{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T09:07:13Z","timestamp":1762506433261,"version":"3.40.4"},"reference-count":22,"publisher":"S. Karger AG","issue":"3","license":[{"start":{"date-parts":[[2014,1,1]],"date-time":"2014-01-01T00:00:00Z","timestamp":1388534400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2014,1,1]],"date-time":"2014-01-01T00:00:00Z","timestamp":1388534400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Respiration"],"published-print":{"date-parts":[[2014]]},"abstract":"<jats:p>&lt;b&gt;&lt;i&gt;Background:&lt;\/i&gt;&lt;\/b&gt; Diagnosis and treatment monitoring of patients with tuberculosis remain challenging. &lt;b&gt;&lt;i&gt;Objective:&lt;\/i&gt;&lt;\/b&gt; We have evaluated whether &lt;i&gt;Mycobacterium&lt;\/i&gt;-specific interferon (IFN)-&amp;#947; and interleukin (IL)-2 bifunctional cytokine immune response assays improve the diagnosis of and correlate to treatment response in pulmonary tuberculosis. &lt;b&gt;&lt;i&gt;Methods:&lt;\/i&gt;&lt;\/b&gt; Early secretory antigenic target (ESAT)6\/culture filtrate protein 10 (CFP10), microsomal triglyceride transfer protein 65 (MTP65) and the purified protein derivative (PPD) tuberculin-specific immune profiles were investigated in peripheral blood mononuclear cells from 19 patients with culture-confirmed tuberculosis and 23 healthy community controls (HCCs; 82.6% with latent &lt;i&gt;M. tuberculosis&lt;\/i&gt; infection) using a novel fluorescence-based dual-colour enzyme-linked immunospot (EliSpot) technology (FluoroSpot). &lt;b&gt;&lt;i&gt;Results:&lt;\/i&gt;&lt;\/b&gt; The frequency of ESAT6\/CFP10-induced IFN-&amp;#947;+IL-2- producing cells was elevated (p &lt; 0.001), whereas the percentages of specific IFN-&amp;#947;-IL-2+ (p = 0.002) and IFN-&amp;#947;+IL-2+ double producing cells (p = 0.037) were diminished in tuberculosis patients in comparison to HCCs. A 3-host marker model using a combination of those IFN-&amp;#947; and IL-2 single-cell responses showed 93.8% sensitivity and 77.8% specificity for tuberculosis. During tuberculosis treatment, the PPD-induced immune responses shifted from an IFN-&amp;#947;+IL-2- dominated profile towards a balance of IFN-&amp;#947;-IL-2+ and IFN-&amp;#947;+IL-2+ double producing cells (all p \u2264 0.05). &lt;b&gt;&lt;i&gt;Conclusions:&lt;\/i&gt;&lt;\/b&gt; The addition of antigen-specific IL-2 production to IFN-&amp;#947; responses by EliSpot in IFN-&amp;#947; release assays increases diagnostic sensitivity for active tuberculosis.<\/jats:p>","DOI":"10.1159\/000365816","type":"journal-article","created":{"date-parts":[[2014,9,9]],"date-time":"2014-09-09T07:51:41Z","timestamp":1410249101000},"page":"251-261","source":"Crossref","is-referenced-by-count":16,"title":["Bifunctional T-Cell-Derived Cytokines for the Diagnosis of Tuberculosis and Treatment Monitoring"],"prefix":"10.1159","volume":"88","author":[{"given":"Paulin 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