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
{"title":"\"Reactivity of Cryptococcal Lateral Flow Assay in Aspergillosis, Histoplasmosis, Paracoccidioidomycosis, Candidiasis, Trichosporonosis, Bacterial and Viral infections\".","authors":"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","doi":"10.1093/mmy/myaf068","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18586,"journal":{"name":"Medical mycology","volume":" ","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical mycology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/mmy/myaf068","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
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.
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.