Department of Medicine, Division of Cardiology, Columbia University Irving Medical Center, Columbia University, New York, NY, United States.
Front Immunol. 2021 Aug 24;12:702186. doi: 10.3389/fimmu.2021.702186. eCollection 2021.
Heart transplant candidates sensitized to HLA antigens wait longer for transplant, are at increased risk of dying while waiting, and may not be listed at all. The increasing prevalence of HLA sensitization and limitations of current desensitization strategies underscore the urgent need for a more effective approach. In addition to pregnancy, prior transplant, and transfusions, patients with end-stage heart failure are burdened with unique factors placing them at risk for HLA sensitization. These include homograft material used for congenital heart disease repair and left ventricular assist devices (LVADs). Moreover, these risks are often stacked, forming a seemingly insurmountable barrier in some cases. While desensitization protocols are typically implemented uniformly, irrespective of the mode of sensitization, the heterogeneity in success and post-transplant outcomes argues for a more tailored approach. Achieving this will require progress in our understanding of the immunobiology underlying the innate and adaptive immune response to these varied allosensitizing exposures. Further attention to B cell activation, memory, and plasma cell differentiation is required to establish methods that durably abrogate the anti-HLA antibody response before and after transplant. The contribution of non-HLA antibodies to the net state of sensitization and the potential implications for graft longevity also remain to be comprehensively defined. The aim of this review is to first bring forth select issues unique to the sensitized heart transplant candidate. The current literature on desensitization in heart transplantation will then be summarized providing context within the immune response. Building on this, newer approaches with therapeutic potential will be discussed emphasizing the importance of not only addressing the short-term pathogenic consequences of circulating HLA antibodies, but also the need to modulate alloimmune memory.
心脏移植候选者对 HLA 抗原致敏后等待移植的时间更长,等待期间死亡风险增加,甚至可能根本无法被列入名单。HLA 致敏的患病率不断增加,以及当前脱敏策略的局限性,突显了迫切需要更有效的方法。除了妊娠、既往移植和输血外,终末期心力衰竭患者还面临着独特的风险因素,使他们容易致敏。这些因素包括用于先天性心脏病修复的同种异体移植物和左心室辅助装置 (LVAD)。此外,这些风险往往是相互叠加的,在某些情况下形成了看似不可逾越的障碍。虽然脱敏方案通常是统一实施的,而不考虑致敏模式,但在成功和移植后结果方面的异质性表明需要更有针对性的方法。要实现这一目标,需要在我们对固有和适应性免疫对这些不同同种致敏暴露的反应的免疫生物学方面取得进展。进一步关注 B 细胞激活、记忆和浆细胞分化,以建立在移植前后持久消除抗 HLA 抗体反应的方法。非 HLA 抗体对致敏状态的净影响以及对移植物寿命的潜在影响仍有待全面定义。本综述的目的首先是提出针对致敏心脏移植候选者的特有问题。然后将总结心脏移植中脱敏的现有文献,提供免疫反应方面的背景知识。在此基础上,将讨论具有治疗潜力的新方法,强调不仅要解决循环 HLA 抗体的短期致病后果,还需要调节同种免疫记忆。