确定含有间充质干细胞的生物医学细胞制剂真实性的算法

Q4 Biochemistry, Genetics and Molecular Biology
S. Druzhinina, M. Loginova, D. N. Smirnova, I. P. Obukhov, K. O. Yaroshenko, E. Poponina, E. Nazarova, N. Isaeva, I. Paramonov
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引用次数: 0

摘要

间充质干细胞(MSCs)具有显著的免疫调节活性,是生物医学细胞制剂的发展方向。在肿瘤血液学中,使用含有MSCs的BMCPs旨在支持与造血干细胞(hsc)共移植期间的造血功能,并抑制异体非相关移植和严重自身免疫过程中的免疫冲突。BMCPs注册的强制性阶段是确认MSC细胞系(CL)的身份,包括建立形态学特征,评估特定标记物和蛋白质的表达,以及确认培养过程中CL的遗传稳定性。遗传稳定性标记的测定方法多种多样,但根据美国国家标准化协会的建议,标准是短串联重复序列分析(STR分析)。本研究的目的是开发一种算法来确定含有MSCs的BMCPs的真实性,包括STR分析。材料和方法。根据国际细胞治疗协会的标准进行BMCP中MSC细胞的鉴定。活细胞在戈里亚耶夫室中计数。流式细胞术检测骨髓间充质干细胞的免疫表型。用酶免疫分析法评估特定蛋白的产生水平。通过STR分析鉴定遗传稳定性标记。结果和讨论。对10个BMCP样品进行了三次测试,以确认结果的重复性和可靠性。所开发的确定BMCP真实性的算法具有很高的准确性,因为它包括STR分析技术,这使得鉴定位于不同等位基因上的19个多态性STR标记成为可能。使用该方法将允许BMCP制造商通过国家药品注册程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Algorithm for determining the authenticity of biomedical cell preparations containing mesenchymal stem cells
The use of mesenchymal stem cells (MSCs), which have a pronounced immunomodulatory activity, is a promising direction in the development of biomedical cell preparations (BMCPs). In oncohematology, the use of BMCPs containing MSCs is aimed at supporting hematopoiesis during cotransplantation with hematopoietic stem cells (HSCs) and suppressing immune conflicts during allogeneic unrelated transplantation and severe autoimmune processes. An obligatory stage of registration of BMCPs is confirmation of the identity of the MSC cell line (CL), which includes the establishment of morphological characteristics, evaluation of the expression of specific markers and proteins, and confirmation of the genetic stability of CL during cultivation. Determination of markers of genetic stability is possible using various methods, however, according to the recommendations of the American National Standardization Institute, the standard is the analysis of short tandem repeats (STR analysis). The purpose of the study is to develop an algorithm for determining the authenticity of BMCPs containing MSCs, including STR analysis. Material and methods. Identification of MSC cells in BMCP was performed according to the criteria of the International Society for Cell Therapy. Viable cells were counted in a Goryaev chamber. Immunophenotypic characteristics of MSCs were determined by flow cytometry. The level of production of specific proteins was assessed using enzyme immunoassay. Genetic stability markers were identified by STR analysis. Results and discussion. The methods were tested in triplicate for ten BMCP samples to confirm the reproducibility and reliability of the results. The developed algorithm for determining the authenticity of BMCP has a high accuracy, as it includes the STR analysis technique, which makes it possible to identify 19 polymorphic STR markers located on different alleles. Using the method will allow BMCP manufacturers to go through the procedure of state registration of drugs.
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
54
审稿时长
12 weeks
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