Bartel Ronnda L, Cramer Caryn, Ledford Kelly, Longcore Amy, Parrish Christopher, Stern Theresa, Watling Sharon, Zeigler Frank
Stem Cell Res Ther. 2012 Jul 9;3(4):26. doi: 10.1186/scrt117.
Aastrom Biosciences has developed a proprietary cell-processing technology that enables the manufacture of ixmyelocel-T, a patient-specific multicellular therapy expanded from a small sample of a patient's own bone marrow. Ixmyelocel-T is produced under current good manufacturing practices (cGMP) in a fully closed, automated system that expands mesenchymal stem cells (MSCs) and macrophages. While the cell types in ixmyelocel-T are the same as those found in the bone marrow, the numbers of MSCs and alternative macrophages are greater in ixmyelocel-T. We propose that the mixture of expanded MSCs and alternatively activated macrophages promote long-term tissue repair of ischemic tissue. The multiple cell types in ixmyelocel-T have a range of biological activities that are likely to contribute to a complex mechanism of action. Clinical trial data collected to date support the potential for ixmyelocel-T as an efficacious and safe treatment for ischemic cardiovascular indications, including critical limb ischemia (CLI) and a severe form of heart failure, dilated cardiomyopathy (DCM). The CLI clinical program has completed phase 2 and has reached concurrence with the Food and Drug Administration (FDA) on a phase 3 study (REVIVE) through the Special Protocol Assessment (SPA) process. The phase 3 study began screening patients in February 2012. The DCM clinical program will initiate phase 2b in 2012.
Aastrom生物科学公司已开发出一种专有的细胞处理技术,可用于制造ixmyelocel-T,这是一种针对患者的多细胞疗法,由患者自身骨髓的一小份样本扩增而来。Ixmyelocel-T是在当前良好生产规范(cGMP)下,在一个完全封闭的自动化系统中生产的,该系统可扩增间充质干细胞(MSC)和巨噬细胞。虽然ixmyelocel-T中的细胞类型与骨髓中的相同,但ixmyelocel-T中的MSC和替代性巨噬细胞数量更多。我们认为,扩增的MSC和替代性激活的巨噬细胞的混合物可促进缺血组织的长期组织修复。Ixmyelocel-T中的多种细胞类型具有一系列生物活性,可能有助于形成复杂的作用机制。迄今为止收集的临床试验数据支持ixmyelocel-T作为治疗缺血性心血管疾病(包括严重肢体缺血(CLI)和严重心力衰竭、扩张型心肌病(DCM))的有效且安全的治疗方法的潜力。CLI临床项目已完成2期研究,并通过特殊方案评估(SPA)程序与美国食品药品监督管理局(FDA)就3期研究(REVIVE)达成一致。3期研究于2012年2月开始筛选患者。DCM临床项目将于2012年启动2b期研究。