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用于治疗移植物抗宿主病的Remestemcel-L

Remestemcel-L for the treatment of graft versus host disease.

作者信息

Locatelli F, Algeri M, Trevisan V, Bertaina A

机构信息

a Department of Pediatric Hematology-Oncology , IRCCS, Bambino Gesù Children's Hospital , Rome , Italy.

b Department of Pediatrics , University of Pavia , Pavia , Italy.

出版信息

Expert Rev Clin Immunol. 2017 Jan;13(1):43-56. doi: 10.1080/1744666X.2016.1208086. Epub 2016 Jul 29.

Abstract

Remestemcel-L, a third-party, off-the-shelf preparation of bone-marrow derived mesenchymal stromal cells (MSCs), has been developed for experimental use in acute graft-versus-host disease (aGvHD) and other immune-mediated conditions. Several preclinical and clinical studies have indeed suggested the potential of human mesenchymal stromal cells (MSCs) as an effective treatment for steroid-refractory aGvHD. However, an unambiguous demonstration of efficacy is still lacking. Areas covered: This review critically examines the biologic rationale supporting MSCs use in aGvHD and analyzes the results of published clinical trials in this setting, with a particular focus on the potential benefits and drawbacks of Remestemcel-L. For this purpose, a systematic literature search was performed in PubMed using the following keywords: 'mesenchymal stromal cells', 'mesenchymal progenitor cells', 'multipotent stromal cells', 'mesenchymal cells', 'MSC', 'Remestemcel-L', 'Prochymal', and 'graft-versus-host disease' or 'GvHD'. Expert commentary: Remestemcel-L represents a promising alternative to second-line immunosuppressive agents for the treatment of steroid-refractory aGvHD. Despite the safety and the favorable risk/benefit profile of this cell product, which has been demonstrated in several phase I-II studies, large and prospective randomized trials are required to confirm its efficacy in aGvHD and to define the optimal schedule of administration in terms of infusion timing, cell dose and pharmacological synergism.

摘要

Remestemcel-L是一种第三方现成的骨髓来源间充质基质细胞(MSC)制剂,已被开发用于急性移植物抗宿主病(aGvHD)及其他免疫介导病症的实验用途。多项临床前和临床研究确实提示了人间充质基质细胞(MSC)作为类固醇难治性aGvHD有效治疗方法的潜力。然而,仍缺乏疗效的确切证明。涵盖领域:本综述批判性地审视了支持在aGvHD中使用MSC的生物学原理,并分析了此背景下已发表临床试验的结果,特别关注Remestemcel-L的潜在益处和缺点。为此,在PubMed中使用以下关键词进行了系统的文献检索:“间充质基质细胞”、“间充质祖细胞”、“多能基质细胞”、“间充质细胞”、“MSC”、“Remestemcel-L”、“Prochymal”以及“移植物抗宿主病”或“GvHD”。专家评论:Remestemcel-L是治疗类固醇难治性aGvHD二线免疫抑制剂的一种有前景的替代物。尽管该细胞产品的安全性及良好的风险/效益特征已在多项I-II期研究中得到证实,但仍需要大型前瞻性随机试验来确认其在aGvHD中的疗效,并在输注时间、细胞剂量和药理协同作用方面确定最佳给药方案。

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