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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%">Rouet, F.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ménan, H.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Viljoen, J.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Ngo-Giang-Huong, Nicole</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Mandaliya, K.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Valéa, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lien, T. X.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Danaviah, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Rousset, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ganon, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Nerrienet, E.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>In-house HIV-1 RNA real-time RT-PCR assays : principle, available tests and usefulness in developing countries</title>
        <secondary-title>Expert Review of Molecular Diagnostics</secondary-title>
      </titles>
      <pages>635-650</pages>
      <keywords>
        <keyword>Developing country</keyword>
        <keyword>Genetic diversity</keyword>
        <keyword>Hiv-1</keyword>
        <keyword>Pcr</keyword>
        <keyword>Quantitative</keyword>
        <keyword>Real-time</keyword>
        <keyword>Reverse transcription</keyword>
        <keyword>Rna</keyword>
        <keyword>Viral load</keyword>
      </keywords>
      <dates>
        <year>2008</year>
      </dates>
      <call-num>fdi:010083650</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Expert Review of Molecular Diagnostics</full-title>
      </periodical>
      <isbn>1473-7159</isbn>
      <accession-num>ISI:000259749900010</accession-num>
      <number>5</number>
      <electronic-resource-num>10.1586/14737159.8.5.635</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010083650</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2021-11/010083650.pdf</url>
        </pdf-urls>
      </urls>
      <volume>8</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>The principle of currently available licensed HIV-1 RNA assays is based on real-time technologies that continuously monitor the fluorescence emitted by the amplification products. Besides these assays, in-house quantitative (q) real-time reverse transcription (RT)-PCR (RT-qPCR) tests have been developed and evaluated particularly in developing countries, for two main reasons. First, affordable and generalized access to HIV-1 RNA viral load is urgently needed in the context of expected universal access to prevention and antiretroviral treatment programs in these settings. Second, since many non-B subtypes, circulating recombinant forms and unique recombinant forms circulate in these areas, in-house HIV-1 RNA RT-qPCR assays are ideal academic tools to thoroughly evaluate the impact of HIV-1 genetic diversity on the accuracy of HIV-1 RNA quantification, as compared with licensed techniques. To date, at least 15 distinct in-house assays have been designed. They differ by their chemistry and the HIV-1 target sequence (located in gag, Pol-IN or LTR gene). Analytical performances of the tests that have been extensively evaluated appear at least as good as (or even better than) those of approved assays, with regard to HIV-1 strain diversity. Their clinical usefulness has been clearly demonstrated for early diagnosis of pediatric HIV-1 infection and monitoring of highly active antiretroviral therapy efficacy. The LTR-based HIV-1 RNA RT-qPCR assay has been evaluated by several groups under the auspices of the Agence Nationale de Recherches sur le SIDA et les hepatites virales B et C. It exists now as a complete standardized commercial test.</abstract>
      <custom6>052</custom6>
      <custom1>UR174</custom1>
      <custom7>Burkina Faso / Côte d'ivoire / Cameroun / Kenya / Cambodge / Vietnam / Afrique du Sud</custom7>
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