Department of Hepatic Surgery and Liver Transplantation Center of the Third Affiliated Hospital, Organ Transplantation Institute, Sun Yat-sen University, Guangzhou, 510630, Guangdong, China.
Organ Transplantation Research Center of Guangdong Province, Guangzhou, 510630, China.
Stem Cell Res Ther. 2021 Apr 16;12(1):244. doi: 10.1186/s13287-021-02246-4.
ABO-incompatible liver transplantation (ABO-i LT) has become a rescue therapeutic option for patients with severe hepatic failure. Although the use of rituximab greatly reduces the morbidity of antibody-mediated rejection (AMR), severe adverse effects, such as infection and biliary complications, still seriously threaten the survival of transplant recipients. The aim of this study was to evaluate the safety and feasibility of using mesenchymal stem cells (MSCs) to replace rituximab in ABO-i LT.
Twenty-two patients with severe hepatic failure undergoing ABO-i LT were enrolled and randomly divided into two groups: the MSC group and the rituximab group. The safety of the application of MSCs and the incidence of allograft rejection, including antibody-mediated rejection (AMR) and acute cellular rejection (ACR), were evaluated in both groups at the 2-year follow-up period as primary endpoints. Recipients and graft survival and other postoperative complications were compared as secondary endpoints.
No severe MSC-related adverse events were observed during the trial. MSC treatment yielded comparable, if not better, results than rituximab at decreasing the incidence of acute rejection (9.1% vs 27.3%). Inspiringly, compared to those in the rituximab group, the rates of biliary complications (0% vs 45.5%) and infection (9.1% vs 81.8%) were significantly decreased in the MSC group. In addition, there were no significant differences in 2-year graft and recipient survival between the two groups (81.8% vs 72.7%).
Our data show that MSC transfusion is comparable to rituximab treatment for AMR prophylaxis following ABO-i LT. Additionally, the results indicate that MSCs are more beneficial to the prevention of infection and biliary complications and may be introduced as a novel immunosuppressive approach for ABO-i LT.
Trial registration: chictr.org.cn , ChiCTR2000037732. Registered 31 August 2020- Retrospectively registered, http://www.chictr.org.cn/showproj.aspx?proj=57074 .
ABO 不相容肝移植(ABO-i LT)已成为严重肝衰竭患者的一种抢救治疗选择。尽管利妥昔单抗的使用大大降低了抗体介导的排斥反应(AMR)的发病率,但严重的不良反应,如感染和胆道并发症,仍然严重威胁着移植受者的生存。本研究旨在评估间充质干细胞(MSCs)替代 ABO-i LT 中利妥昔单抗的安全性和可行性。
纳入 22 例接受 ABO-i LT 的严重肝衰竭患者,并随机分为两组:MSC 组和利妥昔单抗组。在 2 年的随访期内,评估两组应用 MSCs 的安全性和同种异体移植物排斥反应的发生率,包括抗体介导的排斥反应(AMR)和急性细胞排斥反应(ACR),作为主要终点。比较受者和移植物存活率及其他术后并发症作为次要终点。
在试验过程中未观察到严重的 MSC 相关不良事件。MSC 治疗在降低急性排斥反应的发生率方面与利妥昔单抗相当(9.1% vs 27.3%),如果不是更好的话。令人鼓舞的是,与利妥昔单抗组相比,MSC 组的胆道并发症发生率(0% vs 45.5%)和感染率(9.1% vs 81.8%)显著降低。此外,两组 2 年移植物和受者存活率无显著差异(81.8% vs 72.7%)。
我们的数据表明,MSC 输注与 ABO-i LT 后 AMR 预防的利妥昔单抗治疗相当。此外,结果表明 MSCs 更有利于预防感染和胆道并发症,并且可能作为 ABO-i LT 的一种新的免疫抑制方法引入。
临床试验注册中心,ChiCTR2000037732。注册日期:2020 年 8 月 31 日-回顾性注册,http://www.chictr.org.cn/showproj.aspx?proj=57074。