Department of Cardiovascular Surgery, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
ASAIO J. 2012 Nov-Dec;58(6):554-61. doi: 10.1097/MAT.0b013e31826d6070.
Left ventricular assist devices (LVADs) have become an established surgical therapy for patients with end-stage heart failure who require hemodynamic support as a bridge-to-transplant or destination therapy. However, the anatomic and physiologic consequences of long-term LVAD support have yet to be fully clarified. Despite the clinical success of these devices, it has been reported that many patients bridged to transplantation with mechanical support develop circulating antibodies with potential donor reactivity. Transplanting against existing or historic donor-specific antibodies is associated with increased risk of antibody-mediated rejection, graft dysfunction, and decreased survival. Safe transplantation of allosensitized patients is dependent on using prospective crossmatching and antibody titer reduction techniques (desensitization). Strict protocols requiring a negative prospective crossmatch before transplantation result in a decreased donor pool and a longer duration of support in sensitized LVAD recipients with increased inherent morbidity such as infections and thromboembolic complications. The aim of this review is to present the current state of knowledge of possible immunologic mechanisms involved in alloimmunization of LVAD recipients, outline new methods of antibody detection, compare various desensitization strategies, and present an overview of clinical data assessing the impact of sensitization on posttransplantation outcome.
左心室辅助装置(LVAD)已成为终末期心力衰竭患者的一种既定手术治疗方法,这些患者需要血液动力学支持作为移植桥或目的地治疗。然而,长期 LVAD 支持的解剖和生理后果尚未完全阐明。尽管这些设备在临床上取得了成功,但据报道,许多接受机械支持桥接移植的患者会产生具有潜在供体反应性的循环抗体。移植与现有或历史供体特异性抗体存在会增加抗体介导排斥反应、移植物功能障碍和降低存活率的风险。同种致敏患者的安全移植取决于使用前瞻性交叉配型和抗体滴度降低技术(脱敏)。在移植前需要进行阴性前瞻性交叉配型的严格方案会导致供体数量减少,并且在感染和血栓栓塞等固有发病率增加的致敏 LVAD 受者中支持时间延长。本综述的目的是介绍 LVAD 受者同种免疫中涉及的可能免疫机制的最新知识,概述新的抗体检测方法,比较各种脱敏策略,并概述评估致敏对移植后结果影响的临床数据。