Role of recombinant Histoplasma capsulatum 100‐kilodalton antigen in the diagnosis of histoplasmosis among HIV/AIDS patients: Antigenuria and antibodies detection

Author:

Toscanini María A.12,Laboccetta Carolina Rodríguez12,Videla Garrido Agustín2,Posse Gladys B.3,Capece Paula3,Valdez Ruth M.4,Chacón Yone A.4,González Maglio Daniel56ORCID,Nusblat Alejandro D.1,Cuestas María L.2ORCID

Affiliation:

1. Facultad de Farmacia y Bioquímica, Instituto de Nanobiotecnología (NANOBIOTEC) Universidad de Buenos Aires Buenos Aires Argentina

2. CONICET, Instituto de Investigaciones en Microbiología y Parasitología Médica (IMPaM) Universidad de Buenos Aires Buenos Aires Argentina

3. Laboratorio de Micología Hospital Nacional Profesor Alejandro Posadas Buenos Aires Argentina

4. Laboratorio de Micología, Hospital Señor del Milagro de Salta Salta Argentina

5. Facultad de Farmacia y Bioquímica, Cátedra de Inmunología Universidad de Buenos Aires Buenos Aires Argentina

6. Instituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET‐Universidad de Buenos Aires Buenos Aires Argentina

Abstract

AbstractBackgroundDiagnosing progressive disseminated histoplasmosis (PDH) is still challenging in many countries where this disease is highly endemic. Definitive diagnosis is established by culture and/or by cytology/histopathology but both procedures have limited sensitivity and cultures are time‐consuming. Antibodies detection by immunodiffusion has a low sensitivity in immunocompromised individuals. Commercially available antigen detection assays have high sensitivity in PDH cases; however, they are expensive and only performed in few laboratories.AimsTo describe the potential use of a novel ELISA for antibodies testing and a dot blot assay for antigen testing for diagnosing PDH using the recombinant 100 kDa protein of Histoplasma capsulatum (Hcp100) and their polyclonal antibodies as novel reagents, respectively.MethodsSerum and urine samples from a cohort of patients with HIV/AIDS and proven PDH were studied for the detection of anti‐Hcp100 antibodies by ELISA and Hcp100 antigen by dot blot, respectively. Sensitivity, specificity and cross‐reactions with other diseases were estimated for each assay and compared with those obtained using histoplasmin (HMN) as a reagent for antibodies detection by ELISA and immunodiffusion, and using a commercial antigenuria test.ResultsAntibodies detection by the Hcp100 ELISA demonstrated 78.6% sensitivity and 88.4% specificity, versus 85.7% sensitivity and 81.0% specificity for the HMN ELISA and 26.1% sensitivity and 100% specificity for the immunodiffusion assay. Antigen detection by the Hcp100 dot blot demonstrated 89.3% sensitivity and 97.0% specificity versus 82.1% sensitivity and 90.9% specificity for the commercial test.ConclusionThe immunoassays described herein based on Hcp100 would be a valuable screening tool for diagnosing PDH.

Funder

Agencia Nacional de Promoción Científica y Tecnológica

Publisher

Wiley

Subject

Infectious Diseases,Dermatology,General Medicine

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