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Inactivation of dengue, chikungunya, and Ross River viruses in platelet concentrates after treatment with ultraviolet C light.

Identifieur interne : 003209 ( Ncbi/Merge ); précédent : 003208; suivant : 003210

Inactivation of dengue, chikungunya, and Ross River viruses in platelet concentrates after treatment with ultraviolet C light.

Auteurs : Helen M. Faddy ; Jesse J. Fryk ; Natalie A. Prow ; Daniel Watterson ; Paul R. Young ; Roy A. Hall ; Frank Tolksdorf [Allemagne] ; Chryslain Sumian [France] ; Ute Gravemann [Allemagne] ; Axel Seltsam [Allemagne] ; Denese C. Marks

Source :

RBID : pubmed:26926832

Descripteurs français

English descriptors

Abstract

Arboviruses, including dengue (DENV 1-4), chikungunya (CHIKV), and Ross River (RRV), are emerging viruses that are a risk for transfusion safety globally. An approach for managing this risk is pathogen inactivation, such as the THERAFLEX UV-Platelets system. We investigated the ability of this system to inactivate the above mentioned arboviruses.

DOI: 10.1111/trf.13519
PubMed: 26926832

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pubmed:26926832

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<term>Dengue Virus (radiation effects)</term>
<term>Dose-Response Relationship, Radiation</term>
<term>Humans</term>
<term>Limit of Detection</term>
<term>Platelet Transfusion (adverse effects)</term>
<term>Platelet Transfusion (standards)</term>
<term>RNA Viruses (radiation effects)</term>
<term>Ross River virus (radiation effects)</term>
<term>Ultraviolet Rays</term>
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<term>Humains</term>
<term>Inactivation virale (effets des radiations)</term>
<term>Limite de détection</term>
<term>Plaquettes (virologie)</term>
<term>Rayons ultraviolets</term>
<term>Relation dose-effet des radiations</term>
<term>Sécurité transfusionnelle ()</term>
<term>Transfusion de plaquettes (effets indésirables)</term>
<term>Transfusion de plaquettes (normes)</term>
<term>Virus de la dengue (effets des radiations)</term>
<term>Virus de la rivière Ross (effets des radiations)</term>
<term>Virus du chikungunya (effets des radiations)</term>
<term>Virus à ARN (effets des radiations)</term>
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<term>Platelet Transfusion</term>
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<term>Inactivation virale</term>
<term>Virus de la dengue</term>
<term>Virus de la rivière Ross</term>
<term>Virus du chikungunya</term>
<term>Virus à ARN</term>
</keywords>
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<term>Transfusion de plaquettes</term>
</keywords>
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<term>Blood Safety</term>
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<term>Transfusion de plaquettes</term>
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<term>Dengue Virus</term>
<term>RNA Viruses</term>
<term>Ross River virus</term>
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<term>Plaquettes</term>
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<term>Limit of Detection</term>
<term>Ultraviolet Rays</term>
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<term>Humains</term>
<term>Limite de détection</term>
<term>Rayons ultraviolets</term>
<term>Relation dose-effet des radiations</term>
<term>Sécurité transfusionnelle</term>
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<div type="abstract" xml:lang="en">Arboviruses, including dengue (DENV 1-4), chikungunya (CHIKV), and Ross River (RRV), are emerging viruses that are a risk for transfusion safety globally. An approach for managing this risk is pathogen inactivation, such as the THERAFLEX UV-Platelets system. We investigated the ability of this system to inactivate the above mentioned arboviruses.</div>
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<Year>2016</Year>
<Month>06</Month>
<Day>14</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>06</Month>
<Day>22</Day>
</DateCompleted>
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<Year>2017</Year>
<Month>06</Month>
<Day>22</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1537-2995</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>56</Volume>
<Issue>6 Pt 2</Issue>
<PubDate>
<Year>2016</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Transfusion</Title>
<ISOAbbreviation>Transfusion</ISOAbbreviation>
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<ArticleTitle>Inactivation of dengue, chikungunya, and Ross River viruses in platelet concentrates after treatment with ultraviolet C light.</ArticleTitle>
<Pagination>
<MedlinePgn>1548-55</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/trf.13519</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Arboviruses, including dengue (DENV 1-4), chikungunya (CHIKV), and Ross River (RRV), are emerging viruses that are a risk for transfusion safety globally. An approach for managing this risk is pathogen inactivation, such as the THERAFLEX UV-Platelets system. We investigated the ability of this system to inactivate the above mentioned arboviruses.</AbstractText>
<AbstractText Label="STUDY DESIGN AND METHODS" NlmCategory="METHODS">DENV 1-4, CHIKV, or RRV were spiked into buffy coat (BC)-derived platelet (PLT) concentrates in additive solution and treated with the THERAFLEX UV-Platelets system at the following doses: 0.05, 0.1, 0.15, and 0.2 J/cm(2) (standard dose). Pre- and posttreatment samples were taken for each dose, and the level of viral infectivity was determined.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">At the standard ultraviolet C (UVC) dose (0.2 J/cm(2) ), viral inactivation of at least 4.43, 6.34, and 5.13 log or more, was observed for DENV 1-4, CHIKV, and RRV, respectively. A dose dependency in viral inactivation was observed with increasing UVC doses.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Our study has shown that DENV, CHIKV, and RRV, spiked into BC-derived PLT concentrates, were inactivated by the THERAFLEX UV-Platelets system to the limit of detection of our assay, suggesting that this system could contribute to the safety of PLT concentrates with respect to these emerging arboviruses.</AbstractText>
<CopyrightInformation>© 2016 AABB.</CopyrightInformation>
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<LastName>Faddy</LastName>
<ForeName>Helen M</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>School of Medicine, University of Queensland, Brisbane, Queensland, Australia.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.</Affiliation>
</AffiliationInfo>
</Author>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
</Author>
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</AffiliationInfo>
</Author>
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<ForeName>Chryslain</ForeName>
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<AffiliationInfo>
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</AffiliationInfo>
</Author>
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<LastName>Gravemann</LastName>
<ForeName>Ute</ForeName>
<Initials>U</Initials>
<AffiliationInfo>
<Affiliation>German Red Cross Blood Service NSTOB, Springe, Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Seltsam</LastName>
<ForeName>Axel</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>German Red Cross Blood Service NSTOB, Springe, Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Marks</LastName>
<ForeName>Denese C</ForeName>
<Initials>DC</Initials>
<AffiliationInfo>
<Affiliation>Research and Development, Australian Red Cross Blood Service.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<PublicationType UI="D016428">Journal Article</PublicationType>
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<Year>2016</Year>
<Month>03</Month>
<Day>01</Day>
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<Country>United States</Country>
<MedlineTA>Transfusion</MedlineTA>
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<ISSNLinking>0041-1132</ISSNLinking>
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<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D001792" MajorTopicYN="N">Blood Platelets</DescriptorName>
<QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D058731" MajorTopicYN="N">Blood Safety</DescriptorName>
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<MeshHeading>
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</MeshHeading>
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<MeshHeading>
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