<?xml version="1.0" encoding="UTF-8"?>
<modsCollection xmlns="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd">
  <mods>
    <titleInfo>
      <title>Current progress in the prevention of mother-to-child transmission of hepatitis B and resulting clinical and programmatic implications</title>
    </titleInfo>
    <name type="personnal">
      <namePart type="family">Jourdain</namePart>
      <namePart type="given">Gonzague</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Ngo-Giang-Huong</namePart>
      <namePart type="given">Nicole</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Khamduang</namePart>
      <namePart type="given">W.</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <typeOfResource>text</typeOfResource>
    <genre authority="local">journalArticle</genre>
    <language>
      <languageTerm type="code" authority="iso639-2b">eng</languageTerm>
    </language>
    <physicalDescription>
      <internetMediaType>text/pdf</internetMediaType>
      <digitalOrigin>reformatted digital</digitalOrigin>
      <reformattingQuality>access</reformattingQuality>
    </physicalDescription>
    <abstract>There is currently no cure for hepatitis B chronic infections. Because new hepatitis B infections result mainly from perinatal transmission, preventing mother-to-child transmission is essential to reach by 2030 the goal of hepatitis B elimination set by the World Health Organization. The universal administration of hepatitis B vaccine to all infants, regardless of maternal status, starting with the birth dose, is the cornerstone of the strategy for elimination. Additional interventions, such as hepatitis B immune globulin administered to newborns and antiviral prophylaxis administered to hepatitis B infected pregnant women, may contribute to reaching the goal earlier. Hepatitis B immune globulin may remain out for reach of many pregnant women in low-and middle-income countries due to cost and logistic issues, but antivirals are cheap and do not require a cold chain for distribution. However, it has been observed that some viruses harbor mutations associated with escape from vaccine-elicited antibodies following immunization or administration of hepatitis B immune globulin. Also, resistance associated mutations have been described for several drugs used for treatment of hepatitis B infected patients as well as for the prevention of mother-to-child transmission. Whether these mutations have the potential to compromise the prevention of mother-to-child transmission or future treatment of the mother is a question of importance. We propose a review of important recent studies assessing tenofovir disoproxil fumarate for the prevention of mother-to-child transmission, and provides detailed information on the mutations possibly relevant in this setting.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>hepatitis B</topic>
      <topic>mother-to-child transmission</topic>
      <topic>prevention</topic>
      <topic>antiviral</topic>
      <topic>resistance</topic>
    </subject>
    <subject authority="local">
      <geographic>MONDE</geographic>
      <geographic>THAILANDE</geographic>
      <geographic>CHINE</geographic>
    </subject>
    <classification authority="local">052</classification>
    <classification authority="local">050</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Infection and Drug Resistance</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>12</number>
        </detail>
        <extent unit="pages">
          <list> 977-987</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2019</dateIssued>
      </originInfo>
      <identifier type="issn">1178-6973</identifier>
    </relatedItem>
    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010075690</identifier>
    <identifier type="doi">10.2147/idr.s171695</identifier>
    <identifier type="issn">1178-6973</identifier>
    <location>
      <shelfLocator>[F B010075690]</shelfLocator>
      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/fdi:010075690</url>
      <url access="row object">https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers19-05/010075690.pdf</url>
    </location>
    <recordInfo>
      <recordContentSource>IRD - Base Horizon / Pleins textes</recordContentSource>
      <recordCreationDate encoding="w3cdtf">2019-06-04</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2019-06-04</recordChangeDate>
      <recordIdentifier>fdi:010075690</recordIdentifier>
      <languageOfCataloging>
        <languageTerm authority="iso639-2b">fre</languageTerm>
      </languageOfCataloging>
    </recordInfo>
  </mods>
</modsCollection>
