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使用商业间充质干细胞产品治疗激素难治性急性移植物抗宿主病。

Treatment of Steroid-Refractory Acute Graft--Host Disease Using Commercial Mesenchymal Stem Cell Products.

机构信息

Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo, Japan.

出版信息

Front Immunol. 2021 Aug 19;12:724380. doi: 10.3389/fimmu.2021.724380. eCollection 2021.

Abstract

Acute graft--host disease (GVHD) is a life-threatening complication that can develop after allogeneic hematopoietic stem cell transplantation. In particular, the prognosis of patients with steroid-refractory acute GVHD is extremely poor. Ryoncil™ (remestemcel-L), a human bone marrow-derived mesenchymal stem cell (MSC) product, failed to show superiority over placebo in patients with steroid-refractory acute GVHD, but it was approved for use in pediatric patients in Canada and New Zealand based on the results of a subgroup analysis. Temcell, an equivalent manufactured MSC product to remestemcel-L, was approved in Japan based on small single-arm studies by using a regulation for regenerative medicine in 2016. The efficacy of Temcell was evaluated in 381 consecutive patients treated with Temcell during the initial 3 years after its approval. Interestingly, its real-world efficacy was found to be equivalent to that observed in a prospective study of remestemcel-L with strict eligibility criteria. In this article, the potential of MSC therapy in the treatment of acute GVHD is discussed. A meticulous comparison of studies of remestemcel-L and Temcell, remestemcel-L/Temcell and ruxolitinib, and remestemcel-L/Temcell and thymoglobulin showed that the precise position of remestemcel-L/Temcell therapy in the treatment of acute GVHD remains to be determined.

摘要

急性移植物抗宿主病(GVHD)是一种危及生命的并发症,可发生于异基因造血干细胞移植后。特别是,类固醇难治性急性 GVHD 患者的预后极差。Ryoncil™(remestemcel-L)是人骨髓来源间充质干细胞(MSC)产品,在类固醇难治性急性 GVHD 患者中未显示优于安慰剂的疗效,但基于亚组分析结果,在加拿大和新西兰被批准用于儿科患者。Temcell 是与 remestemcel-L 等效的制造 MSC 产品,基于 2016 年再生医学监管规定,在日本被批准用于小单臂研究。在批准后的头 3 年中,对 381 例连续接受 Temcell 治疗的患者评估了 Temcell 的疗效。有趣的是,其真实世界的疗效与 remestemcel-L 的前瞻性研究中观察到的疗效相当,该研究有严格的入选标准。本文讨论了间充质干细胞疗法在急性 GVHD 治疗中的潜力。仔细比较了 remestemcel-L 和 Temcell、remestemcel-L/Temcell 和 ruxolitinib 以及 remestemcel-L/Temcell 和 thymoglobulin 的研究结果表明,remestemcel-L/Temcell 疗法在急性 GVHD 治疗中的精确位置仍有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d116/8417106/78ff7b7f3cc5/fimmu-12-724380-g001.jpg

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