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丙型肝炎病毒血症(NAT+)供体心脏移植受者的急性和慢性排斥反应的长期随访。

Long-term follow-up of acute and chronic rejection in heart transplant recipients from hepatitis C viremic (NAT+) donors.

机构信息

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.

出版信息

Am J Transplant. 2022 Dec;22(12):2951-2960. doi: 10.1111/ajt.17190. Epub 2022 Sep 20.

Abstract

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.

摘要

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。

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