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    <title>Cuisinier, A.M.</title>
    <link>http://repub.eur.nl/res/aut/10203/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Vaccination with experimental feline immunodeficiency virus vaccines, based on autologous infected cells, elicits enhancement of homologous challenge infection. (Article)</title>
      <link>http://repub.eur.nl/res/pub/3664/</link>
      <pubDate>1999-01-01T00:00:00Z</pubDate>
      <description>Cats were vaccinated with fixed autologous feline immunodeficiency virus (FIV)-infected cells in order to present viral proteins to the immune system of individual cats in an MHC-matched fashion. Upon vaccination, a humoral response against Gag was induced. Furthermore, virus-neutralizing antibodies were detected in a Crandell feline kidney cell-based neutralization assay, but not in a neutralization assay based on primary peripheral blood mononuclear cells. Despite the induction of these FIV-specific responses, vaccinated cats were not protected. Instead, accelerated virus replication was found, an observation similar to what previous experiments using other vaccine candidates have shown. Here, the results of the present study are discussed in the light of enhancement of lentivirus infections as a complicating factor in lentivirus vaccine development.</description>
    </item> <item>
      <title>Vaccination with experimental feline immunodeficiency virus vaccines, based on autologous infected cells, elicits enhancement of homologous challenge infection (Article)</title>
      <link>http://repub.eur.nl/res/pub/8469/</link>
      <pubDate>1999-01-01T00:00:00Z</pubDate>
      <description>Cats were vaccinated with fixed autologous feline immunodeficiency virus
      (FIV)-infected cells in order to present viral proteins to the immune
      system of individual cats in an MHC-matched fashion. Upon vaccination, a
      humoral response against Gag was induced. Furthermore, virus-neutralizing
      antibodies were detected in a Crandell feline kidney cell-based
      neutralization assay, but not in a neutralization assay based on primary
      peripheral blood mononuclear cells. Despite the induction of these
      FIV-specific responses, vaccinated cats were not protected. Instead,
      accelerated virus replication was found, an observation similar to what
      previous experiments using other vaccine candidates have shown. Here, the
      results of the present study are discussed in the light of enhancement of
      lentivirus infections as a complicating factor in lentivirus vaccine
      development.</description>
    </item>
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