Department of Hepatobiliary and Pancreatic Surgery Affiliated Hangzhou First People's HospitalZhejiang University School of Medicine Hangzhou China Division of Hepatobiliary and Pancreatic SurgeryDepartment of Surgery The First Affiliated HospitalZhejiang University School of Medicine Hangzhou China National Health and Family Planning Commission (NHFPC) Key Laboratory of Combined Multi-Organ Transplantation Hangzhou China Department of Hepatobiliary and Pancreatic Surgery Shulan (Hangzhou) Hospital Hangzhou China Department of Surgery University of Cambridge Cambridge UK Cambridge National Institute of Health Research Biomedical Research Centre Cambridge UK.
Liver Transpl. 2021 Feb;27(2):264-280. doi: 10.1002/lt.25948. Epub 2020 Dec 23.
Liver transplantation (LT) is considered the gold standard of curative treatment for patients with end-stage liver disease or nonresectable hepatic malignant tumors. Rejection after LT is the main nontechnical factor affecting the prognosis of recipients. Medical and surgical advances, combined with improved immunosuppression with drugs such as calcineurin inhibitors (CNIs), have contributed to an increase in 1-year graft survival to around 80%. However, medium- and long-term improvements in LT outcomes have lagged behind. Importantly, CNIs and other classical immunosuppressive drugs are associated with significant adverse effects, including malignancies, cardiovascular disease, and severe renal dysfunction. Immunomodulation using regulatory T cells (Tregs) is emerging as a promising alternative to classical immunosuppression. Since their discovery, the immunomodulatory effects of Tregs have been demonstrated in a range of diseases. This has rejuvenated the interest in using Tregs as a therapeutic strategy to induce immune tolerance after LT. In this review, we first summarize the discovery and development of Tregs. We then review the preclinical data supporting their production, mechanism of action, and therapeutic efficacy followed by a summary of relevant clinical trials. Finally, we discuss the outstanding challenges of Treg therapy and its future prospects for routine use in LT.
肝移植(LT)被认为是治疗终末期肝病或不可切除肝恶性肿瘤患者的金标准。LT 后的排斥反应是影响受者预后的主要非技术因素。医学和外科技术的进步,加上钙调神经磷酸酶抑制剂(CNIs)等药物改善免疫抑制作用,使 1 年移植物存活率提高到 80%左右。然而,LT 结果的中、长期改善却落后了。重要的是,CNIs 和其他经典免疫抑制剂会引起严重的不良反应,包括恶性肿瘤、心血管疾病和严重的肾功能障碍。使用调节性 T 细胞(Tregs)进行免疫调节作为经典免疫抑制的替代方法正受到关注。自发现以来,Tregs 的免疫调节作用已在多种疾病中得到证实。这重新激发了人们对使用 Tregs 作为 LT 后诱导免疫耐受的治疗策略的兴趣。在这篇综述中,我们首先总结了 Tregs 的发现和发展。然后,我们回顾了支持 Tregs 产生、作用机制和治疗效果的临床前数据,接着对相关的临床试验进行了总结。最后,我们讨论了 Treg 治疗的突出挑战及其在 LT 中的常规应用的未来前景。