Journal article
Inactivation of SARS-CoV-2 infectivity in platelet concentrates or plasma following treatment with ultraviolet C light or with methylene blue combined with visible light
Transfusion, Vol.63(2), pp.288-293
2023
PMCID: PMC9880728
PMID: 36573801
Abstract
Background:
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is unlikely to be a major transfusion-transmitted pathogen; however, convalescent plasma is a treatment option used in some regions. The risk of transfusion-transmitted infections can be minimized by implementing Pathogen Inactivation (PI), such as THERAFLEX MB-plasma and THERAFLEX UV-Platelets systems. Here we examined the capability of these PI systems to inactivate SARS-CoV-2.
Study Design and Methods:
SARS-CoV-2 spiked plasma units were treated using the THERAFLEX MB-Plasma system in the presence of methylene blue (~0.8 μmol/L; visible light doses: 20, 40, 60, and 120 [standard] J/cm2). SARS-CoV-2 spiked platelet concentrates (PCs) were treated using the THERAFLEX UV-platelets system (UVC doses: 0.05, 0.10, 0.15, and 0.20 [standard] J/cm2). Samples were taken prior to the first and after each illumination dose, and viral infectivity was assessed using an immunoplaque assay.
Results:
Treatment of spiked plasma with the THERAFLEX MB-Plasma system resulted in an average ≥5.03 log10 reduction in SARS-CoV-2 infectivity at one third (40 J/cm2) of the standard visible light dose. For the platelet concentrates (PCs), treatment with the THERAFLEX UV-Platelets system resulted in an average ≥5.18 log10 reduction in SARS-CoV-2 infectivity at the standard UVC dose (0.2 J/cm2).
Conclusions:
SARS-CoV-2 infectivity was reduced in plasma and platelets following treatment with the THERAFLEX MB-Plasma and THERAFLEX UV-Platelets systems, to the limit of detection, respectively. These PI technologies could therefore be an effective option to reduce the risk of transfusion-transmitted emerging pathogens.
Details
- Title
- Inactivation of SARS-CoV-2 infectivity in platelet concentrates or plasma following treatment with ultraviolet C light or with methylene blue combined with visible light
- Authors
- Jody Hobson-Peters (Corresponding Author) - The University of QueenslandAlberto A Amarilla (Author) - The University of QueenslandLina Rustanti (Author) - Australian Red Cross LifebloodDenese C Marks (Author) - Australian Red Cross LifebloodEileen Roulis (Author) - Australian Red Cross LifebloodAlexander A Khromykh (Author) - The University of QueenslandNaphak Modhiran (Author) - School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, AustraliaDaniel Watterson (Author) - Australian Infectious Diseases Research Centre, Global Virus Network Centre of Excellence, Brisbane, QLD, AustraliaStefan Reichenberg (Author) - Macopharma International GmbH, Langen, GermanyFrank Tolksdorf (Author) - Macopharma International GmbH, Langen, GermanyChryslain Sumian (Author) - Macopharma (France)Axel Seltsam (Author) - Bavarian Red Cross Blood Service, Nuremberg, GermanyUte Gravemann (Author) - German Red Cross Blood Service NSTOB, Springe, GermanyHelen M Faddy (Author) - University of the Sunshine Coast, Queensland, School of Health - Biomedicine
- Publication details
- Transfusion, Vol.63(2), pp.288-293
- Publisher
- Wiley-Blackwell Publishing, Inc.
- Date published
- 2023
- DOI
- 10.1111/trf.17238
- ISSN
- 1537-2995
- PMID
- 36573801; PMC9880728
- Copyright note
- This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. © 2023 The Authors. Transfusion published by Wiley Periodicals LLC on behalf of AABB.
- Organisation Unit
- School of Health - Biomedicine; School of Health and Behavioural Sciences - Legacy
- Language
- English
- Record Identifier
- 99698697802621
- Output Type
- Journal article
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