Division of Digestive Diseases, University of Cincinnati, Cincinnati, OH.
Division of Infectious Diseases, Department of Medicine, University of Cincinnati, Cincinnati, OH.
Hepatology. 2018 May;67(5):1673-1682. doi: 10.1002/hep.29704. Epub 2018 Mar 26.
Breakthroughs in hepatitis C virus (HCV) treatment and rising rates of intravenous drug use have led to an increase in the number of organ donors who are HCV antibody-positive but serum nucleic acid test (NAT)-negative. The risk of HCV transmission from the liver grafts of these donors to recipients is unknown. To estimate the incidence of HCV transmission, we prospectively followed 26 consecutive HCV antibody-negative (n = 25) or NAT-negative (n = 1) transplant recipients who received a liver graft from donors who were HCV antibody-positive but serum NAT-negative between March 2016 and March 2017. HCV transmission was considered to have occurred if recipients exhibited a positive HCV PCR test by 3 months following transplantation. Drug overdose was listed as the cause of death in 15 (60%) of the donors. One recipient died 18 days after transplantation from primary graft nonfunction and was excluded. Of the remaining 25 recipients, HCV transmission occurred in 4 (16%), at a median follow-up of 11 months, all from donors who died of drug overdose. Three of these patients were treated with direct-acting antiviral therapy, with two achieving a sustained virologic response and one an end-of-treatment response. One patient with HCV transmission died after a complicated postoperative course and did not receive antiviral therapy.
In this prospective cohort of non-HCV liver recipients receiving grafts from HCV antibody-positive/NAT-negative donors, the incidence of HCV transmission was 16%, with the highest risk conferred by donors who died of drug overdose; given the availability of safe and highly effective antiviral therapies, use of such organs could be considered to expand the donor pool. (Hepatology 2018;67:1673-1682).
突破丙型肝炎病毒 (HCV) 治疗和静脉药物使用的增加导致了 HCV 抗体阳性但血清核酸检测 (NAT) 阴性的器官供体数量增加。这些供体的肝移植物将 HCV 传播给受者的风险尚不清楚。为了估计 HCV 传播的风险,我们前瞻性地随访了 26 例连续 HCV 抗体阴性(n = 25)或 NAT 阴性(n = 1)的 HCV 肝移植受者,他们在 2016 年 3 月至 2017 年 3 月期间接受了 HCV 抗体阳性但血清 NAT 阴性的供体的肝移植物。如果受者在移植后 3 个月内出现 HCV PCR 检测阳性,则认为发生了 HCV 传播。在 15 名(60%)供体中,药物过量被列为死亡原因。1 名受者在移植后 18 天因原发性移植物无功能而死亡,被排除在外。在其余 25 名受者中,4 名(16%)发生 HCV 传播,中位随访时间为 11 个月,均来自因药物过量而死亡的供体。其中 3 名患者接受了直接作用抗病毒治疗,2 名获得持续病毒学应答,1 名获得治疗结束应答。1 名 HCV 传播患者在复杂的术后病程后死亡,未接受抗病毒治疗。
在本前瞻性 HCV 肝移植受者队列中,接受 HCV 抗体阳性/NAT 阴性供体肝移植物的患者中,HCV 传播的发生率为 16%,风险最高的是因药物过量而死亡的供体;鉴于安全有效的抗病毒治疗方法的可用性,考虑使用这些器官可以扩大供体池。