ÿþ<HTML><HEAD><TITLE>XI International Meeting on Paracoccidioidomycosis</TITLE><link rel=STYLESHEET type=text/css href=css.css></HEAD><BODY aLink=#ff0000 bgColor=#FFFFFF leftMargin=0 link=#000000 text=#000000 topMargin=0 vLink=#000000 marginheight=0 marginwidth=0><table align=center width=700 cellpadding=0 cellspacing=0><tr><td align=left bgcolor=#cccccc valign=top width=550><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=3><font size=1>XI International Meeting on Paracoccidioidomycosis</font></font></strong><font face=Verdana size=1><b><br></b></font><font face=Verdana, Arial,Helvetica, sans-serif size=1><strong> </strong></font></font></td><td align=right bgcolor=#cccccc valign=top width=150><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=1><font size=1>Resume:117-1</font></em></font></strong></font></td></tr><tr><td colspan=2><br><br><table align=center width=700><tr><td><b>Poster (Painel)</b><br><table width="100%"><tr><td width="60">117-1</td><td><b>Paracoccidioides brasiliensis-induced migration of respiratory dendritic cells and subsequent antigen presentation in the lung draining lymph node</b></td></tr><tr><td valign=top>Authors:</td><td><u>Suelen Silvana dos Santos </u> (USP - Universidade de São Paulo) ; Karen Spadari Ferreira (UNIFESP - Universidade Federal de São Paulo - Campus Diadema) ; Sandro Rogério de Almeida (USP - Universidade de São Paulo) </td></tr></table><p align=justify><b><font size=2>Abstract</font></b><p align=justify class=tres><font size=2>Paracoccidioidomycosis (PCM) is a systemic mycosis caused by <i> Paracoccidioides brasiliensis (Pb)</i>, which mainly affects the lungs. They are one of the few organs that are in constant and intense interaction with the environment and the immune system. The great challenge for the pulmonary immune system is to discriminate what is harmful and react accordingly. Dendritic cells (DCs) are "professionals" antigen-presenting cells and they can do the antigen processing. They can also do the presentation of peptides to T lymphocytes and are ideal for maintaining this delicate balance between tolerance and an effector immune response. Knowing the importance of these cells in the immune system and that the infection by <i>(Pb)</i> preferentially attacks the lungs, cells from bronchoalveolar lavage (BAL), after experimental infection with yeasts of <i>(Pb)</i>, were analyzed. We observed a significant increase of DCs in BAL after 24 hours of intratracheal infection with yeast cells of <i>(Pb)</i>. The characterization of these cells showed that DCs expressed CD11c, MHC-II and DEC205. In order to verify the ability of migration of DCs, they were differentiated from bone marrow cells and pulsed with yeasts of <i>(Pb)</i>, they were also labeled with CFSE and injected intratracheally into mice. As a negative control, we used PBS and DCs that were not pulsed with the fungus. The results showed that after 12 hours of infection, the DCs (CFSE+/CD11c+), migrated to the thoracic lymph nodes. However, the quantity of these cells decreases slightly after 24 hours of infection. Furthermore, we observed no DCs in regional lymph nodes when we analyzed the control groups. Thus, the lung cells were also labeled in vivo by injecting the CFSE dye intratracheally with yeasts of <i>(Pb)</i>. We found that after 12 hours, pulmonary DCs of the animals infected with the fungus migrated to regional lymph nodes. These results indicate that the fungus <i>Paracoccidioides brasiliensis</i> was able to activate DCs, inducing their migration to regional lymph nodes, and inducing a response in that organ by T cells as evidenced by preferential production of IL-10.</font></p><br><b>Keyword: </b>&nbsp;Paracoccidioidomycosis, Paracoccidioides brasiliensis, Dendritic cells</td></tr></table></tr></td></table></body></html>