Volume 59, Issue 4 pp. 1324-1332
BLOOD COMPONENTS

Bacterial inactivation of platelet concentrates with the THERAFLEX UV-Platelets pathogen inactivation system

Ute Gravemann

Ute Gravemann

German Red Cross Blood Service NSTOB, Institute Springe, Springe, Germany

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Wiebke Handke

Wiebke Handke

German Red Cross Blood Service NSTOB, Institute Springe, Springe, Germany

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Thomas H. Müller

Thomas H. Müller

German Red Cross Blood Service NSTOB, Institute Springe, Springe, Germany

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Axel Seltsam

Corresponding Author

Axel Seltsam

German Red Cross Blood Service NSTOB, Institute Springe, Springe, Germany

Address reprint requests to: Prof. Dr. Axel Seltsam, MD, MHBA, German Red Cross Blood Service NSTOB, Institute Springe, Eldagsener Strasse 38, 31832 Springe, Germany; e-mail: [email protected]Search for more papers by this author
First published: 26 December 2018
Citations: 22
This work was supported by the Research Foundation of the German Red Cross Blood Services (Deutsche Forschungsgemeinschaft der Blutspendedienste des Deutschen Roten Kreuzes) and Macopharma S.A.S.

Abstract

BACKGROUND

The THERAFLEX UV-Platelets system (Maco Pharma) uses ultraviolet C (UVC) light for pathogen inactivation (PI) of platelet concentrates (PCs) without any additional photoactive compound. The aim of the study was to systematically investigate bacterial inactivation with this system under conditions of intended use.

STUDY DESIGN AND METHODS

The robustness of the system was evaluated by assessing its capacity to inactivate high concentrations of different bacterial species in accordance with World Health Organization guidelines. The optimal use of the PI system was explored in time-to-treatment experiments by testing its ability to sterilize PCs contaminated with low levels of bacteria on the day of manufacture (target concentration, 100 colony-forming units/unit). The bacteria panel used for spiking experiments in this study included the World Health Organization International Repository Platelet Transfusion Relevant Reference Strains (n = 14), commercially available strains (n = 13), and in-house clinical isolates (n = 2).

RESULTS

Mean log reduction factors after UVC treatment ranged from 3.1 to 7.5 and varied between different strains of the same species. All PCs (n = 12/species) spiked with up to 200 colony-forming units/bag remained sterile until the end of storage when UVC treated 6 hours after spiking. UVC treatment 8 hours after spiking resulted in single breakthrough contaminations with the fast-growing species Escherichia coli and Streptococcus pyogenes.

CONCLUSION

The UVC-based THERAFLEX UV-Platelets system efficiently inactivates transfusion-relevant bacterial species in PCs. The comprehensive data from this study may provide a valuable basis for the optimal use of this UVC-based PI system.

CONFLICT OF INTEREST

UG, WH, THM, and AS received grants from the Research Foundation of the German Red Cross Blood Services (Deutsche Forschungsgemeinschaft der Blutspendedienste des Deutschen Roten Kreuzes) and Macopharma for the development of the UVC-based PI technology for platelets.

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