首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Long-Incubation-Time Gamma Interferon Release Assays in Response to Purified Protein Derivative ESAT-6 and/or CFP-10 for the Diagnosis of Mycobacterium tuberculosis Infection in Children
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Long-Incubation-Time Gamma Interferon Release Assays in Response to Purified Protein Derivative ESAT-6 and/or CFP-10 for the Diagnosis of Mycobacterium tuberculosis Infection in Children

机译:纯化蛋白衍生物ESAT-6和/或CFP-10对儿童结核分枝杆菌感染诊断的长时间潜伏期γ干扰素释放分析

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摘要

The diagnosis of childhood active tuberculosis (aTB) and latent Mycobacterium tuberculosis (M. tuberculosis) infection (LTBI) remains a challenge, and the replacement of tuberculin skin tests (TST) with commercialized gamma interferon (IFN-γ) release assays (IGRA) is not currently recommended. Two hundred sixty-six children between 1 month and 15 years of age, 214 of whom were at risk of recent M. tuberculosis infection and 51 who were included as controls, were prospectively enrolled in our study. According to the results of a clinical evaluation, TST, chest X ray, and microbiological assessment, each children was classified as noninfected, having LTBI, or having aTB. Long-incubation-time purified protein derivative (PPD), ESAT-6, and CFP-10 IGRA were performed and evaluated for their accuracy in correctly classifying the children. Whereas both TST and PPD IGRA were suboptimal for detecting aTB, combining the CFP-10 IGRA with a TST or with a PPD IGRA allowed us to detect all the children with aTB with a specificity of 96% for children who were positive for the CFP-10 IGRA. Moreover, the combination of the CFP-10 IGRA and PPD IGRA detected 96% of children who were eventually classified as having LTBI, but a strong IFN-γ response to CFP-10 (defined as >500 pg/ml) was highly suggestive of aTB, at least among the children who were <3 years old. The use of long-incubation-time CFP-10 IGRA and PPD IGRA should help clinicians to quickly identify aTB or LTBI in young children.
机译:儿童活动性肺结核(aTB)和潜伏结核分枝杆菌(LTBI)感染的诊断仍然是一项挑战,用商业化的γ干扰素(IFN-γ)释放测定法(IGRA)替代结核菌素皮肤试验(TST)目前不推荐。前瞻性纳入了本研究的166名1个月至15岁之间的儿童,其中214名有近期发生结核分枝杆菌感染的危险,而51名作为对照被纳入研究。根据临床评估,TST,胸部X线和微生物学评估的结果,将每位儿童归为未感染,患有LTBI或患有aTB。进行了长时间孵育的纯化蛋白衍生物(PPD),ESAT-6和CFP-10 IGRA,并评估了它们对儿童正确分类的准确性。尽管TST和PPD IGRA都不是检测aTB的最佳方法,但将CFP-10 IGRA与TST或PPD IGRA结合使用可以使我们检测到所有ATB儿童,其CFP阳性儿童的特异性为96%。 10 IGRA。此外,CFP-10 IGRA和PPD IGRA的组合检测出96%的儿童最终被归类为LTBI,但是对CFP-10的强烈IFN-γ反应(定义为> 500 pg / ml)强烈提示aTB,至少在3岁以下的儿童中。长时间孵育的CFP-10 IGRA和PPD IGRA的使用应有助于临床医生快速识别幼儿中的aTB或LTBI。

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