Levitsky Josh, Feng Sandy
Division of Gastroenterology & Hepatology, Northwestern University, Chicago, IL, United States.
Division of Transplant Surgery, University of California at San Francisco, San Francisco, CA, United States.
Hum Immunol. 2018 May;79(5):283-287. doi: 10.1016/j.humimm.2017.10.007. Epub 2017 Oct 18.
While advances in immunosuppressive therapy have lowered the rate of acute rejection following liver transplantation, the consequence has been an increase in morbidity and mortality related to the lifelong need for maintenance immunosuppression. These complications include an increased risk of malignancy, infection, metabolic disorders, and chronic kidney disease, as well as high health care costs associated with these therapies and the required drug monitoring. Given these issues, most clinicians attempt trial and error dose minimization with variable success rates, and there has been significant interest in full drug withdrawal in select patients through research protocols. These strategies would be more successful if immunomodulatory therapies early after transplantation could be developed and if immune activation biomarkers guiding drug tapering were available to personalize these approaches. This review will review the mechanisms of liver transplant tolerance and potential strategies to achieve immunosuppression withdrawal.
虽然免疫抑制疗法的进展降低了肝移植后急性排斥反应的发生率,但其后果是与终身维持免疫抑制需求相关的发病率和死亡率有所增加。这些并发症包括恶性肿瘤、感染、代谢紊乱和慢性肾病风险增加,以及与这些疗法和所需药物监测相关的高昂医疗费用。鉴于这些问题,大多数临床医生尝试通过试错法进行剂量最小化,但成功率各不相同,并且通过研究方案在特定患者中完全停药引起了广泛关注。如果能够开发移植后早期的免疫调节疗法,并且有指导药物减量的免疫激活生物标志物来个性化这些方法,这些策略将会更加成功。本综述将回顾肝移植耐受的机制以及实现免疫抑制撤药的潜在策略。