PMID- 15472297 OWN - NLM STAT- MEDLINE DCOM- 20041223 LR - 20191210 IS - 0095-1137 (Print) IS - 1098-660X (Electronic) IS - 0095-1137 (Linking) VI - 42 IP - 10 DP - 2004 Oct TI - Detection of Paracoccidioides brasiliensis gp70 circulating antigen and follow-up of patients undergoing antimycotic therapy. PG - 4480-6 AB - Paracoccidioidomycosis (PCM), one of the most important systemic mycoses in Central and South America, is caused by the dimorphic fungus Paracoccidioides brasiliensis and has a high prevalence in Brazil. Glycoproteins of 43 and 70 kDa are the main antigenic compounds of P. brasiliensis and are recognized by Western blotting by 100 and 96% of PCM patient sera, respectively. In the present study, an inhibition enzyme-linked immunosorbent assay (ELISA) was used to detect gp70 in different biological samples from patients with PCM. gp70 was detected in 98.76% of 81 serum samples, with an average concentration of 8.19 microg/ml. The test was positive for 100% of the patients with the acute and chronic unifocal forms of PCM and 98.43% of the patients with the multifocal chronic form, with average concentrations of 11.86, 4.83, and 7.87 microg/ml, respectively. Bronchoalveolar lavage fluid from 23 patients with pulmonary unifocal PCM and 14 samples of cerebrospinal fluid from patients with neurological PCM were also tested for gp70 detection, with the test showing 100% sensitivity and 100% specificity, with mean gp70 concentrations of 7.5 and 6.78 microg/ml, respectively. To investigate the potential of gp70 detection by inhibition ELISA for the follow-up of PCM patients during antimycotic therapy with itraconazole (ITZ), the sera of 23 patients presenting with the chronic multifocal form of PCM were monitored at regular intervals of 1 month for 12 months. The results showed a decrease in circulating gp70 levels during treatment which paralleled the reduction in anti-P. brasiliensis antibody levels. The detection of P. brasiliensis gp70 from the biological fluids of patients suspected of having PCM proved to be a promising method for diagnosing infection and evaluating the efficacy of ITZ treatment. FAU - da Silva, Silvia Helena Marques AU - da Silva SH AD - Department of Microbiology, Immunology and Parasitology, Federal University of Sao Paulo, Sao Paulo, SP, Brazil. FAU - Grosso, Daniela de Mattos AU - Grosso Dde M FAU - Lopes, Jose Daniel AU - Lopes JD FAU - Colombo, Arnaldo Lopes AU - Colombo AL FAU - Blotta, Maria Heloisa Souza Lima AU - Blotta MH FAU - Queiroz-Telles, Flavio AU - Queiroz-Telles F FAU - de Camargo, Zoilo Pires AU - de Camargo ZP LA - eng PT - Evaluation Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Clin Microbiol JT - Journal of clinical microbiology JID - 7505564 RN - 0 (Antifungal Agents) RN - 0 (Antigens, Fungal) RN - 304NUG5GF4 (Itraconazole) SB - IM MH - Adolescent MH - Antifungal Agents/*therapeutic use MH - Antigens, Fungal/*blood MH - Enzyme-Linked Immunosorbent Assay/methods MH - Female MH - Humans MH - Itraconazole/*therapeutic use MH - Male MH - Middle Aged MH - Paracoccidioides/immunology/*isolation & purification MH - Paracoccidioidomycosis/*diagnosis/*drug therapy/microbiology PMC - PMC522319 EDAT- 2004/10/09 09:00 MHDA- 2004/12/24 09:00 PMCR- 2004/10/01 CRDT- 2004/10/09 09:00 PHST- 2004/10/09 09:00 [pubmed] PHST- 2004/12/24 09:00 [medline] PHST- 2004/10/09 09:00 [entrez] PHST- 2004/10/01 00:00 [pmc-release] AID - 42/10/4480 [pii] AID - 0504-04 [pii] AID - 10.1128/JCM.42.10.4480-4486.2004 [doi] PST - ppublish SO - J Clin Microbiol. 2004 Oct;42(10):4480-6. doi: 10.1128/JCM.42.10.4480-4486.2004.