Marques da Silva Silvia Helena, Colombo Arnaldo Lopes, Blotta Maria Heloisa Souza Lima, Lopes José Daniel, Queiroz-Telles Flávio, Pires de Camargo Zoilo
Department of Microbiology, Immunology and Parasitology, Federal University of São Paulo, São Paulo, Brazil.
J Clin Microbiol. 2003 Aug;41(8):3675-80. doi: 10.1128/JCM.41.8.3675-3680.2003.
Paracoccidioidomycosis (PCM) is an important systemic fungal disease, particularly among individuals living and working in rural areas of endemicity in Latin America, who, without antifungal therapy, may develop fatal acute or chronic infection. For such patients, the detection of antibody responses by immunodiffusion is of limited value due to false-negative results. In contrast, the detection of Paracoccidioides brasiliensis gp43 circulating antigen may represent a more practical approach to the rapid diagnosis of the disease. Accordingly, an inhibition enzyme-linked immunosorbent assay (inh-ELISA) was developed for the detection of a 43-kDa P. brasiliensis-specific epitope incorporating a species-specific murine monoclonal antibody. With sera from patients with acute and chronic forms of the disease (n = 81), the overall sensitivity of the test was found to be 95.1%, while specificity was found to be 97.5% compared to that with normal human sera from blood donors (n = 93) and sera from patients with other chronic fungal infections (histoplasmosis [n = 33] and cryptococcosis [n = 20]). The inh-ELISA detected circulating antigen in 100% of patients with the acute form of PCM and in 95.31 and 100% of patients with the chronic multifocal and unifocal forms of PCM according to the patient's clinical presentation. Cerebrospinal fluid from 14 patients with neuroparacoccidioidomycosis and 13 samples of bronchoalveolar lavage fluid from patients with pulmonary unifocal PCM were also tested for gp43 detection, with the test showing 100% sensitivity and specificity. This novel, highly specific inh-ELISA represents a significant addition to the existing tests for the diagnosis of PCM.
副球孢子菌病(PCM)是一种重要的系统性真菌病,在拉丁美洲地方性流行地区生活和工作的人群中尤为常见,这些人若不接受抗真菌治疗,可能会发展为致命的急性或慢性感染。对于此类患者,由于假阴性结果,通过免疫扩散检测抗体反应的价值有限。相比之下,检测巴西副球孢子菌gp43循环抗原可能是一种更实用的疾病快速诊断方法。因此,开发了一种抑制酶联免疫吸附测定(inh-ELISA),用于检测包含物种特异性鼠单克隆抗体的43 kDa巴西副球孢子菌特异性表位。在急性和慢性疾病患者的血清(n = 81)中,该检测的总体敏感性为95.1%,而与来自献血者的正常人血清(n = 93)以及其他慢性真菌感染(组织胞浆菌病[n = 33]和隐球菌病[n = 20])患者的血清相比,特异性为97.5%。根据患者的临床表现,inh-ELISA在100%的急性PCM患者以及95.31%和100%的慢性多灶性和单灶性PCM患者中检测到循环抗原。还对14例神经副球孢子菌病患者的脑脊液和13例肺单灶性PCM患者的支气管肺泡灌洗液样本进行了gp43检测,该检测显示出100%的敏感性和特异性。这种新型的、高度特异性的inh-ELISA是PCM诊断现有检测方法的一项重要补充。