4.7 Article

A novel MSC-based immune induction strategy for ABO-incompatible liver transplantation: a phase I/II randomized, open-label, controlled trial

期刊

STEM CELL RESEARCH & THERAPY
卷 12, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13287-021-02246-4

关键词

Mesenchymal stem cells; ABO-incompatible liver transplantation; Severe hepatic failure; Rituximab

资金

  1. National Key R&D Program of China [2017YFA0104304]
  2. National Natural Science Foundation of China [81770648, 81802402, 81870449, 81900597, 81970567]
  3. National Key R&D Program of Guangdong Province [2019B020236003]
  4. Guangdong Natural Science Foundation [2017A030311034, 2018A030310323, 2018A030313043, 2018A030313705, 2019A1515011698]
  5. Medical Scientific Research Foundation of Guangdong Province [A2018130]
  6. Sci-tech Research Development Program of Guangzhou city [158100076]
  7. Young Teacher Development Program of Sun Yat-Sen University [17ykpy57, 19ykpy35, 20ykpy41]
  8. China Postdoctoral Science Foundation [2019 M653199]
  9. Academician Shusen Lanjuan Talent foundation

向作者/读者索取更多资源

The study aimed to evaluate the safety and feasibility of using mesenchymal stem cells (MSCs) to replace rituximab in ABO-i LT. Results showed that MSC treatment had comparable, if not better, results at decreasing the incidence of acute rejection, and significantly decreased the rates of biliary complications and infection compared to rituximab. The findings suggest that MSCs may be introduced as a novel immunosuppressive approach for ABO-i LT.
Background: 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. Methods: 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. Results: 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%). Conclusions: 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.

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