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:137-6</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">137-6</td><td><b>Prevalence of blood group antigens in paracoccidioidomycosis-patients. Preliminary results.</b></td></tr><tr><td valign=top>Authors:</td><td>Jessica Enéas Fulfaro (FMB - UNESP - FACULDADE DE MEDICINA DE BOTUCATU - UNESP) ; Elenice Deffune (HB - HEMOCENTRO DE BOTUCATUFMB - UNESP - FACULDADE DE MEDICINA DE BOTUCATU - UNESP) ; <u>Rinaldo Poncio Mendes </u> (FMB - UNESP - FACULDADE DE MEDICINA DE BOTUCATU - UNESP) </td></tr></table><p align=justify><b><font size=2>Abstract</font></b><p align=justify class=tres><font size=2><b>Introduction.</b> Paracoccidioidomycosis (PCM), systemic mycosis with antigen-dependent immunosupression, has not been evaluated as to genetic factors of susceptibility and resistance. Objectives. This study investigated the prevalence of different red blood cells surface antigens in PCM-patients as to clinical forms. <b>Patients and Methods.</b> A total of 105 patients with PCM confirmed by the identification of typical <i>Paracoccidioides brasiliensis</i> yeast forms in different clinical materials and/or anti-<i>P. brasiliensis</i> antibodies demonstrated by the double agar gel immunodiffusion test, in any phase of the disease, were enrolled in this study. Co-morbidities, except alcohol intake and smoking habit, were exclusion criteria. Clinical forms and severity were classified as to Mendes et al. (1994). Three groups were constituted: G1- 21 patients / acute/subacute form (AF); G2- 84 patients / chronic form (CF); G3 - control group - 157 donors from Botucatu Blood Center . ABO, MNS, Rh, Kell, Lewis, Duffy and Kidd were the blood group systems evaluated by using the ID-Micro-Typing SystemTM (ID-MTS) Gel TestTM. Frequencies were compared by Fisher s exact test or chi-square test; significance was set up at p &#8804; 0.05. <b>Results.</b> The frequencies of the antigens in each different blood group systems will be presented in percentage in PCM-patients as a whole (G1+G2), in G1, G2 and G3: a) ABO system: O (52.4, 57.1, 51.2, 49.0), A (35.0, 38.1, 34.1, 36.5), B (11.7, 4.8, 13.4, 10.9), AB (1.0, 0.0, 1.2, 3.6); b) Rh system: D (89.3, 90.5, 89.0, 82.2); C (66.3, 57.1, 68.7, 63.7); c (76.2, 81.0, 75.0, 73.9); E (31.4., 42.9, 28.6, 30.0); e (96.2, 85.7, 98.8, 94.3); c) Duffy system: Fya (64.0, 50.0, 64.6, 64.3); Fyb (41.3, 26.7, 45.0, 71.3); d) Kidd system: Jka (49.3, 53.8, 48.2, 70.7); Jkb (66.7, 50.0, 68.8, 70.0); e) MNS system: M (75.0, 80.0, 73.8, 76.4); N (57.7, 53.8, 58.5, 68.8); S (43.6, 35.3, 45.5, 47.2); s (92.3, 95.0, 91.7, 94.9); f) Lewis system: Lea (8.0, 5.0, 8.8, 15.3); Leb (37.2, 35.7, 37.5, 66.3); g) Kell system: K (8.7, 10.0, 8.4, 18.5). A lower frequency of Fyb, K and Leb was observed in PCM-p [<b><i>p</b></i> < 0.05]. As to clinical form, <b> e </b> antigen (Rh system) showed lower frequency in the AF (85.7%) than in the CF (98.8%) [<b><i>p</b></i> = 0.02]. <b>Conclusion.</b> We are now studying if these findings could be a risk factor for PCM or if they influence its clinical expression.</font></p><br><b>Keyword: </b>&nbsp;paracoccidioidomycosis, blood group antigens, phenotyping</td></tr></table></tr></td></table></body></html>