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    <titleInfo>
      <title>Response to conjugate #Haemophilus influenzae$ B vaccine among infants in Niamey, Niger</title>
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      <namePart type="given">Jean-Philippe</namePart>
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    <abstract>Despite near elimination of Haemophilus influenzae b (Hib) meningitis from several industrialized countries following introduction of conjugate Hib vaccines into infant immunization schedules, Hib remains a major cause of meningitis and pneumonia in resource-poor countries. In Niger, Hib causes nearly 200 cases of meningitis per 100,000 children &lt; one year of age, and &gt; 40% of cases are fatal. We evaluated the immunogenicity of Hib polysaccharide-tetanus toxoid conjugate vaccine (PRP-T) administered in the same syringe as diphtheria-tetanus-pertussis (DTP) vaccine among infants in Niger. Infants were randomized into group 1 (PRP-T at six, 10, and 14 weeks), group 2 (PRP-T at 10 and 14 weeks), or a control group (meningococcal A/C polysaccharide vaccine). By 14 weeks of age, all subjects in groups 1 and 2 had 0.15 or more microg/ml of anti-PRP antibody, and 82% versus 76% had 1.0 or more microg/ml of antibody (P = not significant). By nine months of age the proportion of infants with 0.15 or more and 1.0 or more microg/ml was group 1 = 97% and 76% ; group 2 = 93% and 67% ; controls = 10% and 2.6%. Four weeks after the first, second, and third doses of PRP-T, infants in group 1 showed geometric mean titers (GMTs) of 0.19, 3.97, and 6.09 microg/ml while infants in group 2 had GMTs of 2.40 and 4.41 microg/ml four weeks after the delayed first and second doses. Both PRP-T groups had significantly higher GMTs at 18 weeks and nine months of age than infants in the control group. The Hib PRP-T vaccine was immunogenic in infants in Niger. The strong response after PRP-T was initiated one month after the first DTP vaccination may reflect carrier priming. Two dose schedules of PRP-T should be given serious consideration, particularly if their reduced cost permits vaccine introduction that would be otherwise unaffordable. (Résumé d'auteur)</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject authority="local">
      <topic>SANTE PUBLIQUE</topic>
      <topic>VACCINATION</topic>
      <topic>NOURRISSON</topic>
      <topic>ANTICORPS</topic>
      <topic>DOSAGE</topic>
      <topic>EFFICACITE</topic>
      <topic>ANALYSE STATISTIQUE</topic>
    </subject>
    <subject>
      <topic>MENINGITE</topic>
    </subject>
    <subject authority="local">
      <geographic>NIGER</geographic>
      <geographic>NIAMEY</geographic>
    </subject>
    <classification authority="local">052MALTRA05</classification>
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      <part>
        <detail type="volume">
          <number>59</number>
        </detail>
        <detail type="volume">
          <number>5</number>
        </detail>
        <extent unit="pages">
          <list> 837-842</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>1998</dateIssued>
      </originInfo>
      <identifier type="issn">0002-9637</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010016144</identifier>
    <identifier type="issn">0002-9637</identifier>
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      <url access="row object">https://horizon.documentation.ird.fr/exl-doc/pleins_textes/pleins_textes_7/b_fdi_53-54/010016144.pdf</url>
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      <recordCreationDate encoding="w3cdtf">1998-12-07</recordCreationDate>
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      <recordIdentifier>fdi:010016144</recordIdentifier>
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        <languageTerm authority="iso639-2b">fre</languageTerm>
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