Your browser doesn't support javascript.
loading
New synthetic lipid antigens for rapid serological diagnosis of tuberculosis.
Jones, Alison; Pitts, Mark; Al Dulayymi, Juma'a R; Gibbons, James; Ramsay, Andrew; Goletti, Delia; Gwenin, Christopher D; Baird, Mark S.
Afiliación
  • Jones A; School of Chemistry, Bangor University, Bangor, Gwynedd, Wales, United Kingdom.
  • Pitts M; School of Chemistry, Bangor University, Bangor, Gwynedd, Wales, United Kingdom.
  • Al Dulayymi JR; School of Chemistry, Bangor University, Bangor, Gwynedd, Wales, United Kingdom.
  • Gibbons J; School of Environment, Natural Resources and Geography, Bangor University, Bangor, Gwynedd, Wales, United Kingdom.
  • Ramsay A; Special Programme for Research and Training in Tropical Diseases (TDR), World Health Organisation, Geneva, Switzerland.
  • Goletti D; University of St Andrews Medical School, St. Andrews, Scotland, United Kingdom.
  • Gwenin CD; Translational Research Unit, Department of Epidemiology and Preclinical Research, 'L. Spallanzani' National Institute for Infectious Diseases, Rome, Italy.
  • Baird MS; School of Chemistry, Bangor University, Bangor, Gwynedd, Wales, United Kingdom.
PLoS One ; 12(8): e0181414, 2017.
Article en En | MEDLINE | ID: mdl-28806423
BACKGROUND: During pulmonary tuberculosis (PTB) antibodies are generated to trehalose esters of mycolic acids which are cell wall lipids of Mycobacterium tuberculosis (Mtb). Attempts have been made to use these complex natural mixtures in serological tests for PTB diagnosis. AIM: The aim of this work was to determine whether a serological test based on a panel of defined individual trehalose esters of characteristic synthetic mycolic acids has improved diagnostic accuracy in distinguishing patients with culture positive PTB from individuals who were Mtb culture negative. METHOD: One hundred serum samples from well-characterized patients with presumptive tuberculosis, and diagnosed as having pulmonary smear and culture positive TB, or being culture and smear negative were evaluated by ELISA using different combinations of synthetic antigens and secondary antibodies. Using cut-off values determined from these samples, we validated this study blind in samples from a further 249 presumptive TB patients. RESULTS: With the first 100 samples, detailed responses depended both on the precise structure of the antigen and on the secondary antibody. Using a single antigen, a sensitivity/specificity combination for smear and culture positive PTB detection of 85 and 88% respectively was achieved; this increased to 96% and 95% respectively by a statistical combination of the results with seven antigens. In the blind study a sensitivity/specificity of 87% and 83% was reached with a single antigen. With some synthetic antigens, the responses from all 349 samples were significantly better than those with the natural mixture. Combining the results for seven antigens allowed a distinction between culture positive and negative with a ROC AUC of 0.95. CONCLUSION: We have identified promising antigen candidates for serological assays that could be used to diagnose PTB and which could be the basis of a much-needed, simple, rapid diagnostic test that would bring care closer to communities.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tuberculosis Pulmonar / Pruebas Serológicas / Antígenos Bacterianos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tuberculosis Pulmonar / Pruebas Serológicas / Antígenos Bacterianos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido