Suppr超能文献

中国间充质干细胞/基质细胞新药临床试验申请用于移植物抗宿主病治疗的质量控制分析。

Quality Control Analysis of Mesenchymal Stem/Stromal Cells During Investigational New Drug Application for GvHD Administration in China.

机构信息

National Engineering Research Center of Cell Products, AmCellGene Engineering Co., Ltd., Tianjin, 300457, China.

Tianjin Key Laboratory of Engineering Technologies for Cell Pharmaceutical, Tianjin, 300457, China.

出版信息

Curr Stem Cell Res Ther. 2023;18(8):1032-1040. doi: 10.2174/1574888X17666220520155212.

Abstract

Graft-versus-host disease (GvHD), including the acute and chronic types (aGvHD, cGvHD), arise as the dominating secondary disease in patients with unsatisfying consequences of allogeneic hematopoietic stem cell transplantation (HSCT). Approximately half of GvHD patients were steroid-resistant, with a two-year overall survival rate lower than 20%. Worse still, there are no standardized criteria for an optimal second-line therapy for steroid-resistant aGVHD patients. Notably, pioneering investigators have highlighted the ameliorative or therapeutic effects of human umbilical cord-derived mesenchymal stem/stromal cells (hUC-MSCs) upon GvHD largely attributed to their unique hematopoietic-supporting and immunomodulatory properties. Of note, quality control (QC) is the prerequisite to assure the safety and quality of hUC-MSCs before investigational new drug (IND) applications and large-scale clinical applications. Herein, we summarize the state-of-the-art updates upon IND-associated QC and clinical trials of hUC-MSCs during allogeneic HSCT in China. Meanwhile, the supervisory policy and medical ethics of current licensed MSC products for GvHD administration and the concomitant opportunities and challenges have also been discussed.

摘要

移植物抗宿主病(GvHD),包括急性和慢性类型(aGvHD、cGvHD),是异基因造血干细胞移植(HSCT)后不满意的次要疾病,发生率较高。约一半的 GvHD 患者对类固醇耐药,两年总生存率低于 20%。更糟糕的是,对于类固醇耐药性 aGVHD 患者,没有标准化的二线治疗最佳标准。值得注意的是,开创性研究人员强调了人脐带来源间充质干细胞/基质细胞(hUC-MSCs)对 GvHD 的改善或治疗作用,主要归因于其独特的造血支持和免疫调节特性。值得注意的是,质量控制(QC)是在进行新药临床试验(IND)申请和大规模临床应用之前,确保 hUC-MSCs 安全性和质量的前提。在此,我们总结了在中国异基因 HSCT 期间与 IND 相关的 QC 和 hUC-MSCs 临床试验的最新进展。同时,还讨论了当前用于 GvHD 治疗的 MSC 产品的监管政策和医学伦理,以及伴随的机遇和挑战。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验