Abstract
Immunoblot assays showed that mycobacterial fibronectin-binding antigens are important targets of the humoral immune response in tuberculosis and leprosy. Using culture filtrate antigens of Mycobacterium tuberculosis, strong reactivity with the fibronectin-binding of 30-31 kD (Fn 30-31) was demonstrated in 55.9% of tuberculosis sera and in 56.5% of lepromatous leprosy sera. Sera from patients with tuberculoid leprosy and control sera gave very weak binding. Reactivity of tuberculosis and lepromatous leprosy sera with the fibronectin-binding antigen of 58-60 kD (Fn 58-60) was less conspicuous. The ability to react with fibronectin of the antigens of 58-60 and 30-31 kD was demonstrated by parallel labelling with a fibronectin-biotin conjugate. Fn 30-31 was purified to homogeneity by a two-step procedure and used for ELISA. Positive titres were found in 63% out of 65 tuberculosis sera and in 60.5% out of 43 lepromatous leprosy sera. Antibody titres in lepromatous leprosy sera were higher than in tuberculosis sera. Our observations indicate indirectly that M. leprae possess a highly immunogenic molecule homologous to M. tuberculosis Fn 30-31, which elicits a high antibody response in lepromatous leprosy but not in tuberculoid leprosy. In this investigation, direct evidence for the presence of this antigen in M. leprae was obtained by immunochemistry of lepromatous leprosy lesions with a monospecific antibody raised against M. tuberculosis Fn 30-31.
MeSH Terms
Antibodies, Bacterial/analysis
Antigens, Bacterial/immunology
Electrophoresis, Polyacrylamide Gel
Enzyme-Linked Immunosorbent Assay
Epitopes/immunology
Fibronectins/immunology
Humans
Immunoblotting
Immunoenzyme Techniques
Leprosy, Lepromatous/immunology,pathology
Leprosy, Tuberculoid/immunology,pathology
Molecular Weight
Mycobacterium leprae/immunology
Mycobacterium tuberculosis/immunology
Tuberculosis, Pulmonary/immunology
Chemicals
Antibodies, Bacterial
Antigens, Bacterial
Epitopes
Fibronectins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Espitia C
Departamento de Inmunología, Universidad Nacional Autónoma de México, D.F.
Sciutto E
Bottasso O
González-Amaro R
Hernández-Pando R
Mancilla R
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