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Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis

Elimination of tuberculosis (TB) largely depends upon definitive rapid diagnosis and treatment. Widely used diagnostic tests do not qualify for use in a developing country due to lack of either desired accuracy or their cost. In the present study an enzyme-linked immunosorbent assay was used to eval...

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Autores principales: Kumar, Gavish, Dagur, Pradeep Kumar, Singh, Prashant Kumar, Shankar, Hari, Yadav, Virendra S., Katoch, Vishwa M., Bajaj, Bharat, Gupta, Rajesh, Sengupta, Utpal, Joshi, Beenu
Formato: Texto
Lenguaje:English
Publicado: SP Birkhäuser Verlag Basel 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816261/
https://www.ncbi.nlm.nih.gov/pubmed/20049651
http://dx.doi.org/10.1007/s00005-009-0055-4
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author Kumar, Gavish
Dagur, Pradeep Kumar
Singh, Prashant Kumar
Shankar, Hari
Yadav, Virendra S.
Katoch, Vishwa M.
Bajaj, Bharat
Gupta, Rajesh
Sengupta, Utpal
Joshi, Beenu
author_facet Kumar, Gavish
Dagur, Pradeep Kumar
Singh, Prashant Kumar
Shankar, Hari
Yadav, Virendra S.
Katoch, Vishwa M.
Bajaj, Bharat
Gupta, Rajesh
Sengupta, Utpal
Joshi, Beenu
author_sort Kumar, Gavish
collection PubMed
description Elimination of tuberculosis (TB) largely depends upon definitive rapid diagnosis and treatment. Widely used diagnostic tests do not qualify for use in a developing country due to lack of either desired accuracy or their cost. In the present study an enzyme-linked immunosorbent assay was used to evaluate the diagnostic potential of an immuno-dominant 30/32-kDa mycolyl transferase complex (Ag85 complex) and Mycobacterium tuberculosis-specific proteins (ESAT-6 and CFP-10) of the RD1 region. Higher sensitivity (84.1%) with Ag85 complex was observed compared with ESAT-6 (64.9%) and CFP-10 (66%), with almost similar specificity (Ag85: 85.2%, ESAT-6: 88.9%, CFP-10: 85.2%), whereas the individual components of Ag85 complex, i.e. Ag85A, Ag85B, and Ag85C, showed sensitivities of 44.6, 34, and 80.9% and specificities of 55.6, 74.1, and 40.7% respectively. A cocktail of Ag85 complex, ESAT-6, CFP-10, Ag85A, Ag85B, and Ag85C antigens also could not help in increasing either sensitivity (51.1%) or specificity (85.2%). Furthermore, immunoblot analysis using clinical isolates as well as a standard strain (H37Rv) of M. tuberculosis also showed strong reactivity of sera from TB patients to Ag85 complex and, to a lesser extent, also to ESAT-6. To conclude, use of Ag85 complex along with ESAT-6 and CFP-10 seems to be promising in minimizing the heterogeneous sero-responses of adult TB cases.
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spelling pubmed-28162612010-02-13 Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis Kumar, Gavish Dagur, Pradeep Kumar Singh, Prashant Kumar Shankar, Hari Yadav, Virendra S. Katoch, Vishwa M. Bajaj, Bharat Gupta, Rajesh Sengupta, Utpal Joshi, Beenu Arch Immunol Ther Exp (Warsz) Original Article Elimination of tuberculosis (TB) largely depends upon definitive rapid diagnosis and treatment. Widely used diagnostic tests do not qualify for use in a developing country due to lack of either desired accuracy or their cost. In the present study an enzyme-linked immunosorbent assay was used to evaluate the diagnostic potential of an immuno-dominant 30/32-kDa mycolyl transferase complex (Ag85 complex) and Mycobacterium tuberculosis-specific proteins (ESAT-6 and CFP-10) of the RD1 region. Higher sensitivity (84.1%) with Ag85 complex was observed compared with ESAT-6 (64.9%) and CFP-10 (66%), with almost similar specificity (Ag85: 85.2%, ESAT-6: 88.9%, CFP-10: 85.2%), whereas the individual components of Ag85 complex, i.e. Ag85A, Ag85B, and Ag85C, showed sensitivities of 44.6, 34, and 80.9% and specificities of 55.6, 74.1, and 40.7% respectively. A cocktail of Ag85 complex, ESAT-6, CFP-10, Ag85A, Ag85B, and Ag85C antigens also could not help in increasing either sensitivity (51.1%) or specificity (85.2%). Furthermore, immunoblot analysis using clinical isolates as well as a standard strain (H37Rv) of M. tuberculosis also showed strong reactivity of sera from TB patients to Ag85 complex and, to a lesser extent, also to ESAT-6. To conclude, use of Ag85 complex along with ESAT-6 and CFP-10 seems to be promising in minimizing the heterogeneous sero-responses of adult TB cases. SP Birkhäuser Verlag Basel 2010-01-05 2010-02 /pmc/articles/PMC2816261/ /pubmed/20049651 http://dx.doi.org/10.1007/s00005-009-0055-4 Text en © L. Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland 2010
spellingShingle Original Article
Kumar, Gavish
Dagur, Pradeep Kumar
Singh, Prashant Kumar
Shankar, Hari
Yadav, Virendra S.
Katoch, Vishwa M.
Bajaj, Bharat
Gupta, Rajesh
Sengupta, Utpal
Joshi, Beenu
Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title_full Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title_fullStr Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title_full_unstemmed Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title_short Serodiagnostic Efficacy of Mycobacterium tuberculosis 30/32-kDa Mycolyl Transferase Complex, ESAT-6, and CFP-10 in Patients with Active Tuberculosis
title_sort serodiagnostic efficacy of mycobacterium tuberculosis 30/32-kda mycolyl transferase complex, esat-6, and cfp-10 in patients with active tuberculosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816261/
https://www.ncbi.nlm.nih.gov/pubmed/20049651
http://dx.doi.org/10.1007/s00005-009-0055-4
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