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:99-1</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">99-1</td><td><b>Evaluation of the peripheral T lymphocytes subsets in paracoccidioidomycosis-patients at different moments during antifungal therapy</b></td></tr><tr><td valign=top>Authors:</td><td><u>James Venturini </u> (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Marjorie de Assis Golim (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Tatiane Fernanda Sylvestre (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Daniela Vanessa Moris (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Ricardo Souza Cavalcante (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Valéria Alves Silva (FMB-UNESP - Faculdade de Medicina de Botucatu) ; Maria Sueli Arruda (FC-UNESP - Faculdade de Ciências) ; Rinaldo Poncio Mendes (FMB-UNESP - Faculdade de Medicina de Botucatu) </td></tr></table><p align=justify><b><font size=2>Abstract</font></b><p align=justify class=tres><font size=2><b>Introduction.</b> Recovery of the cell-mediated immunity is fundamental for the discontinuation of the antifungal therapy in paracoccidioidomycosis-patients (PCM-p). This study aims to quantify the T lymphocytes subsets of patients before, during and after treatment. <b>Patients and methods.</b> A total of 122 PCM-p, classified as to Mendes et al. (1994), were studied: 32 with acute/subacute form-AF (29 severe-AFs and 3 moderate) and 90 with chronic form-CF (27 severe-CFs, 54 moderate-CFm and 9 mild). PCM-p were evaluated at different moments: M1- before treatment (n=16); M2- under treatment, symptomatic (n=24); M3- asymptomatic, under treatment, positive DID (n=28); M4- asymptomatic, under treatment, negative DID (n=36); M5- asymptomatic, no-treatment, negative DID, within 2-year follow-up (n=44); M6- asymptomatic, no-treatment, negative DID, after 2-year discontinuation therapy (n=42). T lymphocytes subsets counts in 451 blood samples were immunolabelled using antibodies anti-CD3/CD4/CD8 (TriTEST kit-BD<sup>TM</sup>) and analysed by flow cytometry; results were expressed as TCD3+, TCD4+, TCD8+ cells counts/mm<sup>3</sup> and the TCD4+/TCD8+ ratio. The control group was constituted by 436 healthy individuals. Averages were compared by unpaired T test and ANOVA followed by Tukey test. Significance was set up at p<0.05. <b>Results.</b> 1. <u>CD3 (normal range values: 755-2012)</u> - AF vs. CF - M1: AF=1314; CF=1798, p=0.04; M2: AF=1318; CF=1924, p=0.05; M3: AF=1257; CF=1935, p=0.11; M4: AF=1475; CF=1686, p=0.35; M5: AF=1408; CF=1609, p=0.44; M6: AF=1226; CF=1660, p=0.15. 2. <u>CD4 (437-1209)</u> - AF vs. CF - M1: AF=849; CF=1144, p=0.14; M2: AF=836; CF=1245, p=0.03; M3: AF=798; CF=1173, p=0.16; M4: AF=842; CF=1026, p=0.17; M5: AF=868; CF=1064, p=0.27; M6: AF=763; CF=1126, p=0.08. 3. <u>CD8 (180-774)</u> - AF vs. CF - M1: AF=406; CF=564, p=0.07; M2: AF=393; CF=617, p=0.11; M3: AF=412; CF=696, p=0.11; M4: AF=514; CF=586, p=0.49; M5: AF=470; CF=492, p=0.80; M6: AF=419; CF=474, p=0.61. 4. <u>CD4/CD8 ratio (1.0-3.1)</u> - AF vs. CF - M1: AF=2.2; CF=2.5, p=0.64; M2: AF=2.1; CF=2.3, p=0.63; M3: AF=2.1; CF=2.0, p=0.81; M4: AF=2.0; CF=1.9, p=0.76; M5: AF=2.1; CF=2.4, p=0.46; M6: AF=1.9; CF=2.8, p=0.17. <b>Conclusions.</b> CD3 was higher in CF than in AF before treatment but within the normal limits. During the follow-up AF showed no variation and CF a tendency to decrease CD3 and CD8 and a decrease of CD4 in CFm after treatment.</font></p><br><b>Keyword: </b>&nbsp;T lymphocytes subsets, antifungal therapy, paracoccidioidomycosis-patients</td></tr></table></tr></td></table></body></html>