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脂肪来源干细胞基药物制剂的微生物学方面。

Microbiological Aspects of Pharmaceutical Manufacturing of Adipose-Derived Stem Cell-Based Medicinal Products.

机构信息

Laboratory for Cell Research and Application, Center for Preclinical Research and Technology, Medical University of Warsaw, Banacha 1b, 02-097 Warsaw, Poland.

BBMRI.pl Consortium, 61 Żwirki i Wigury Street, 02-091 Warsaw, Poland.

出版信息

Cells. 2023 Feb 21;12(5):680. doi: 10.3390/cells12050680.

Abstract

Subcutaneous adipose tissue is an excellent source of mesenchymal stem cells (ADSCs), which can be used in cell therapies as an active substance in advanced therapy medicinal products (ATMPs). Because of the short shelf-life of ATMPs and the time needed to obtain the results of microbiological analysis, the final product is often administered to the patient before sterility is confirmed. Because the tissue used for cell isolation is not sterilized to maintain cell viability, controlling and ensuring microbiological purity at all stages of production is crucial. This study presents the results of monitoring the contamination incidence during ADSC-based ATMP manufacturing over two years. It was found that more than 40% of lipoaspirates were contaminated with thirteen different microorganisms, which were identified as being physiological flora from human skin. Such contamination was successfully eliminated from the final ATMPs through the implementation of additional microbiological monitoring and decontamination steps at various stages of production. Environmental monitoring revealed incidental bacterial or fungal growth, which did not result in any product contamination and was reduced thanks to an effective quality assurance system. To conclude, the tissue used for ADSC-based ATMP manufacturing should be considered contaminated; therefore, good manufacturing practices specific to this type of product must be elaborated and implemented by the manufacturer and the clinic in order to obtain a sterile product.

摘要

皮下脂肪组织是间充质干细胞(ADSCs)的绝佳来源,可作为先进治疗药物产品(ATMP)中的活性物质用于细胞治疗。由于 ATMP 的保质期短,并且需要获得微生物分析结果的时间,因此最终产品通常在确认无菌性之前施用于患者。由于用于细胞分离的组织未进行灭菌以保持细胞活力,因此在生产的所有阶段控制和确保微生物纯度至关重要。本研究介绍了两年间监测基于 ADSC 的 ATMP 生产过程中污染发生率的结果。结果发现,超过 40%的脂肪抽吸物受到十三种不同微生物的污染,这些微生物被鉴定为来自人体皮肤的生理性菌群。通过在生产的各个阶段实施额外的微生物监测和去污步骤,成功地从最终的 ATMP 中消除了这种污染。环境监测显示偶然的细菌或真菌生长,但并未导致任何产品污染,并由于有效的质量保证体系而得到减少。总之,用于基于 ADSC 的 ATMP 制造的组织应被视为污染组织;因此,制造商和临床医生必须制定并实施特定于此类产品的良好生产规范,以获得无菌产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77e9/10000438/ac18b753f408/cells-12-00680-g001a.jpg

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