Leon H. Charney Division of Cardiology, Department of Medicine, NYU Langone Health, New York, New York, USA.
Department of Cardiothoracic Surgery, NYU Langone Health, New York, New York, USA.
Am J Transplant. 2022 Dec;22(12):2951-2960. doi: 10.1111/ajt.17190. Epub 2022 Sep 20.
The long-term safety of heart transplants from hepatitis C viremic (NAT+) donors remains uncertain. We conducted a prospective study of all patients who underwent heart transplantation at our center from January 2018 through August 2020. Routine testing was performed to assess for donor-derived cell-free DNA, acute cellular rejection (ACR), antibody-mediated rejection (AMR), and cardiac allograft vasculopathy (CAV). Allograft dysfunction and mortality were also monitored. Seventy-five NAT- recipients and 32 NAT+ recipients were enrolled in the study. All NAT+ recipients developed viremia detected by PCR, were treated with glecaprevir/pibrentasvir at the time of viremia detection, and cleared the virus by 59 days post-transplant. Patients who underwent NAT testing starting on post-operative day 7 (NAT+ Group 1) had significantly higher viral loads and were viremic for a longer period compared with patients tested on post-operative day 1 (NAT+ Group 2). Through 3.5 years of follow-up, there were no statistically significant differences in timing, severity, or frequency of ACR in NAT+ recipients compared with the NAT- cohort, nor were there differences in noninvasive measures of graft injury, incidence or severity of CAV, graft dysfunction, or mortality. There were five episodes of AMR, all in the NAT- group. There were no statistically significant differences between Group 1 and Group 2 NAT+ cohorts. Overall, these findings underscore the safety of heart transplantation from NAT+ donors.
从丙型肝炎病毒血症(NAT+)供体移植心脏的长期安全性仍不确定。我们对 2018 年 1 月至 2020 年 8 月期间在我们中心接受心脏移植的所有患者进行了前瞻性研究。进行常规检测以评估供体游离 DNA、急性细胞排斥(ACR)、抗体介导的排斥(AMR)和心脏移植物血管病(CAV)。还监测了移植物功能障碍和死亡率。共有 75 名 NAT- 受体和 32 名 NAT+ 受体入组研究。所有 NAT+ 受体均出现通过 PCR 检测到的病毒血症,在病毒血症检测时接受 glecaprevir/pibrentasvir 治疗,并在移植后 59 天清除病毒。术后第 7 天开始进行 NAT 检测的患者(NAT+ 组 1)病毒载量明显更高,病毒血症持续时间也更长,与术后第 1 天进行检测的患者(NAT+ 组 2)相比。在 3.5 年的随访中,与 NAT- 队列相比,NAT+ 受体的 ACR 发生时间、严重程度或频率没有统计学差异,也没有在移植物损伤的无创测量、CAV 的发生率或严重程度、移植物功能障碍或死亡率方面的差异。NAT- 组发生了五例 AMR,均发生在 NAT- 组。NAT+ 组 1 和组 2 之间没有统计学差异。总体而言,这些发现强调了从 NAT+ 供体移植心脏的安全性。