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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACLN : Articles dans des revues avec comité de lecture non répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Campagne, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Garba, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Fabre, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Schuchat, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ryall, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Boulanger, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bybel, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Carlone, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Briantais, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ivanoff, B.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Xerri, B.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Chippaux, Jean-Philippe</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Safety and immunogenicity of three doses of a Neisseria meningitidis A + C diphtheria conjugate vaccine in infants from Niger</title>
        <secondary-title>Pediatric Infectious Disease Journal</secondary-title>
      </titles>
      <pages>144-150</pages>
      <keywords>
        <keyword>EPIDEMIE</keyword>
        <keyword>ENFANT D'AGE PRESCOLAIRE</keyword>
        <keyword>VACCINATION</keyword>
        <keyword>DOSE</keyword>
        <keyword>TOXICITE</keyword>
        <keyword>IMMUNITE</keyword>
        <keyword>METHODE D'ANALYSE</keyword>
        <keyword>TEST ELISA</keyword>
        <keyword>TEST BIOLOGIQUE</keyword>
        <keyword>ETUDE EXPERIMENTALE</keyword>
        <keyword>ETUDE COMPARATIVE</keyword>
        <keyword>MENINGITE</keyword>
        <keyword>MEND</keyword>
        <keyword>MENPS</keyword>
        <keyword>PRP T</keyword>
        <keyword>NIGER</keyword>
        <keyword>NIAMEY</keyword>
      </keywords>
      <dates>
        <year>2000</year>
      </dates>
      <call-num>fdi:010026109</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Pediatric Infectious Disease Journal</full-title>
      </periodical>
      <isbn>0891-3668</isbn>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010026109</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/pleins_textes_7/b_fdi_59-60/010026109.pdf</url>
        </pdf-urls>
      </urls>
      <volume>19</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background : High rates of endemic disease and recurrent epidemics of serogroup A and C meningococcal meningitis continue to occur in sub-Saharan Africa. A meningococcal A+ + C polysaccharide diptheria-toxoid-conjugated vaccine may address this issue. Methods : In Niger three doses of a bivalent meningococcal A + C diphtheria-toxoid-conjugated vaccine (MenD), containing 1, 4 or 16 micrometer grams of each polysaccharide per dose, administered at 6, 10 and 14 weeks of age, were compared with #Haemophilus influenzae$ type b-tetanus toxoid-conjugated (PRP-T) vaccine given with the same schedule or with a meningococcal A + C polysacharide vaccine (MenPS) given at 10 and 14 weeks of age. One blood sample was taken at the time of enrollment (6 weeks of age) and another was taken 4 weeks after the primary series. Results : all doses of MenD were well-tolerated. After the primary series a higher proportion of infants had detectable serum bactericidal activity against serogroup A for each dose of MenD (from 94% to 100%) than for MenPS (31%) or #H. influenzae$ type b-tetanus toxoid-conjuugated vaccine (18.9%) ; P is less than or equal to 0.05. Significant differences were also observed for serogroup C MenD 4 micrometer grams or MenD 16 micrometer grams (100%) vs. MenPS (69.7%) or #Haemophilus influenzae$ type b-tetanus toxoid-conjugated vaccine (24.3%) ; P is less than or equal to 0.05. When MenPS vaccine was given to 11-month children, the immune response measured by both enzyme-linked immunosorbent assay and serum bactericidal assay was greater in those previously immunized with MenD than in those immunized with MenPS vaccine. Conclusion : MenD was safe among infants in Niger, and immunization led to significantly greater functional antibody activity than with MenPS. The 4-micrometer gram dose of MedD for both the A and C serogroups has been selected for further studies. (Résumé d'auteur)</abstract>
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