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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Khamduang, W.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Gaudy-Graffin, C.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Ngo-Giang-Huong, Nicole</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Jourdain, Gonzague</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Moreau, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Luekamlung, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Halue, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Buranawanitchakorn, Y.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kunkongkapan, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Buranabanjasatean, S.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Lallemant, Marc</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sirirungsi, W.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Goudeau, A.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Long-term hepatitis B virus (HBV) response to lamivudine-containing highly active antiretroviral therapy in HIV-HBV co-infected patients in Thailand</title>
        <secondary-title>Plos One</secondary-title>
      </titles>
      <pages>e42184</pages>
      <keywords>
        <keyword>THAILANDE</keyword>
      </keywords>
      <dates>
        <year>2012</year>
      </dates>
      <call-num>fdi:010057143</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Plos One</full-title>
      </periodical>
      <isbn>1932-6203</isbn>
      <accession-num>ISI:000307045600071</accession-num>
      <number>7</number>
      <electronic-resource-num>10.1371/journal.pone.0042184</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010057143</url>
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        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers17-09/010057143.pdf</url>
        </pdf-urls>
      </urls>
      <volume>7</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background: Approximately 4 million of people are co-infected with HIV and Hepatitis B virus (HBV). In resource-limited settings, the majority of HIV-infected patients initiate first-line highly active antiretroviral therapy containing lamivudine (3TC-containing-HAART) and long-term virological response of HBV to lamivudine-containing HAART in co-infected patients is not well known. Methodology/Principal Finding: HIV-HBV co-infected patients enrolled in the PHPT cohort (ClinicalTrials. gov NCT00433030) and initiating a 3TC-containing-HAART regimen were included. HBV-DNA, HIV-RNA, CD4+ T-cell counts and alanine transaminase were measured at baseline, 3 months, 12 months and then every 6 months up to 5 years. Kaplan-Meier analysis was used to estimate the cumulative rates of patients who achieved and maintained HBV-DNA suppression. Of 30 co-infected patients, 19 were positive for HBe antigen (HBeAg). At initiation of 3TC-containing-HAART, median HBV DNA and HIV RNA levels were 7.35 log10 IU/mL and 4.47 log10 copies/mL, respectively. At 12 months, 67% of patients achieved HBV DNA suppression: 100% of HBeAg-negative patients and 47% of HBeAg-positive. Seventy-three percent of patients had HIV RNA below 50 copies/mL. The cumulative rates of maintained HBV-DNA suppression among the 23 patients who achieved HBV-DNA suppression were 91%, 87%, and 80% at 1, 2, and 4 years respectively. Of 17 patients who maintained HBV-DNA suppression while still on 3TC, 4 (24%) lost HBsAg and 7 of 8 (88%) HBeAg-positive patients lost HBeAg at their last visit (median duration, 59 months). HBV breakthrough was observed only in HBeAg-positive patients and 6 of 7 patients presenting HBV breakthrough had the rtM204I/V mutations associated with 3TC resistance along with rtL180M and/or rtV173L. Conclusions: All HBeAg-negative patients and 63% of HBeAg-positive HIV-HBV co-infected patients achieved long-term HBV DNA suppression while on 3TC-containing-HAART. This study provides information useful for the management of co-infected patients in resource-limited countries where the vast majority of co-infected patients are currently receiving 3TC.</abstract>
      <custom6>050 ; 052</custom6>
      <custom1>UR174</custom1>
      <custom7>Thaïlande</custom7>
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