Papworth Hospital NHs Foundation Trust, Papworth Everard, Cambridge CB23 3RE, UK.
Expert Rev Respir Med. 2014 Feb;8(1):67-78. doi: 10.1586/17476348.2014.852471. Epub 2013 Dec 2.
Interferon-gamma release assays (IGRAs) represent the first new tool to diagnose latent tuberculosis infection for more than 100 years. They have advantages over the traditional tuberculin skin test which has a poor specificity due to false-positive responses in people who are BCG vaccinated as there is a cross-reactivity of proteins present in both BCG and the tuberculin skin test. IGRAs rely on the concept of detecting the ex vivo release of the cytokine IFN-γ, a key anti-Mycobacterium tuberculosis cytokine, from T cells which react specifically to antigens from M. tuberculosis. T cells are sensitized to the antigens in vivo, and then react when they encounter the same proteins ex vivo. The readouts are used to determine presence of sensitized cells, acting as a surrogate for latent tuberculosis infection. IGRAs are now being incorporated into national guidance for diagnosis and research is ongoing into next-generation versions of the test.
干扰素释放试验(IGRAs)代表了 100 多年来诊断潜伏性结核感染的第一个新工具。它们优于传统的结核菌素皮肤试验,因为结核菌素皮肤试验由于在接种卡介苗的人群中出现假阳性反应而特异性较差,因为在卡介苗和结核菌素皮肤试验中存在蛋白质的交叉反应。IGRAs 依赖于检测细胞因子 IFN-γ(一种关键的抗结核分枝杆菌细胞因子)在体外释放的概念,这种释放来自于对结核分枝杆菌抗原特异性反应的 T 细胞。T 细胞在体内对这些抗原产生敏感性,然后当它们在体外遇到相同的蛋白质时就会发生反应。检测结果用于确定致敏细胞的存在,作为潜伏性结核感染的替代指标。IGRAs 现正被纳入国家诊断指南,并且正在对下一代的测试版本进行研究。