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Interferon-Gamma Release Assays versus Tuberculin Skin Testing for the Diagnosis of Latent Tuberculosis Infection: An Overview of the Evidence

机译:干扰素-γ释放试验与结核菌素皮肤试验对潜伏性结核感染的诊断:证据概述

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摘要

A profusion of articles have been published on the accuracy and uses of interferon-gamma releasing assays. Here we review the clinical applications, advantages, and limitations of the tuberculin skin test and interferon-gamma release assays and provide an overview of the most recent systematic reviews conducted for different indications for the use of these tests. We conclude that both tests are accurate to detect latent tuberculosis, although interferon-gamma release assays have higher specificity than tuberculin skin testing in BCG-vaccinated populations, particularly if BCG is received after infancy. However, both tests perform poorly to predict risk for progression to active tuberculosis. Interferon-gamma release assays have significant limitations in serial testing because of spontaneous variability and lack of a validated definition of conversion and reversion, making it difficult for clinicians to interpret changes in category (conversions and reversions). So far, the most important clinical evidence, that is, that isoniazid preventive therapy reduces the risk for progression to disease, has been produced only in tuberculin skin test-positive individuals.
机译:关于干扰素-γ释放测定法的准确性和用途的大量文章已经发表。在这里,我们回顾了结核菌素皮肤试验和干扰素-γ释放试验的临床应用,优点和局限性,并概述了针对使用这些试验的不同适应症进行的最新系统评价。我们得出的结论是,尽管在接种了BCG的人群中,γ-干扰素释放试验的特异性比结核菌素皮肤试验高,但两种方法都可以准确检测潜伏性结核病,特别是如果婴儿期后接种BCG的话。但是,两项测试的表现均不佳,无法预测发展为活动性肺结核的风险。干扰素-γ释放测定法具有自发变异性,并且缺乏经过验证的转化和逆转定义,因此在串行测试中存在明显的局限性,这使得临床医生难以解释类别变化(转化和逆转)。迄今为止,最重要的临床证据,即异烟肼预防性治疗降低了疾病进展的风险,仅在结核菌素皮肤试验阳性的个体中产生。

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