造血干细胞移植中使用间充质干细胞及其产品的最新情况

Al-Anazi Khalid Ahmed, Ayyad Ahmed, Kanfer Solaf
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引用次数: 0

摘要

移植物抗宿主疾病(GVHD)是异基因造血干细胞移植(HSCT)成功的主要限制因素,由于缺乏有效的二线疗法,类固醇难治性(SR)急性GVHD的预后很差。间充质干细胞(MSCs)具有免疫抑制、免疫调节和再生特性,在不久的将来可能成为治疗SR-GVHD的一种高效疗法。间充质干细胞在日本已被批准用于治疗儿童 SR-GVHD,在新西兰和加拿大也已获得有条件许可。预计欧洲、北美和世界其他地区将在几年内批准使用间充质干细胞治疗成人SR-GVHD。利用最近引进的技术,包括使用间充质干细胞产品(如外泌体和细胞外囊泡(ECVs))代替母体间充质干细胞、机器人制造技术和间充质干细胞基因工程,将最终克服间充质干细胞及其产品作为治疗手段广泛应用于造血干细胞移植和其他医疗领域所面临的障碍。本综述旨在介绍造血干细胞及其制品在造血干细胞移植领域应用所取得的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Update on the Use of Mesenchymal Stem Cells and their Products in Hematopoietic Stem Cell Transplantation
Graft Versus Host Disease (GVHD) is a major limitation to the success of allogeneic Hematopoietic Stem Cell Transplantation (HSCT) as Steroid-Refractory (SR) acute GVHD carries poor prognosis due to the absence of an efficacious second-line therapy. Mesenchymal Stem Cells (MSCs) which have immunosuppressive, immunomodulatory, and regenerative properties may become a highly effective therapeutic modality for SR-GVHD in the near future. MSCs have already been approved to treat childhood SR-GVHD in Japan, and they have been conditionally licensed in New Zealand and Canada. It is expected that MSCs will be approved for the treatment of SR-GVHD in adults in Europe, North America, and other parts of the world within a few years. Utilization of the recently introduced techniques including the use of MSC products such as exosomes and Extracellular Vesicles (ECVs) instead of the parent MSCs, robotic manufacturing technology, and genetic engineering of MSCs will ultimately overcome the remaining obstacles facing the widespread utilization of MSCs and their products as therapeutics not only in HSCT but also in other medical fields. The aim of this review is to provide an update on the remarkable progress achieved in the use of MSCs and their products in the field of HSCT.
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