Wolner Laurenz, William-Olsson Johan, Podesser Bruno K, Zuckermann Andreas, Pilat Nina
Center for Biomedical Research and Translational Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Department of Cardiac and Thoracic Aortic Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Int J Mol Sci. 2025 Apr 23;26(9):3968. doi: 10.3390/ijms26093968.
Heart transplantation remains the gold-standard treatment for end-stage heart failure, yet long-term graft survival is hindered by chronic rejection and the morbidity and mortality caused by lifelong immunosuppression. While advances in medical and device-based therapies have reduced the overall need for transplantation, patients who ultimately require a transplant often present with more advanced disease and comorbidities. Recent advances in tolerance-inducing strategies offer promising avenues to improve allograft acceptance, while minimizing immunosuppressive toxicity. This review explores novel approaches aiming to achieve long-term immunological tolerance, including co-stimulation blockade, mixed chimerism, regulatory T-cell (Treg) therapies, thymic transplantation, and double-organ transplantation. These strategies seek to promote donor-specific unresponsiveness and mitigate chronic rejection. Additionally, expanding the donor pool remains a critical challenge in addressing organ shortages. Innovations such as ABO-incompatible heart transplantation are revolutionizing the field by increasing donor availability and accessibility. In this article, we discuss the mechanistic basis, clinical advancements, and challenges of these approaches, highlighting their potential to transform the future of heart transplantation with emphasis on clinical translation.
心脏移植仍然是终末期心力衰竭的金标准治疗方法,但长期移植物存活受到慢性排斥反应以及终身免疫抑制所导致的发病率和死亡率的阻碍。虽然基于药物和器械的治疗进展减少了总体移植需求,但最终需要移植的患者往往病情更严重且伴有更多合并症。诱导耐受策略的最新进展为提高同种异体移植物的接受度提供了有前景的途径,同时将免疫抑制毒性降至最低。本综述探讨了旨在实现长期免疫耐受的新方法,包括共刺激阻断、混合嵌合体、调节性T细胞(Treg)疗法、胸腺移植和双器官移植。这些策略旨在促进供体特异性无反应性并减轻慢性排斥反应。此外,扩大供体库仍然是解决器官短缺问题的关键挑战。诸如ABO血型不相容心脏移植等创新正在通过增加供体的可用性和可及性来彻底改变该领域。在本文中,我们讨论了这些方法的机制基础、临床进展和挑战,强调它们在临床转化方面改变心脏移植未来的潜力。