Research and Development, ITB-Med AB, 113 66 Stockholm, Sweden.
Division of Transplantation Surgery, CLINTEC, Karolinska Institute, 141 86 Stockholm, Sweden.
Int J Mol Sci. 2021 Feb 24;22(5):2253. doi: 10.3390/ijms22052253.
Liver transplant (LT) recipients require life-long immunosuppression (IS) therapy to preserve allograft function. The risks of chronic IS include an increased frequency of malignancy, infection, renal impairment, and other systemic toxicities. Despite advances in IS, long-term LT outcomes have not been improved over the past three decades. Standard-of-care (SoC) therapy can, in rare cases, lead to development of operational tolerance that permits safe withdrawal of maintenance IS. However, successful IS withdrawal cannot be reliably predicted and, in current prospective studies, is attempted several years after the transplant procedure, after considerable exposure to the cumulative burden of maintenance therapy. A recent pilot clinical trial in liver tolerance induction demonstrated that peri-transplant immunomodulation, using a regulatory T-cell (Treg) approach, can reduce donor-specific alloreactivity and allow early IS withdrawal. Herein we review protocols for active tolerance induction in liver transplantation, with a focus on identifying tolerogenic cell populations, as well as barriers to tolerance. In addition, we propose the use of novel IS agents to promote immunomodulatory mechanisms favoring tolerance. With numerous IS withdrawal trials underway, improved monitoring and use of novel immunomodulatory strategies will help provide the necessary knowledge to establish an active liver tolerance induction protocol for widespread use.
肝移植 (LT) 受者需要终身接受免疫抑制 (IS) 治疗以维持移植物功能。慢性 IS 的风险包括恶性肿瘤、感染、肾功能损害和其他全身毒性的发生率增加。尽管 IS 取得了进展,但过去三十年来,LT 的长期预后并未得到改善。标准治疗 (SoC) 有时可导致产生允许安全停用维持性 IS 的操作性耐受,但不能可靠预测成功的 IS 停药,而且在当前的前瞻性研究中,在移植手术后数年、在长期接受累积维持治疗负担后才尝试停药。最近在诱导肝耐受的一项试点临床试验中,使用调节性 T 细胞 (Treg) 方法进行移植前免疫调节,可以降低供体特异性同种反应性,并允许早期 IS 停药。本文回顾了 LT 中主动耐受诱导的方案,重点是确定耐受原性细胞群以及耐受的障碍。此外,我们建议使用新型 IS 药物来促进有利于耐受的免疫调节机制。随着许多 IS 停药试验的进行,改进监测和使用新型免疫调节策略将有助于提供建立广泛应用的主动肝耐受诱导方案所需的知识。