Suppr超能文献

一份符合药品生产质量管理规范的角膜基质干细胞培养方案

A Full Good Manufacturing Practice-Compliant Protocol for Corneal Stromal Stem Cell Cultivation.

作者信息

Santra Mithun, Hsu Yen-Michael S, Khadem Shaheen, Radencic Sydney, Funderburgh Martha L, Sawant Onkar B, Dhaliwal Deepinder K, Jhanji Vishal, Yam Gary H F

机构信息

Corneal Regeneration Laboratory, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.

Immunologic Monitoring and Cellular Products Laboratory, Hillman Cancer Centre, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Bio Protoc. 2024 Sep 20;14(18):e5074. doi: 10.21769/BioProtoc.5074.

Abstract

Corneal scarring, a significant cause of global blindness, results from various insults, including trauma, infections, and genetic disorders. The conventional treatment to replace scarred corneal tissues includes partial or full-thickness corneal transplantation using healthy donor corneas. However, only 1 in 70 individuals with treatable corneal scarring can undergo surgery, due to the limited supply of transplantable donor tissue. Our research focuses on cell-based strategies, specifically ex vivo-expanded corneal stromal stem cells (CSSCs), to address corneal scarring. Preclinical studies have demonstrated the efficacy of CSSC treatment in reducing corneal inflammation and fibrosis, inhibiting scar formation, and regenerating native stromal tissue. Mechanisms include CSSC differentiation into stromal keratocytes and the expression of regenerative cytokines. Here, we present a good manufacturing practice (GMP)-compliant protocol to isolate and expand human CSSCs. This method paves the way to produce clinical-grade CSSCs for transplantation and clinical trials. Key features • This protocol utilizes surgical skills to dissect human corneal tissues for CSSC isolation. • The yield and features of CSSCs rely on donor tissue quality (freshness) and have donor-to-donor variability. • Up to 0.5 billion CSSCs can be generated from a single cornea specimen, and cells at passage 3 are suitable for treatment uses.

摘要

角膜瘢痕是全球失明的一个重要原因,它由各种损伤引起,包括创伤、感染和遗传疾病。替换瘢痕化角膜组织的传统治疗方法包括使用健康供体角膜进行部分或全层角膜移植。然而,由于可移植供体组织供应有限,每70名可治疗角膜瘢痕的患者中只有1人能够接受手术。我们的研究专注于基于细胞的策略,特别是体外扩增的角膜基质干细胞(CSSCs),以解决角膜瘢痕问题。临床前研究已经证明了CSSC治疗在减轻角膜炎症和纤维化、抑制瘢痕形成以及再生天然基质组织方面的疗效。其机制包括CSSC分化为基质角膜细胞以及再生细胞因子的表达。在此,我们提出一种符合药品生产质量管理规范(GMP)的方案来分离和扩增人CSSCs。该方法为生产用于移植和临床试验的临床级CSSCs铺平了道路。关键特性 • 本方案利用手术技巧解剖人角膜组织以分离CSSCs。 • CSSCs的产量和特性取决于供体组织质量(新鲜度),并且存在供体间差异。 • 从单个角膜标本中可产生多达5亿个CSSCs,第3代细胞适合用于治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3b4/11427334/b1238b096422/BioProtoc-14-18-5074-g001.jpg

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