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用于间充质基质细胞符合药品生产质量管理规范增殖的血小板衍生生长因子。

Platelet-derived growth factors for GMP-compliant propagation of mesenchymal stromal cells.

作者信息

Schallmoser Katharina, Rohde Eva, Bartmann Christina, Obenauf Anna C, Reinisch Andreas, Strunk Dirk

机构信息

Stem Cell Research Unit, Medical University of Graz, Austria.

出版信息

Biomed Mater Eng. 2009;19(4-5):271-6. doi: 10.3233/BME-2009-0591.

Abstract

Stem cell-based therapies are a promising prospect for regenerative medicine. Particularly, human multipotent mesenchymal stromal cells (MSCs) are currently in focus regarding their regenerative and immune modulating capacities. An increasing number of clinical trials investigating MSC efficiency and safety are ongoing. Ex vivo propagation of human MSCs is considered to be a prerequisite for MSC therapy. The to date standard use of fetal bovine serum in cell culture bears risks including xenoimmunization and transmission of pathogens. Alternatively, human platelet-derived growth factors have been efficiently implemented into routine MSC expansion protocols. In compliance with good manufacturing practice we established an effective time- and resource-saving procedure for MSC propagation in an animal serum-free system. Bone marrow was seeded without manipulation directly in pooled human platelet lysate (pHPL) and L-glutamine supplemented minimum essential medium without antibiotics. Clinical scale expanded MSCs were harvested already after primary culture. MSC quality, identity, purity and function were assessed according to a defined panel of release criteria and comparative genomic hybridization was used to determine genomic stability. Because various potential risks of MSCs have recently been reported, further research is required to prove efficiency and long-term safety of human MSCs for cell therapy.

摘要

基于干细胞的疗法是再生医学的一个有前景的方向。特别是,人类多能间充质基质细胞(MSCs)因其再生和免疫调节能力目前受到关注。越来越多研究MSCs有效性和安全性的临床试验正在进行。人类MSCs的体外扩增被认为是MSCs治疗的一个先决条件。迄今为止,细胞培养中使用胎牛血清存在包括异种免疫和病原体传播在内的风险。另外,人血小板衍生生长因子已被有效地应用于常规的MSCs扩增方案中。按照良好生产规范,我们建立了一种在无动物血清系统中有效节省时间和资源的MSCs扩增程序。将骨髓不经处理直接接种到添加了L-谷氨酰胺且无抗生素的人血小板裂解物(pHPL)和最低必需培养基的混合液中。临床规模扩增的MSCs在原代培养后即可收获。根据一组既定的放行标准评估MSCs的质量、特性、纯度和功能,并使用比较基因组杂交来确定基因组稳定性。由于最近报道了MSCs的各种潜在风险,需要进一步研究以证明人类MSCs用于细胞治疗的有效性和长期安全性。

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