From the Department of Surgery (B.P.G., C.E.G., A.K.S., C.L.L., A.S., M.M.M.), the Program in Trauma, R. Adams Cowley Shock Trauma Center, Department of Medicine (A.G.), the Institute of Human Virology, Division of Infectious Diseases (K.K.S.), and the Department of Medicine, Division of Cardiology (S.N.H., S.M.J.), University of Maryland School of Medicine, Baltimore, and United Therapeutics, Silver Spring (M.R., M.L.) - both in Maryland; and Revivicor, Blacksburg, VA (D.A.).
N Engl J Med. 2022 Jul 7;387(1):35-44. doi: 10.1056/NEJMoa2201422. Epub 2022 Jun 22.
A 57-year-old man with nonischemic cardiomyopathy who was dependent on venoarterial extracorporeal membrane oxygenation (ECMO) and was not a candidate for standard therapeutics, including a traditional allograft, received a heart from a genetically modified pig source animal that had 10 individual gene edits. Immunosuppression was based on CD40 blockade. The patient was weaned from ECMO, and the xenograft functioned normally without apparent rejection. Sudden diastolic thickening and failure of the xenograft occurred on day 49 after transplantation, and life support was withdrawn on day 60. On autopsy, the xenograft was found to be edematous, having nearly doubled in weight. Histologic examination revealed scattered myocyte necrosis, interstitial edema, and red-cell extravasation, without evidence of microvascular thrombosis - findings that were not consistent with typical rejection. Studies are under way to identify the mechanisms responsible for these changes. (Funded by the University of Maryland Medical Center and School of Medicine.).
一名 57 岁的男子患有非缺血性心肌病,依赖于静脉动脉体外膜肺氧合(ECMO),且不符合包括传统同种异体移植物在内的标准治疗的条件,他接受了一颗来自基因修饰猪源动物的心脏,该心脏经过了 10 项个体基因编辑。免疫抑制基于 CD40 阻断。患者成功脱离 ECMO,异种移植物功能正常,无明显排斥反应。移植后第 49 天,异种移植物出现舒张期增厚和功能衰竭,第 60 天停止生命支持。尸检发现异种移植物水肿,重量几乎增加了一倍。组织学检查显示散在的心肌坏死、间质水肿和红细胞渗出,无微血管血栓形成的证据 - 这些发现与典型排斥反应不一致。目前正在进行研究以确定导致这些变化的机制。(由马里兰大学医学中心和医学院资助)。