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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Feasibility of Monotherapy by Rituximab Without Additional Desensitization in ABO-incompatible Living-Donor Liver Transplantation
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Feasibility of Monotherapy by Rituximab Without Additional Desensitization in ABO-incompatible Living-Donor Liver Transplantation

机译:Rituximab的单药治疗的可行性,无需额外的脱敏,在ABO-Indompative Lover肝移植中

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摘要

Background. Rituximab is a cornerstone in the regimens of desensitization for ABO-incompatible living-donor liver transplantation (ABO-i LDLT) that makes this modality an acceptable option for liver transplantation. Plasmapheresis (PP) to reduce anti-ABO antibody titer and local infusion (LI) therapy were practiced as the strategies for desensitization before the application of rituximab and were reported as additional treatments. The aim of this study was to clarify the feasibility of monotherapy by rituximab without any additional desensitization treatments in ABO-i LT. Methods. Forty patients receiving ABO-i LDLT with rituximab were enrolled in this retrospective study. The patients were divided into 2 groups: the rituximab with pretransplant PP and posttransplant LI (RPL) group (n = 20) and the rituximab monotherapy (RM) without any additional treatment group (n = 20). The groups were then compared in terms of the rates of patient survival, antibody-mediated rejection (AMR), and infection. Results. The 1-, 3-, and 5-year patient survival rates were 85%, 85%, and 85% in the RPL group and 89%, 80%, and 80% in the RM group, respectively. There was no significant difference in patient survival between the 2 groups. There were no episodes of AMR in either group. The RM group had a lower rate of fungal and viral infections than the RPL group. Conclusions. Pretransplant rituximab without additional treatments yielded satisfactory outcomes comparable to that with additional treatments, such as PP and LI.
机译:背景。 Rituximab是Abo-Indomative Lover肝移植(ABO-I LDLT)的脱敏方案中的基石,使这种模型是肝移植的可接受的选择。降低抗ABO抗体滴度和局部输注(LI)治疗的血浆粉刺(PP)作为拟妥昔单抗施用前的抗敏化策略,并被报告为另外的处理。本研究的目的是阐明RITUXIMAB的单药治疗的可行性,而无需在ABO-1中没有任何额外的脱敏处理。方法。在这个回顾性研究中注册了接受ABO-I LDLT的四十名患者。将患者分为2组:具有预体PP和后翻蛋白Li(RPL)基团(n = 20)的Rituximab和Rituximab单疗法(RM),没有任何额外的处理基团(n = 20)。然后在患者存活率,抗体介导的排斥(AMR)和感染方面进行比较这些组。结果。在RPL组的1-,3-和5年患者存活率分别为85%,85%和85%,分别在RM组中89%,80%和80%。 2组之间的患者存活率没有显着差异。任何一组中都没有AMR剧集。 RM组比RPL组的真菌和病毒感染率较低。结论。预防性治疗的预防性rituximab不与附加治疗相当的令人满意的结果,例如pp和li。

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