Screening and evaluation of Mycobacterium tuberculosis diagnostic antigens
Autor: | Zhen Wang, Hang Yang, Zhongchen Ma, Chuangfu Chen, Jinke He, Qian Zhang, Xiang Ji, Yong Wang |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Microbiology (medical) Indirect elisa medicine.medical_specialty Tuberculosis 030106 microbiology Enzyme-Linked Immunosorbent Assay Disease DIAGNOSTIC ANTIGENS Mycobacterium tuberculosis 03 medical and health sciences 0302 clinical medicine Medical microbiology Antigen Tuberculosis Multidrug-Resistant medicine Humans 030212 general & internal medicine Antigens Bacterial biology business.industry General Medicine biology.organism_classification medicine.disease Antibodies Bacterial Infectious Diseases Immunology biology.protein Antibody business |
Zdroj: | European Journal of Clinical Microbiology & Infectious Diseases. 39:1959-1970 |
ISSN: | 1435-4373 0934-9723 |
Popis: | In recent years, the prevalence of tuberculosis worldwide has increased, and with it, the number of drug-resistant tuberculosis strains. This has brought new challenges towards prevention and control of the disease. Therefore, it is urgent to find reliable and rapid diagnostic methods for tuberculosis in general, and for the drug-resistant forms of the disease. To this aim, we assessed 17 tuberculosis-specific protein candidates for the detection of tuberculosis-specific antibodies. First, we established an indirect ELISA method to detect anti-Mycobacterium tuberculosis IgM and IgG. We tested 453 sera and analyzed the efficacy of the protein candidates for diagnosis of tuberculosis. Next, we screened antigens rich in T cell epitopes for their ability to induce high levels of IFN-γ, in order to define their suitability does develop detection tests based on IFN-γ release assay (IGRAs). The antigens CFP-10, PPE57, 38kDa, and Rv3807 showed higher diagnostic potential for the detection of anti-tuberculosis IgM, whereas PPE57, Ag85B, CFP-10, Rv0220, and 38kDa antigens performed better for anti-tuberculosis IgG detection. Worth noting is that CFP-10, 38kDa, and PPE57 detected efficiently both IgM and IgG. Rv1987, Rv3807, PPE57, Rv0220, and MPT64 proteins alone and combinations of Rv1987 + Rv3807, 16kDa + Rv0220, and MPT64 + Rv1986 tested in IGRAs displayed a good correlation with the positive control constituted by a cocktail of ESAT-6 + CFP-10 + TB7.7 (ECT), known for their stimulating properties (r > 0.5, p |
Databáze: | OpenAIRE |
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