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Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light.

Identifieur interne : 002798 ( PubMed/Corpus ); précédent : 002797; suivant : 002799

Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light.

Auteurs : Lily Lin ; Carl V. Hanson ; Harvey J. Alter ; Valérie Jauvin ; Kristen A. Bernard ; Krishna K. Murthy ; Peyton Metzel ; Laurence Corash

Source :

RBID : pubmed:15819680

English descriptors

Abstract

Viral contamination of platelet (PLT) concentrates can result in transfusion-transmitted diseases. A photochemical treatment (PCT) process with amotosalen-HCl and long-wavelength ultraviolet light (UVA), which cross-links nucleic acids, was developed to inactivate viruses and other pathogens in PLT concentrates.

DOI: 10.1111/j.0041-1132.2005.04316.x
PubMed: 15819680

Links to Exploration step

pubmed:15819680

Le document en format XML

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<title xml:lang="en">Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light.</title>
<author>
<name sortKey="Lin, Lily" sort="Lin, Lily" uniqKey="Lin L" first="Lily" last="Lin">Lily Lin</name>
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<nlm:affiliation>Cerus Corporation, Concord, California, USA. lily_lin@cerus.com</nlm:affiliation>
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</author>
<author>
<name sortKey="Hanson, Carl V" sort="Hanson, Carl V" uniqKey="Hanson C" first="Carl V" last="Hanson">Carl V. Hanson</name>
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<name sortKey="Alter, Harvey J" sort="Alter, Harvey J" uniqKey="Alter H" first="Harvey J" last="Alter">Harvey J. Alter</name>
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<author>
<name sortKey="Jauvin, Valerie" sort="Jauvin, Valerie" uniqKey="Jauvin V" first="Valérie" last="Jauvin">Valérie Jauvin</name>
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<name sortKey="Bernard, Kristen A" sort="Bernard, Kristen A" uniqKey="Bernard K" first="Kristen A" last="Bernard">Kristen A. Bernard</name>
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<name sortKey="Murthy, Krishna K" sort="Murthy, Krishna K" uniqKey="Murthy K" first="Krishna K" last="Murthy">Krishna K. Murthy</name>
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<name sortKey="Metzel, Peyton" sort="Metzel, Peyton" uniqKey="Metzel P" first="Peyton" last="Metzel">Peyton Metzel</name>
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<name sortKey="Corash, Laurence" sort="Corash, Laurence" uniqKey="Corash L" first="Laurence" last="Corash">Laurence Corash</name>
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<title xml:lang="en">Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light.</title>
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<name sortKey="Bernard, Kristen A" sort="Bernard, Kristen A" uniqKey="Bernard K" first="Kristen A" last="Bernard">Kristen A. Bernard</name>
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<name sortKey="Corash, Laurence" sort="Corash, Laurence" uniqKey="Corash L" first="Laurence" last="Corash">Laurence Corash</name>
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<title level="j">Transfusion</title>
<idno type="ISSN">0041-1132</idno>
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<term>Blood Banks (methods)</term>
<term>Furocoumarins (pharmacology)</term>
<term>Humans</term>
<term>In Vitro Techniques</term>
<term>Platelet Transfusion</term>
<term>Ultraviolet Rays</term>
<term>Virus Diseases (blood)</term>
<term>Virus Diseases (prevention & control)</term>
<term>Virus Diseases (transmission)</term>
<term>Virus Replication (drug effects)</term>
<term>Virus Replication (radiation effects)</term>
<term>Viruses (drug effects)</term>
<term>Viruses (growth & development)</term>
<term>Viruses (radiation effects)</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Furocoumarins</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en">
<term>Virus Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Virus Replication</term>
<term>Viruses</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en">
<term>Viruses</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Blood Banks</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Virus Diseases</term>
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<term>Virus Replication</term>
<term>Viruses</term>
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<term>Virus Diseases</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Humans</term>
<term>In Vitro Techniques</term>
<term>Platelet Transfusion</term>
<term>Ultraviolet Rays</term>
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<div type="abstract" xml:lang="en">Viral contamination of platelet (PLT) concentrates can result in transfusion-transmitted diseases. A photochemical treatment (PCT) process with amotosalen-HCl and long-wavelength ultraviolet light (UVA), which cross-links nucleic acids, was developed to inactivate viruses and other pathogens in PLT concentrates.</div>
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<PMID Version="1">15819680</PMID>
<DateCompleted>
<Year>2005</Year>
<Month>05</Month>
<Day>10</Day>
</DateCompleted>
<DateRevised>
<Year>2014</Year>
<Month>11</Month>
<Day>20</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">0041-1132</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>45</Volume>
<Issue>4</Issue>
<PubDate>
<Year>2005</Year>
<Month>Apr</Month>
</PubDate>
</JournalIssue>
<Title>Transfusion</Title>
<ISOAbbreviation>Transfusion</ISOAbbreviation>
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<ArticleTitle>Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light.</ArticleTitle>
<Pagination>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Viral contamination of platelet (PLT) concentrates can result in transfusion-transmitted diseases. A photochemical treatment (PCT) process with amotosalen-HCl and long-wavelength ultraviolet light (UVA), which cross-links nucleic acids, was developed to inactivate viruses and other pathogens in PLT concentrates.</AbstractText>
<AbstractText Label="STUDY DESIGN AND METHODS" NlmCategory="METHODS">High titers of pathogenic or blood-borne viruses, representing 10 different families, were added to single-donor PLT concentrates containing 3.0 x 10(11) to 6.0 x 10(11) PLTs in approximately 300 mL of 35 percent plasma and 65 percent PLT additive solution (InterSol). After PCT with 150 micromol per L amotosalen and 3 J per cm(2) UVA, residual viral infectivity was assayed by sensitive cell culture or animal systems.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Enveloped viruses were uniformly sensitive to inactivation by PCT whereas nonenveloped viruses demonstrated variable inactivation. Log reduction of enveloped viruses for cell-free HIV-1 was >6.2; for cell-associated HIV-1, >6.1; for clinical isolate HIV-1, >3.4; for clinical isolate HIV-2, >2.5; for HBV, >5.5; for HCV, >4.5; for DHBV, >6.2; for BVDV, >6.0; for HTLV-I, 4.2; for HTLV-II, 4.6; for CMV, >5.9; for WNV, >5.5; for SARS-HCoV, >5.8; and for vaccinia virus, >4.7. Log reduction of nonenveloped viruses for human adenovirus 5 was >5.2; for parvovirus B19, 3.5->5.0; for bluetongue virus, 5.6-5.9; for feline conjunctivitis virus, 1.7-2.4; and for simian adenovirus 15, 0.7-2.3.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">PCT inactivates a broad spectrum of pathogenic, blood-borne viruses. Inactivation of viruses in PLT concentrates with amotosalen and UVA offers the potential to prospectively prevent the majority of PLT transfusion-associated viral diseases.</AbstractText>
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<DescriptorName UI="D017713" MajorTopicYN="Y">Platelet Transfusion</DescriptorName>
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