Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; Department of Cardiovascular Surgery, University Hospital of Johannes Gutenberg University, Mainz, Germany.
Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
J Heart Lung Transplant. 2022 Aug;41(8):1014-1022. doi: 10.1016/j.healun.2022.04.010. Epub 2022 May 13.
The recent pig heart transplant in a patient at the University of Maryland Medical Center has stimulated renewed interest in the xenotransplantation of organs from genetically engineered pigs. The barriers to the use of pigs as sources of organs have largely been overcome by 2 approaches - (1) the deletion of expression of the three known pig carbohydrate xenoantigens against which humans have preformed antibodies, and (2) the transgenic introduction of human 'protective' proteins, such as complement-regulatory proteins. These gene modifications, coupled with immunosuppressive therapy based on blockade of the CD40/CD154 costimulation pathway, have resulted in survival of baboons with life-supporting pig heart grafts for almost 9 months. The initial clinical success at the University of Maryland reinforces encouraging preclinical results. It suggests that pig hearts are likely to provide an effective bridge to an allotransplant, but their utility for destination therapy remains uncertain. Because of additional complex immunobiological problems, the same approach has been less successful in preclinical lung xenograft transplantation, where survival is still measured in days or weeks. The first formal clinical trials of pig heart transplantation may include patients who do not have access to an allotransplant, those with contraindications for mechanical circulatory support, those in need of retransplantation or with a high level of panel-reactive antibodies. Infants with complex congenital heart disease, should also be considered.
马里兰大学医学中心最近进行的猪心脏移植手术,激发了人们对基因工程猪异种器官移植的重新关注。通过以下两种方法,猪作为器官来源的障碍已基本得到克服:(1) 消除已知三种猪碳水化合物异种抗原的表达,这些抗原会引起人类预先产生抗体;(2) 转染引入人类“保护性”蛋白,如补体调节蛋白。这些基因修饰,再加上基于阻断 CD40/CD154 共刺激途径的免疫抑制治疗,使携带猪心脏移植物的狒狒的存活率延长到近 9 个月,这些移植物可维持生命。马里兰大学的初步临床成功进一步证实了令人鼓舞的临床前结果。这表明猪心脏可能成为有效的同种异体移植桥接,但它们用于终末期治疗的效果仍不确定。由于免疫生物学方面的复杂问题,相同的方法在临床前肺异种移植中效果较差,在这种情况下,移植物的存活率仍以天或周为单位来衡量。猪心脏移植的首次正式临床试验可能包括那些无法进行同种异体移植的患者、那些对机械循环支持有禁忌症的患者、那些需要再次移植的患者或 panel-reactive 抗体水平较高的患者。患有复杂先天性心脏病的婴儿也应被考虑。