Hanley Patrick J, Mei Zhuyong, Durett April G, Cabreira-Hansen Maria da Graca, Klis Mariola, Li Wei, Zhao Yali, Yang Bing, Parsha Kaushik, Mir Osman, Vahidy Farhaan, Bloom Debra, Rice R Brent, Hematti Peiman, Savitz Sean I, Gee Adrian P
Center for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and The Center for Cancer and Immunology Research, Children's National Medical Center, Washington, DC, USA.
Center for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
Cytotherapy. 2014 Aug;16(8):1048-58. doi: 10.1016/j.jcyt.2014.01.417. Epub 2014 Apr 13.
The use of bone marrow-derived mesenchymal stromal cells (MSCs) as a cellular therapy for various diseases, such as graft-versus-host disease, diabetes, ischemic cardiomyopathy and Crohn's disease, has produced promising results in early-phase clinical trials. However, for widespread application and use in later phase studies, manufacture of these cells must be cost-effective, safe and reproducible. Current methods of manufacturing in flasks or cell factories are labor-intensive, involve a large number of open procedures and require prolonged culture times.
We evaluated the Quantum Cell Expansion System for the expansion of large numbers of MSCs from unprocessed bone marrow in a functionally closed system and compared the results with a flask-based method currently in clinical trials.
After only two passages, we were able to expand a mean of 6.6 × 10(8) MSCs from 25 mL of bone marrow reproducibly. The mean expansion time was 21 days, and cells obtained were able to differentiate into all three lineages: chondrocytes, osteoblasts and adipocytes. The Quantum was able to generate the target cell number of 2.0 × 10(8) cells in an average of 9 fewer days and in half the number of passages required during flask-based expansion. We estimated that the Quantum would involve 133 open procedures versus 54,400 in flasks when manufacturing for a clinical trial. Quantum-expanded MSCs infused into an ischemic stroke rat model were therapeutically active.
The Quantum is a novel method of generating high numbers of MSCs in less time and at lower passages when compared with flasks. In the Quantum, the risk of contamination is substantially reduced because of the substantial decrease in open procedures.
将骨髓间充质基质细胞(MSC)用作针对多种疾病(如移植物抗宿主病、糖尿病、缺血性心肌病和克罗恩病)的细胞疗法,已在早期临床试验中取得了有前景的结果。然而,为了在广泛应用以及后期研究中使用,这些细胞的制造必须具有成本效益、安全且可重复。目前在培养瓶或细胞工厂中进行制造的方法劳动强度大,涉及大量开放操作步骤,且需要较长的培养时间。
我们评估了量子细胞扩增系统,用于在功能封闭系统中从未经处理的骨髓中扩增大量MSC,并将结果与目前正在临床试验中的基于培养瓶的方法进行比较。
仅经过两次传代,我们就能从25毫升骨髓中可重复地扩增出平均6.6×10⁸个MSC。平均扩增时间为21天,所获得的细胞能够分化为所有三种谱系:软骨细胞、成骨细胞和脂肪细胞。量子系统能够平均少用9天时间且在基于培养瓶扩增所需传代次数的一半时间内产生2.0×10⁸个目标细胞数量。我们估计,在为临床试验进行制造时,量子系统涉及133个开放操作步骤,而培养瓶则涉及54400个。注入缺血性中风大鼠模型的经量子系统扩增的MSC具有治疗活性。
与培养瓶相比,量子系统是一种在更短时间和更低传代次数下产生大量MSC的新方法。在量子系统中,由于开放操作步骤大幅减少,污染风险显著降低。