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        <identifier>oai:soar-ir.repo.nii.ac.jp:00003826</identifier>
        <datestamp>2022-12-14T04:39:56Z</datestamp>
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        <jpcoar:jpcoar xmlns:datacite="https://schema.datacite.org/meta/kernel-4/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcndl="http://ndl.go.jp/dcndl/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:jpcoar="https://github.com/JPCOAR/schema/blob/master/1.0/" xmlns:oaire="http://namespace.openaire.eu/schema/oaire/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:rioxxterms="http://www.rioxx.net/schema/v2.0/rioxxterms/" xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns="https://github.com/JPCOAR/schema/blob/master/1.0/" xsi:schemaLocation="https://github.com/JPCOAR/schema/blob/master/1.0/jpcoar_scm.xsd">
          <dc:title xml:lang="en">Serum chemokine levels are associated with the outcome of pegylated interferon and ribavirin therapy in patients with chronic hepatitis C</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Yoneda,  Suguru</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Umemura,  Takeji</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Joshita,  Satoru</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Ichijo,  Tetsuya</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Matsumoto,  Akihiro</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Yoshizawa,  Kaname</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Katsuyama,  Yoshihiko</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Ota,  Masao</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Tanaka,  Eiji</jpcoar:creatorName>
          </jpcoar:creator>
          <dc:rights>The definitive version is available at www.blackwell-synergy.com</dc:rights>
          <jpcoar:subject subjectScheme="Other">chemokines</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">core</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">interferon sensitivity determining region</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">MIP-1 beta</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">pegylated interferon</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">ribavirin</jpcoar:subject>
          <datacite:description descriptionType="Abstract">Aim: Serum chemokine levels and amino acid substitutions in the interferon-sensitivity determining region (ISDR) and core region have been associated with treatment outcome of pegylated interferon and ribavirin therapy in genotype 1 hepatitis C virus (HCV)-infected patients. The present study was conducted to clarify the association between serum chemokines and treatment outcome in patients with chronic HCV-1 infection in a Japanese cohort. Methods: A total of six serum chemokines were quantified before, during and after pegylated interferon and ribavirin treatment in 79 genotype 1 chronic HCV patients using a multiple bead array system. Viral ISDR and core region variants were determined by direct sequencing. Results: The baseline serum levels of eotaxin, IP-10 and RANTES were significantly higher in chronic HCV patients than in controls. High levels of eotaxin and macrophage inflammatory protein (MIP)-1 beta before therapy and more than two mutations in the ISDR were associated with a sustained virological response, and patients with more than two mutations in the ISDR also had significantly higher MIP-1 beta levels. Receiver-operator curve analysis showed a 77% sensitivity and 73% specificity for predicting an SVR using MIP-1 beta values. Conclusion: Serum MIP-1 beta levels may predict the response to HCV treatment with pegylated interferon and ribavirin and are associated with amino acid substitutions in the ISDR.</datacite:description>
          <dc:publisher>WILEY-BLACKWELL</dc:publisher>
          <datacite:date dateType="Issued">2011-06</datacite:date>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_6501">journal article</dc:type>
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          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/10091/16244</jpcoar:identifier>
          <jpcoar:identifier identifierType="URI">https://soar-ir.repo.nii.ac.jp/records/3826</jpcoar:identifier>
          <jpcoar:relation>
            <jpcoar:relatedIdentifier identifierType="PMID">https://pubmed.ncbi.nlm.nih.gov/21504519</jpcoar:relatedIdentifier>
            <jpcoar:relatedTitle>21504519</jpcoar:relatedTitle>
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          <jpcoar:relation>
            <jpcoar:relatedIdentifier identifierType="DOI">https://doi.org/10.1111/j.1872-034X.2011.00802.x</jpcoar:relatedIdentifier>
            <jpcoar:relatedTitle>10.1111/j.1872-034X.2011.00802.x</jpcoar:relatedTitle>
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          <jpcoar:sourceIdentifier identifierType="PISSN">1386-6346</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="NCID">AA11140867</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>HEPATOLOGY RESEARCH</jpcoar:sourceTitle>
          <jpcoar:volume>41</jpcoar:volume>
          <jpcoar:issue>6</jpcoar:issue>
          <jpcoar:pageStart>587</jpcoar:pageStart>
          <jpcoar:pageEnd>593</jpcoar:pageEnd>
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            <jpcoar:URI label="Serum_Chemokine_Levels_Are_Associated_Outcome_ Pegylated_Interferon.pdf">https://soar-ir.repo.nii.ac.jp/record/3826/files/Serum_Chemokine_Levels_Are_Associated_Outcome_ Pegylated_Interferon.pdf</jpcoar:URI>
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            <datacite:date dateType="Available">2015-09-24</datacite:date>
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