Belga Sara, Wright Robert C, Lee Stephen B, Durand Christine M, Doucette Karen
Department of Medicine, Division of Infectious Diseases, University of British Columbia, Vancouver, British Columbia, Canada.
Immunity & Infection Research Centre, Vancouver Coastal Health Research Institute, Vancouver, British Columbia, Canada.
Transpl Infect Dis. 2025 Jul 22:e70054. doi: 10.1111/tid.70054.
In nonendemic areas, transplantation from donors with hepatitis B virus (HBV) to recipients without HBV (D+/R-) has been proposed to expand the donor pool; however, data are limited. We aimed to evaluate the epidemiology of HBV in thoracic organ donors, assess HBV-related thoracic organ nonuse, and determine the impact of HBV D+/R- in recipient outcomes.
Adult first-time heart and lung transplant recipients with negative hepatitis B surface antigen (HBsAg) and HBV nucleic acid testing (NAT) were identified through the Organ Procurement and Transplantation Network between January 2004 and December 2022. Multivariable Cox regression models were built to assess the relationship of donor HBV status with death and graft failure.
Our final cohort included 64,514 thoracic organ transplant recipients, 53 HBV D+/R- (0.1%) versus 64,461 (99.9%) HBV D-/R-, including 34,547 (53.5%) heart and 29,967 lung (46.5%) transplants. Donors with positive HBsAg or HBV NAT tests represented 0.31% of the donor pool. There were no reported cases of thoracic organ nonuse due to hepatitis, nor were there differences in the rates of HBV-NAT or HBsAg positivity in used versus nonused thoracic organs. In multivariable modeling, HBV D+/R- was not associated with increased hazard of death (adjusted hazard ratio (aHR), 0.80 [95% CI, 0.30-2.13], p = 0.652) or graft failure (aHR, 0.73 [95% CI, 0.27-1.93], p = 0.522) at 1-year.
HBV D+/R- thoracic organ transplantation does not appear to have a deleterious impact on recipient or graft survival. However, more data are needed to determine the long-term risk of donor-derived HBV infection and define the optimal management strategies.
在非乙肝流行地区,有人提议将乙肝病毒(HBV)携带者的器官移植给非 HBV 感染者(D+/R-),以扩大供体库;然而,相关数据有限。我们旨在评估胸科器官供体中 HBV 的流行病学情况,评估与 HBV 相关的胸科器官弃用情况,并确定 D+/R- 移植对受体结局的影响。
通过器官获取与移植网络确定 2004 年 1 月至 2022 年 12 月期间乙肝表面抗原(HBsAg)和 HBV 核酸检测(NAT)均为阴性的成年首次心脏和肺移植受者。构建多变量 Cox 回归模型,以评估供体 HBV 状态与死亡和移植物失败之间的关系。
我们的最终队列包括 64,514 名胸科器官移植受者,53 例 D+/R-(0.1%)与 64,461 例 D-/R-(99.9%),其中包括 34,547 例(53.5%)心脏移植和 29,967 例(46.5%)肺移植。HBsAg 或 HBV NAT 检测呈阳性的供体占供体库的 0.31%。没有因肝炎导致胸科器官弃用的报告病例,已使用与未使用的胸科器官中 HBV-NAT 或 HBsAg 阳性率也没有差异。在多变量模型中,D+/R- 与 1 年时死亡风险增加(调整后风险比(aHR),0.80 [95% CI,0.30 - 2.13],p = 0.652)或移植物失败风险增加(aHR,0.73 [95% CI,0.27 - 1.93],p = 0.522)无关。
D+/R- 胸科器官移植似乎对受体或移植物存活没有有害影响。然而,需要更多数据来确定供体来源的 HBV 感染的长期风险,并确定最佳管理策略。