静脉注射免疫球蛋白治疗肾移植受者持续性BK病毒血症和BK病毒肾病的疗效

Clinical transplants Pub Date : 2014-01-01
Tariq Shah, Don Vu, Robert Naraghi, Annabelle Campbell, David Min
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摘要

BK病毒相关性肾病(BKVN)可在肾移植受者中引起临床显著的病毒感染,导致同种异体移植物功能障碍和丧失。BKVN的通常治疗包括减少免疫抑制和添加来氟米特、喹诺酮类药物和西多福韦,但移植物损失的比率仍然很高。本研究的目的是评估静脉注射免疫球蛋白(IVIG)治疗对肾移植受者BKVN结局的影响。在诊断为BKVN后,患者继续接受抗多瘤病毒治疗,包括减少免疫抑制和使用来氟米特治疗。IVIG治疗仅适用于对免疫抑制和来氟米特8周调整无效的患者。所有30例患者均有持续性BK病毒血症和BKVN,其平均BK病毒载量高于基线(范围为15,000 - 200万拷贝/mL)。平均峰值BK载量为205,314拷贝/mL,而随访1年后为697拷贝/mL。27例(90%)患者清除病毒血症阳性。12个月后患者和移植物的精算存活率分别为100%和96.7%。IVIG在治疗BK病毒血症和BKVN以及预防对免疫抑制减少和来氟米特治疗反应不足的患者移植物丢失方面似乎是安全有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Intravenous Immunoglobulin in the Treatment of Persistent BK Viremia and BK Virus Nephropathy in Renal Transplant Recipients.

BK virus associated nephropathy (BKVN) can cause clinically significant viral infections in renal transplant recipients, leading to allograft dysfunction and loss. The usual management of BKVN involves reduction of immunosuppression and the addition of leflunomide, quinolones, and cidofovir, but the rate of graft loss remains high. The aim of this study was to assess the impact of treatment with intravenous immunoglobulin (IVIG) on the outcome of BKVN in renal transplant recipients. Upon diagnosis of BKVN, patients remained on anti-polyomavirus treatment consisting of reduction of immunosuppression and the use of leflunomide therapy. Treatment with IVIG was given only to patients who did not respond to 8 weeks of the adjustment of immunosuppression and leflunomide. All 30 patients had persistent BK viremia and BKVN with their mean BK viral loads higher than the baseline (range 15,000 - 2 millions copies/mL). Mean peak BK load was 205,314 copies/mL compared to 697 copies/mL after one year follow-up. Twenty-seven patients (90%) had positive responses in clearing viremia. The actuarial patient and graft survival rates after 12 months were 100% and 96.7%, respectively. IVIG administration appeared to be safe and effective in treating BK viremia and BKVN and in preventing graft loss in patients who had inadequate response to immunosuppression reduction and leflunomide therapy.

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