<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Differential infectivity and immunopathology in murine experimental infections by two natural clones belonging to the Trypanosoma cruzi I lineage</dc:title>
  <dc:creator>/Garzon, Edwin</dc:creator>
  <dc:creator>/Genna, F.</dc:creator>
  <dc:creator>/Bosseno, Marie-France</dc:creator>
  <dc:creator>Simony La Fontaine, J.</dc:creator>
  <dc:creator>Radal, M.</dc:creator>
  <dc:creator>/S&#xE9;r&#xE9;no, Denis</dc:creator>
  <dc:creator>/Mathieu Daud&#xE9;, Fran&#xE7;oise</dc:creator>
  <dc:creator>/Ouaissi, Ali</dc:creator>
  <dc:creator>/Breni&#xE8;re, Simone Fr&#xE9;d&#xE9;rique</dc:creator>
  <dc:subject>Trypanosoma cruzi</dc:subject>
  <dc:subject>genotype</dc:subject>
  <dc:subject>immunopathology</dc:subject>
  <dc:subject>virulence</dc:subject>
  <dc:subject>mouse</dc:subject>
  <dc:description>Immunopathology of Chagas' disease in Balb/c mice infected with 2 Trypanosoma cruzi clones, belonging to the T. cruzi I lineage and presenting different in vitro virulence (P/209 ell &gt; SO34 c14) was compared. In the acute phase, evading mechanisms such as parasite-induced lymphocyte polyclonal activation and T cell immunosuppression were higher in mice infected with the clone giving a higher parasitaemia (P/209 c11). A similar increase of non-specific isotypes was observed in both infections with IgG2a prevalence. Interestingly, CD8+ cell hypercellularity and lymphocyte immunosuppression were observed during the chronic phase (245 days post-infection) in mice infected by the most virulent clone. In the same way, the parasite-specific antibody response was more intense in P/209 c11-infected mice over the acute phase. During the chronic phase this response remarkably dropped down in SO34 c14-infected mice exclusively. Finally, P/209 ell-infected mice presented a more severe inflammation and tissue damage in heart and quadriceps than SO34 c14-infected mice. This comparative study showed differences between the two clones: a higher virulence in vivo being clearly associated with a greater ability to induce evasion mechanisms and severe tissue damage.</dc:description>
  <dc:date>2005</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010041532</dc:identifier>
  <dc:identifier>fdi:010041532</dc:identifier>
  <dc:identifier>Garzon Edwin, Genna F., Bosseno Marie-France, Simony La Fontaine J., Radal M., S&#xE9;r&#xE9;no Denis, Mathieu Daud&#xE9; Fran&#xE7;oise, Ouaissi Ali, Breni&#xE8;re Simone Fr&#xE9;d&#xE9;rique. Differential infectivity and immunopathology in murine experimental infections by two natural clones belonging to the Trypanosoma cruzi I lineage. 2005, 131 (Part 1),  109-119</dc:identifier>
  <dc:language>EN</dc:language>
</oai_dc:dc>
