Vox Sanguinis · 2020 · 157 citations · 21 references
MedicineInfectious DiseasesMicrobiologyMolecular VirologyTransfusion MedicineVirologyBlood Component TherapyPlasma TransfusionPlatelet TransfusionTransfusion-transmitted InfectionsViral InfectionsVirus RemovalNipah Virus InfectionPathogen InfectivityPlasma SafetyPlasma Transfusion SafetyPlatelet Transfusion SafetyResidual Infectivity TestingSevere Acute Respiratory SyndromeUltraviolet Light Treatment
Background Emerging viruses like severe acute respiratory syndrome coronavirus (SARS‐CoV), Crimean–Congo haemorrhagic fever virus (CCHFV) and Nipah virus (NiV) have been identified to pose a potential threat to transfusion safety. In this study, the ability of the THERAFLEX UV‐Platelets and THERAFLEX MB‐Plasma pathogen inactivation systems to inactivate these viruses in platelet concentrates and plasma, respectively, was investigated. Materials and methods Blood products were spiked with SARS‐CoV, CCHFV or NiV, and then treated with increasing doses of UVC light (THERAFLEX UV‐Platelets) or with methylene blue (MB) plus increasing doses of visible light (MB/light; THERAFLEX MB‐Plasma). Samples were taken before and after treatment with each illumination dose and tested for residual infectivity. Results Treatment with half to three‐fourths of the full UVC dose (0·2 J/cm 2 ) reduced the infectivity of SARS‐CoV (≥3·4 log), CCHFV (≥2·2 log) and NiV (≥4·3 log) to the limit of detection (LOD) in platelet concentrates, and treatment with MB and a fourth of the full light dose (120 J/cm 2 ) decreased that of SARS‐CoV (≥3·1 log), CCHFV (≥3·2 log) and NiV (≥2·7 log) to the LOD in plasma. Conclusion Our study demonstrates that both THERAFLEX UV‐Platelets (UVC) and THERAFLEX MB‐Plasma (MB/light) effectively reduce the infectivity of SARS‐CoV, CCHFV and NiV in platelet concentrates and plasma, respectively.
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Vikrant Mankar, Amit B. Dhengre, Netranjali Agashe et al. · International Journal of Health Sciences · 2022 · 171 citations · Full text