LYSAK, D., M. HOLUBOVA, T. BERGEROVA, M. VAVROVA, G. C. CANGEMI, R. CICCOCIOPPO, Peter KRUŽLIAK and P. JINDRA. Validation of shortened 2-day sterility testing of mesenchymal stem cell-based therapeutic preparation on an automated culture system. Cell and Tissue Banking. Dordrecht: Springer, 2016, vol. 17, No 1, p. 1-9. ISSN 1389-9333. Available from: https://dx.doi.org/10.1007/s10561-015-9522-9.
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Basic information
Original name Validation of shortened 2-day sterility testing of mesenchymal stem cell-based therapeutic preparation on an automated culture system
Authors LYSAK, D. (203 Czech Republic), M. HOLUBOVA (203 Czech Republic), T. BERGEROVA (203 Czech Republic), M. VAVROVA (203 Czech Republic), G. C. CANGEMI (380 Italy), R. CICCOCIOPPO (380 Italy), Peter KRUŽLIAK (703 Slovakia, guarantor, belonging to the institution) and P. JINDRA (203 Czech Republic).
Edition Cell and Tissue Banking, Dordrecht, Springer, 2016, 1389-9333.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10601 Cell biology
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 1.331
RIV identification code RIV/00216224:14110/16:00113811
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1007/s10561-015-9522-9
UT WoS 000372277400001
Keywords in English Automated culture system; Cell therapy; Mesenchymal stem cells; Sterility; Validation
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 27/4/2020 15:36.
Abstract
Cell therapy products represent a new trend of treatment in the field of immunotherapy and regenerative medicine. Their biological nature and multistep preparation procedure require the application of complex release criteria and quality control. Microbial contamination of cell therapy products is a potential source of morbidity in recipients. The automated blood culture systems are widely used for the detection of microorganisms in cell therapy products. However the standard 2-week cultivation period is too long for some cell-based treatments and alternative methods have to be devised. We tried to verify whether a shortened cultivation of the supernatant from the mesenchymal stem cell (MSC) culture obtained 2 days before the cell harvest could sufficiently detect microbial growth and allow the release of MSC for clinical application. We compared the standard Ph. Eur. cultivation method and the automated blood culture system BACTEC (Becton Dickinson). The time to detection (TTD) and the detection limit were analyzed for three bacterial and two fungal strains. The Staphylococcus aureus and Pseudomonas aeruginosa were recognized within 24 h with both methods (detection limit similar to 10 CFU). The time required for the detection of Bacillus subtilis was shorter with the automated method (TTD 10.3 vs. 60 h for 10-100 CFU). The BACTEC system reached significantly shorter times to the detection of Candida albicans and Aspergillus brasiliensis growth compared to the classical method (15.5 vs. 48 and 31.5 vs. 48 h, respectively; 10-100 CFU). The positivity was demonstrated within 48 h in all bottles, regardless of the size of the inoculum. This study validated the automated cultivation system as a method able to detect all tested microorganisms within a 48-h period with a detection limit of similar to 10 CFU. Only in case of B. subtilis, the lowest inoculum (similar to 10 CFU) was not recognized. The 2-day cultivation technique is then capable of confirming the microbiological safety of MSC and allows their timely release for clinical application.
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