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Inactivation of dengue virus in plasma with amotosalen and ultraviolet A illumination.

AbstractBACKGROUND:
Dengue virus (DENV) is the most prevalent arbovirus in tropical and subtropical regions. Transfusion-transmitted DENV infections have already been reported and the risk for blood products to be contaminated by DENV needs to be considered in dengue-endemic areas, especially during outbreaks. Blood product inactivation processes, including amotosalen and ultraviolet A (UVA) illumination, have been developed to reduce transfusion-transmitted infections. In this study we demonstrate the efficiency of using amotosalen and UVA illumination for DENV inactivation in human plasma.
STUDY DESIGN AND METHODS:
Plasma units from volunteer blood donors were spiked with DENV. Viral titers and viral RNA loads were measured in plasma before and after amotosalen and UVA photochemical treatment.
RESULTS:
The mean DENV titer in plasma before inactivation was 5.61 log 50% tissue culture infectious dose (TCID50)/mL and the mean viral RNA load was 10.21 log copies/mL. In inactivated plasma, the mean DENV RNA load was 9.37 log copies/mL, but cell cultures inoculated with inactivated plasma did not result in infected cells and did not produce any replicative virus nor detectable viral RNA.
CONCLUSION:
We report here that amotosalen combined with UVA light inactivated DENV in fresh-frozen plasma (5.61 log inactivation of viral titer). This inactivation process is an efficient method to prevent plasma transfusion-transmitted DENV infections.
AuthorsDidier Musso, Vaea Richard, Julien Broult, Van-Mai Cao-Lormeau
JournalTransfusion (Transfusion) Vol. 54 Issue 11 Pg. 2924-30 (Nov 2014) ISSN: 1537-2995 [Electronic] United States
PMID24845685 (Publication Type: Clinical Trial, Journal Article)
Copyright© 2014 AABB.
Chemical References
  • Furocoumarins
  • Photosensitizing Agents
  • RNA, Viral
  • amotosalen
Topics
  • Blood Component Transfusion
  • Blood Donors
  • Blood Safety
  • Dengue (prevention & control, transmission)
  • Dengue Virus
  • Female
  • Furocoumarins (pharmacology)
  • Humans
  • Male
  • Photosensitizing Agents (pharmacology)
  • Plasma (virology)
  • Polynesia
  • RNA, Viral (blood)
  • Ultraviolet Rays
  • Virus Inactivation (drug effects, radiation effects)

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