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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="bold" font="default" size="100%">Petitdidier, Elodie</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Pagniez, Julie</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Pissarra, J.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Holzmuller, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Papierok, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Vincendeau, P.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Lemesre, Jean-Loup</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Bras Goncalves, Rachel</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Peptide-based vaccine successfully induces protective immunity against canine visceral leishmaniasis</title>
        <secondary-title>NPJ Vaccines</secondary-title>
      </titles>
      <pages>art. 49 [9 ]</pages>
      <dates>
        <year>2019</year>
      </dates>
      <call-num>fdi:010077468</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>NPJ Vaccines</full-title>
      </periodical>
      <accession-num>ISI:000502998700001</accession-num>
      <electronic-resource-num>10.1038/s41541-019-0144-2</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010077468</url>
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          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers20-01/010077468.pdf</url>
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      <volume>4</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Dogs are the main reservoir of zoonotic visceral leishmaniasis. Vaccination is a promising approach to help control leishmaniasis and to interrupt transmission of the Leishmania parasite. The promastigote surface antigen (PSA) is a highly immunogenic component of Leishmania excretory/secretory products. A vaccine based on three peptides derived from the carboxy-terminal part of Leishmania amazonensis PSA and conserved among Leishmania species, formulated with QA-21 as adjuvant, was tested on naive Beagle dogs in a preclinical trial. Four months after the full course of vaccination, dogs were experimentally infected with Leishmania infantum promastigotes. Immunization of dogs with peptide-based vaccine conferred immunity against experimental infection with L. infantum. Evidence for macrophage nitric oxide production and anti-leishmanial activity associated with IFN-y production by lymphocytes was only found in the vaccinated group. An increase in specific IgG2 antibodies was also measured in vaccinated dogs from 2 months after immunization. Additionally, after challenge with L. infantum, the parasite burden was significantly lower in vaccinated dogs than in the control group. These data strongly suggest that this peptide-based vaccine candidate generated cross-protection against zoonotic leishmaniasis by inducing a Th1-type immune response associated with production of specific IgG2 antibodies. This preclinical trial including a peptide-based vaccine against leishmaniasis clearly demonstrates effective protection in a natural host. This approach deserves further investigation to enhance the immunogenicity of the peptides and to consider the possible engineering of a vaccine targeting several Leishmania species.</abstract>
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      <custom1>UR177</custom1>
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