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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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SP Birkhäuser Verlag Basel
2010
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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. |
format | Text |
id | pubmed-2816261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | SP Birkhäuser Verlag Basel |
record_format | MEDLINE/PubMed |
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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