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Identification and validation of multiple cell surface markers of clinical-grade adipose-derived mesenchymal stromal cells as novel release criteria for good manufacturing practice-compliant production

机译:鉴定和验证临床级脂肪间充质基质细胞的多种细胞表面标志物,作为符合良好生产规范的新型释放标准

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Background Clinical translation of mesenchymal stromal cells (MSCs) necessitates basic characterization of the cell product since variability in biological source and processing of MSCs may impact therapeutic outcomes. Although expression of classical cell surface markers (e.g., CD90, CD73, CD105, and CD44) is used to define MSCs, identification of functionally relevant cell surface markers would provide more robust release criteria and options for quality control. In addition, cell surface expression may distinguish between MSCs from different sources, including bone marrow-derived MSCs and clinical-grade adipose-derived MSCs (AMSCs) grown in human platelet lysate (hPL). Methods In this work we utilized quantitative PCR, flow cytometry, and RNA-sequencing to characterize AMSCs grown in hPL and validated non-classical markers in 15 clinical-grade donors. Results We characterized the surface marker transcriptome of AMSCs, validated the expression of classical markers, and identified nine non-classical markers (i.e., CD36, CD163, CD271, CD200, CD273, CD274, CD146, CD248, and CD140B) that may potentially discriminate AMSCs from other cell types. More importantly, these markers exhibit variability in cell surface expression among different cell isolates from a diverse cohort of donors, including freshly prepared, previously frozen, or proliferative state AMSCs and may be informative when manufacturing cells. Conclusions Our study establishes that clinical-grade AMSCs expanded in hPL represent a homogeneous cell culture population according to classical markers,. Additionally, we validated new biomarkers for further AMSC characterization that may provide novel information guiding the development of new release criteria. Clinical trials Use of Autologous Bone Marrow Aspirate Concentrate in Painful Knee Osteoarthritis (BMAC): Clinicaltrials.gov NCT01931007 . Registered August 26, 2013. MSC for Occlusive Disease of the Kidney: Clinicaltrials.gov NCT01840540 . Registered April 23, 2013. Mesenchymal Stem Cell Therapy in Multiple System Atrophy: Clinicaltrials.gov NCT02315027 . Registered October 31, 2014. Efficacy and Safety of Adult Human Mesenchymal Stem Cells to Treat Steroid Refractory Acute Graft Versus Host Disease. Clinicaltrials.gov NCT00366145 . Registered August 17, 2006. A Dose-escalation Safety Trial for Intrathecal Autologous Mesenchymal Stem Cell Therapy in Amyotrophic Lateral Sclerosis. Clinicaltrials.gov NCT01609283 . Registered May 18, 2012.
机译:背景技术间充质基质细胞(MSC)的临床翻译需要对细胞产物进行基本表征,因为MSC的生物来源和加工过程可能会影响治疗效果。尽管经典细胞表面标志物(例如CD90,CD73,CD105和CD44)的表达用于定义MSC,但功能相关的细胞表面标志物的鉴定将为质量控制提供更可靠的释放标准和选择。另外,细胞表面表达可以区分不同来源的MSC,包括骨髓源性MSC和人血小板裂解液(hPL)中生长的临床级脂肪源性MSC(AMSC)。方法在这项工作中,我们利用定量PCR,流式细胞仪和RNA测序来表征在hPL中生长的AMSC,并在15个临床级供体中验证了非经典标记。结果我们表征了AMSCs的表面标志物转录组,验证了经典标志物的表达,并鉴定了可能潜在区分的九种非经典标志物(即CD36,CD163,CD271,CD200,CD273,CD274,CD146,CD248和CD140B)其他细胞类型的AMSC。更重要的是,这些标记物在来自不同供者群体的不同细胞分离株之间的细胞表面表达中表现出差异,这些供体包括新鲜制备的,先前冷冻的或增殖状态的AMSC,在制造细胞时可能会提供信息。结论我们的研究表明,根据经典标记,在hPL中扩增的临床级AMSC代表了同质细胞培养群体。此外,我们验证了新的生物标记物,以用于进一步的AMSC表征,这可能会提供指导开发新释放标准的新颖信息。临床试验使用自体骨髓抽吸浓缩液治疗疼痛性膝骨关节炎(BMAC):Clinicaltrials.gov NCT01931007。注册于2013年8月26日。肾脏闭塞性疾病MSC:Clinicaltrials.gov NCT01840540。 2013年4月23日注册。多系统萎缩中的间充质干细胞治疗:Clinicaltrials.gov NCT02315027。 2014年10月31日注册。成人间充质干细胞治疗类固醇难治性急性移植物抗宿主病的功效和安全性。 Clinicaltrials.gov NCT00366145。 2006年8月17日注册。用于肌萎缩性侧索硬化的鞘内自体间充质干细胞疗法的剂量递增安全性试验。 Clinicaltrials.gov NCT01609283。 2012年5月18日注册。

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