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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%">Toure Balde, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Perlaza, B.L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sauzet, J.P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ndiaye, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Aribot, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Tall, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Sokhna, Cheikh</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Rogier, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Corradin, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Roussilhon, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Druilhe, P.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Evidence for multiple B- and T-cell epitopes in Plasmodium falciparum liver-stage antigen 3</title>
        <secondary-title>Infection and Immunity</secondary-title>
      </titles>
      <pages>1189-1196</pages>
      <dates>
        <year>2009</year>
      </dates>
      <call-num>PAR00003353</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Infection and Immunity</full-title>
      </periodical>
      <isbn>0019-9567</isbn>
      <accession-num>ISI:000263416700030</accession-num>
      <number>3</number>
      <electronic-resource-num>10.1128/iai.00780-07</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/PAR00003353</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2023-02/010087124.pdf</url>
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      <volume>77</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Liver-stage antigen 3 (LSA-3) is a new vaccine candidate that can induce protection against Plasmodium falciparum sporozoite challenge. Using a series of long synthetic peptides (LSP) encompassing most of the 210-kDa LSA-3 protein, a study of the antigenicity of this protein was carried out in 203 inhabitants from the villages of Dielmo (n=143) and Ndiop (n=60) in Senegal (the level of malaria transmission differs in these two villages). Lymphocyte responses to each individual LSA-3 peptide were recorded, some at high prevalences (up to 43%). Antibodies were also detected to each of the 20 peptides, many at high prevalence (up to 84% of responders), and were directed to both nonrepeat and repeat regions. Immune responses to LSA-3 were detectable even in individuals of less than 5 years of age and increased with age and hence exposure to malaria, although they were not directly related to the level of malaria transmission. Thus, several valuable T- and B-cell epitopes were characterized all along the LSA-3 protein, supporting the antigenicity of this P. falciparum vaccine candidate. Finally, antibodies specific for peptide LSP10 located in a nonrepeat region of LSA-3 were found significantly associated with a lower risk of malaria attack over 1 year of daily clinical follow-up in children between the ages of 7 and 15 years, but not in older individuals.</abstract>
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      <custom1>UR198</custom1>
      <custom7>Sénégal</custom7>
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