Robb Kevin P, Galipeau Jacques, Shi Yufang, Schuster Michael, Martin Ivan, Viswanathan Sowmya
Osteoarthritis Research Program, Division of Orthopedic Surgery, Schroeder Arthritis Institute, University Health Network, Toronto, Ontario, Canada; Krembil Research Institute, University Health Network, Toronto, Ontario, Canada; Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
Department of Medicine, School of Medicine and Public Health, University of Wisconsin in Madison, Madison, Wisconsin, USA; University of Wisconsin Carbone Comprehensive Cancer, University of Wisconsin in Madison, Madison, Wisconsin, USA.
Cytotherapy. 2024 May;26(5):413-417. doi: 10.1016/j.jcyt.2023.09.001. Epub 2023 Oct 7.
Mesenchymal stromal cells (MSCs) are promising cell therapy candidates, but their debated efficacy in clinical trials still limits successful adoption. Here, we discuss proceedings from a roundtable session titled "Failure to Launch Mesenchymal Stromal Cells 10 Years Later: What's on the Horizon?" held at the International Society for Cell & Gene Therapy 2023 Annual Meeting. Panelists discussed recent progress toward developing patient-stratification approaches for MSC treatments, highlighting the role of baseline levels of inflammation in mediating MSC treatment efficacy. In addition, MSC critical quality attributes (CQAs) are beginning to be elucidated and applied to investigational MSC products, including immunomodulatory functional assays and other potency markers that will help to ensure product consistency and quality. Lastly, next-generation MSC products, such as culture-priming strategies, were discussed as a promising strategy to augment MSC basal fitness and therapeutic potency. Key variables that will need to be considered alongside investigations of patient stratification approaches, CQAs and next-generation MSC products include the specific disease target being evaluated, route of administration of the cells and cell manufacturing parameters; these factors will have to be matched with postulated mechanisms of action towards treatment efficacy. Taken together, patient stratification metrics paired with the selection of therapeutically potent MSCs (using rigorous CQAs and/or engineered MSC products) represent a path forward to improve clinical successes and regulatory endorsements.
间充质基质细胞(MSCs)是很有前景的细胞治疗候选者,但其在临床试验中存在争议的疗效仍然限制了其成功应用。在此,我们讨论在2023年国际细胞与基因治疗协会年会上举行的题为“十年后间充质基质细胞未能成功推出:未来展望如何?”的圆桌会议的相关议程。小组成员讨论了在为MSC治疗开发患者分层方法方面的最新进展,强调了炎症基线水平在介导MSC治疗疗效中的作用。此外,MSC关键质量属性(CQAs)已开始得到阐明并应用于研究性MSC产品,包括免疫调节功能测定和其他效力标志物,这将有助于确保产品的一致性和质量。最后,讨论了下一代MSC产品,如培养预处理策略,作为增强MSC基础适应性和治疗效力的一种有前景的策略。在对患者分层方法、CQAs和下一代MSC产品进行研究时,需要考虑的关键变量包括正在评估的特定疾病靶点、细胞给药途径和细胞制造参数;这些因素必须与假定的治疗疗效作用机制相匹配。综上所述,将患者分层指标与治疗效力强的MSCs(使用严格的CQAs和/或工程化MSC产品)的选择相结合,代表了提高临床成功率和获得监管认可的前进方向。