Acute toxicity study of Mesenchymal Stromal cells derived from Wharton’s Jelly in mouse by intravenous and subcutaneous route

Jaianand Kannaiyan, S. Narayanan, A. Pandey
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引用次数: 4

Abstract

: Aim: The present study was to evaluate the acute toxicity of WJ-MSCs in mouse by intravenous and subcutaneous route and to assess their potential for side effects, MLD, MTD and LD 50 . Objectives: Wide ranges of clinical and preclinical trials have suggested exploitation of adult MSCs for the cell-based reparative therapeutic approach; considering pros and cons of embryonic stem cells. However, for the clinical use existing adult stem cells source such as bone marrow, adipose tissue may be detrimental due to invasiveness in the procedure, less number of initial isolation and unsuitability for allogenic transplants. Recently fetal tissues such as Placenta, WJ have attracted as a good stem cell source due to its easy accessibility, ethical safety, immunological tolerance and large number of initial isolation of homogenous population necessary for increasing current market demand. Methods: In present study, we tried to work on complete characterization and up-scaling profiling of cells isolated from WJ, along with assessment of possible toxic effects of these cells when administered in-vivo and optimizing the route of administration with other clinical evaluation been addressed. Results: We confirmed that cells isolated from WJ exhibit morphologically and phenotypically similar properties as MSCs. The animal study also reveled that no mortality, no abnormal clinical signs and no remarkable pathological changes. Conclusion: Our animal toxicity study along with attempted rapid expansion of these cells to meet large clinical demands would allow them to be a lucrative candidate for clinical therapy.
华氏胶间充质间质细胞静脉注射和皮下注射对小鼠急性毒性研究
目的:研究WJ-MSCs经静脉和皮下两种途径对小鼠的急性毒性,并评价其潜在的毒副作用、MLD、MTD和ld50。目的:广泛的临床和临床前试验表明,利用成人间充质干细胞进行基于细胞的修复治疗;考虑胚胎干细胞的利弊。然而,对于临床使用现有的成体干细胞来源,如骨髓,脂肪组织可能是有害的,因为过程中的侵入性,初始分离次数较少,不适合同种异体移植。近年来,胎盘、WJ等胎儿组织因其易于获取、伦理安全、免疫耐受和大量同源群体的初始分离而成为当前市场需求增加所需的良好干细胞来源。方法:在目前的研究中,我们试图对从WJ中分离的细胞进行完整的表征和扩大规模的分析,同时评估这些细胞在体内给药时可能的毒性作用,并优化给药途径,同时进行其他临床评估。结果:我们证实从WJ分离的细胞表现出与MSCs相似的形态学和表型特性。动物实验无死亡,无临床异常体征,无明显病理改变。结论:我们的动物毒性研究以及尝试快速扩增这些细胞以满足大量临床需求,将使它们成为临床治疗中有利可图的候选细胞。
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