"Reactivity of Cryptococcal Lateral Flow Assay in Aspergillosis, Histoplasmosis, Paracoccidioidomycosis, Candidiasis, Trichosporonosis, Bacterial and Viral infections".

IF 2.3 3区 医学 Q3 INFECTIOUS DISEASES
Edite Hatsumi Yamashiro-Kanashiro, Kelly Aparecida Kanunfre, Evanthia Vetos Mimicos, Vera Lúcia Teixeira de Freitas, Mussya Cisotto Rocha, Érika Yoshie Shimoda Nakanishi, Márcia Eiko Miyachi, Marjorie Vieira Batista, Roberto Martinez, Marcelo Nobrega Litvoc, Nairo Massakazu Sumita, Cláudia de Abreu Fonseca, Hélio Gomes Rodrigues, Eduardo Ronner Lagonegro, Maria Aparecida Shikanai Yasuda
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引用次数: 0

Abstract

Considering the need for a rapid, sensitive, and specific test for the early diagnosis of cryptococcal meningitis in critical regions where lumbar puncture and culture are inaccessible, we analyzed the specificity of the Lateral Flow Assay for cryptococcal antigen (LFA) in 217 serum specimens. Group 1: 68 HIV-uninfected patients with paracoccidioidomycosis, histoplasmosis, aspergillosis, trichosporonosis and 21 with tuberculosis; Group 2: 149 patients with HIV infection, including seven with histoplasmosis, and one with aspergillosis, and Group 3 with 24 proven cryptococcosis patients. Cross-reactivity of cryptococcal mannans and polysaccharides secreted by Paracoccidioides brasiliensis, Histoplasma capsulatum, and Trichosporon spp has been described in vitro. However, only a few cases of positive LFA tests in aspergillosis, trichosporonosis, candidemia, and bacterial infections sera have been reported. We observed false-positive LFA in 2/29 aspergillosis specimens but not in other mycoses or tuberculosis. Among 149 HIV-infected patients, three specimens tested positive, two had cytomegalovirus infections, one of whom also had toxoplasmosis and the other, Kaposi's sarcoma; one patient had no opportunistic infections. We observed sensitivities of 0.933 (serum), 0.95 (CSF), and 1.0 (serum or CSF) for LFA, and for all negative controls (N = 217, serum), a specificity of 0.977 and a negative predictive value (NPV) of 0 938. The specificity and NPV were 0.964 and 0 791, respectively, for 55 patients with mycoses; and 0.98 and 0.912 for 149 HIV-infected patients. We confirmed LFA's high specificity and accuracy for the control groups. There were 6.89% of false-positive results for aspergillosis, and no false-positive results for paracoccidioidomycosis, histoplasmosis, tuberculosis, or other bacterial diseases.

隐球菌横向流动测定在曲霉病、组织胞浆菌病、副球孢子菌病、念珠菌病、毛孢丝虫病、细菌和病毒感染中的反应性。
考虑到在无法进行腰椎穿刺和培养的关键区域,需要一种快速、敏感和特异性的检测方法来早期诊断隐球菌性脑膜炎,我们分析了217份血清标本中隐球菌抗原(LFA)的侧流试验的特异性。第1组:68例未感染hiv的副球孢子菌病、组织胞浆菌病、曲霉病、三孢子菌病和21例结核病患者;第2组:149例HIV感染,其中组织胞浆菌病7例,曲霉病1例;第3组24例确诊隐球菌病。隐球菌甘露聚糖与巴西副球虫、荚膜组织浆体和trichosporonspp分泌的多糖在体外的交叉反应性进行了研究。然而,在曲霉病、毛孢菌病、念珠菌病和细菌感染血清中,只有少数LFA检测阳性的病例被报道。我们在2/29曲霉病标本中观察到LFA假阳性,但在其他真菌病或结核病标本中未见假阳性。149例hiv感染者中,3例标本检测呈阳性,2例巨细胞病毒感染,1例同时患有弓形虫病,另1例同时患有卡波西肉瘤;一名患者没有机会性感染。我们观察到LFA的敏感性为0.933(血清)、0.95(脑脊液)和1.0(血清或脑脊液),所有阴性对照(N = 217,血清)的特异性为0.977,阴性预测值(NPV)为0.938。55例真菌病患者特异性为0.964,NPV为0.791;149例hiv感染者分别为0.98和0.912。我们证实了LFA在对照组中的高特异性和准确性。曲霉病的假阳性结果为6.89%,副球孢子菌病、组织胞浆菌病、结核病或其他细菌性疾病的假阳性结果为零。
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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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