outcome with stable or improved eGFR.

Conclusion: Early intervention of BKV replication (urine BKV load ≥1.0×104 copies/mL) in KTRs with appropriate immunosuppression reduction can be helpful for stabilizing the allograft function and improving the long-term outcomes.

目的: 探讨肾移植受者术后BK病毒(BKV)复制的干预时机及转归。

方法: 回顾性分析2012年4月~2015年4月在我院检测尿液BKV载量≥1.0×104/mL肾移植受者的临床资料,选择47例同期接受移植且尿液或血液BKV载量<1.0×104/mL肾移植受者作为对照。

结果: 最终入组实验组54例:A组(尿BKV载量1.0×104~1.0×107/mL)22例,B组(尿BKV载量>1.0×107/mL)24例,C组(血BKV载量≥1.0×104/mL)8例; 对照组47例。经3.2~34.5个月的随访,实验组在干预后尿液、血浆BKV载量均明显降低(P值均<0.05)。进一步比较干预前后估算肾小球滤过率(eGFR)水平,A组:18例(81.82%)eGFR稳定或好转,4例(18.18%)eGFR降低; B组:19例(79.17%)eGFR稳定或好转,5例(20.83%)eGFR降低; C组:4例(50%)eGFR稳定,4例(50%)eGFR降低。截止至末次随访,A组、B组的平均eGFR与对照组比较均无统计学差异(P值均≥0.05),C组的平均eGFR较对照组明显降低(P=0.001)。依各组移植肾eGFR变化趋势显示:干预后A组以及对照组随访期间移植效果最好,eGFR稳定,略呈上升状态。

结论: 在BKV复制早期(尿液BKV≥1.0×104/mL)就予以干预,进行适度的免疫抑制剂减量,有利于稳定移植肾功能,改善移植肾长期存活。

Publication types

  • English Abstract

Grants and funding

国家自然科学基金(81500573); 南方医科大学南方医院院长基金项目(2013B011); 南方医科大学南方医院院级教育课题(14NJ-ZL01); 南方医科大学大学生创新创业训练项目基金(201612121006)