Assistance Publique-Hôpitaux de Paris AP-HP, Hôpital Universitaire Henri Mondor, Service de Néphrologie et Transplantation, Fédération Hospitalo-Universitaire (Innovative Therapy for Immune Disorders), Créteil, France.
Université Paris Est Créteil UPEC, Institut National de la Santé et de la Recherche Médicale INSERM U955, Institut Mondor de Recherche Biomédicale IMRB, Équipe 21, Créteil, France.
Front Immunol. 2021 May 20;12:688301. doi: 10.3389/fimmu.2021.688301. eCollection 2021.
The presence of anti-human leucocyte antigen (HLA) antibodies in the potential solid organ transplant recipient's blood is one of the main barriers to access to a transplantation. The HLA sensitization is associated with longer waitlist time, antibody mediated rejection and transplant lost leading to increased recipient's morbidity and mortality. However, solid organ transplantation across the HLA immunological barriers have been reported in recipients who were highly sensitized to HLA using desensitization protocols. These desensitization regimens are focused on the reduction of circulating HLA antibodies. Despite those strategies improve rates of transplantation, it remains several limitations including persistent high rejection rate and worse long-term outcomes when compare with non-sensitized recipient population. Currently, interest is growing in the development of new desensitization approaches which, beyond targeting antibodies, would be based on the modulation of alloimmune pathways. Plasma cells appears as an interesting target given their critical role in antibody production. In the last decade, CD38-targeting immunotherapies, such as daratumumab, have been recognized as a key component in the treatment of myeloma by inducing an important plasma cell depletion. This review focuses on an emerging concept based on targeting CD38 to desensitize in the field of transplantation.
在潜在的实体器官移植受者的血液中存在抗人类白细胞抗原(HLA)抗体是获得移植的主要障碍之一。HLA 致敏与更长的等待名单时间、抗体介导的排斥反应和移植丢失有关,导致受者发病率和死亡率增加。然而,已经报道了在使用脱敏方案对 HLA 高度致敏的受者中进行跨越 HLA 免疫屏障的实体器官移植。这些脱敏方案侧重于减少循环 HLA 抗体。尽管这些策略提高了移植率,但仍存在一些局限性,包括与非致敏受者群体相比,持续的高排斥率和更差的长期结局。目前,人们对开发新的脱敏方法越来越感兴趣,这些方法除了针对抗体外,还将基于调节同种免疫途径。浆细胞因其在抗体产生中的关键作用而成为一个有趣的靶点。在过去十年中,CD38 靶向免疫疗法,如达雷妥尤单抗,已被认为是通过诱导重要的浆细胞耗竭来治疗骨髓瘤的关键组成部分。这篇综述侧重于基于 CD38 靶点在移植领域脱敏的新兴概念。