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A TB antigen-stimulated CXCR3 ligand assay for the diagnosis of active pulmonary TB.
Chung, Wou Young; Lee, Keu Sung; Jung, Yun Jung; Lee, Hye Lim; Kim, Young Sun; Park, Joo Hun; Sheen, Seung Soo; Park, Kwang Joo.
Afiliación
  • Chung WY; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Lee KS; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Jung YJ; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Lee HL; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Kim YS; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Park JH; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Sheen SS; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea.
  • Park KJ; Department of Pulmonary and Critical Care Medicine, Ajou University School of Medicine, Suwon, South Korea. Electronic address: parkkj@ajou.ac.kr.
Chest ; 146(2): 283-291, 2014 Aug.
Article en En | MEDLINE | ID: mdl-24577604
BACKGROUND: The ligands for CXC chemokine receptor 3 (CXCR3) recruit T-helper type 1 cells, which play a major role in cell-mediated immunity in TB. METHODS: A total of 409 subjects were enrolled. The study population comprised 186 patients with active TB, 58 patients with non-TB pulmonary diseases, 50 control subjects with a positive interferon (IFN)-γ release assay (IGRA) result, and 115 control subjects with a negative IGRA result. Whole-blood samples were collected using IGRA methodology. After incubation, plasma IFN-γ levels and two CXCR3 ligands, IFN-inducible T-cell α-chemoattractant (I-TAC, CXCL11) and monokine induced by IFN-γ (MIG, CXCL9), were measured by enzyme-linked immunosorbent assay. Receiver operating characteristic (ROC) analysis was performed. Sensitivity and specificity were based on cutoff values selected to maximize the Youden index. RESULTS: The TB antigen-stimulated levels of IFN-γ, I-TAC, and MIG were significantly increased in the active pulmonary TB group compared with all other groups. From ROC analysis, for the diagnosis of active TB, I-TAC and MIG outperformed IFN-γ in all comparisons with the IGRA-positive and -negative control groups and the non-TB pulmonary disease group. The areas under the curve (95% CI) for differentiating active pulmonary TB from all other groups were 0.893 (0.864-0.924) for IFN-γ, 0.962 (0.946-0.978) for I-TAC, and 0.944 (0.922-0.965) for MIG. Sensitivity and specificity were 90.3% and 90.7%, respectively, for I-TAC; 92.5% and 85.2% for MIG; and 84.9% and 79.8% for IFN-γ. CONCLUSIONS: TB antigen-stimulated assays of I-TAC and MIG may be useful surrogate markers in the diagnosis of active pulmonary TB.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tuberculosis Pulmonar / Células TH1 / Receptores CXCR3 / Inmunidad Celular / Mycobacterium tuberculosis / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Chest Año: 2014 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tuberculosis Pulmonar / Células TH1 / Receptores CXCR3 / Inmunidad Celular / Mycobacterium tuberculosis / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Chest Año: 2014 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Estados Unidos