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美国用于检测结核分枝杆菌感染的QuantiFERON-TB Gold检测指南

Guidelines for using the QuantiFERON-TB Gold test for detecting Mycobacterium tuberculosis infection, United States.

作者信息

Mazurek Gerald H, Jereb John, Lobue Phillip, Iademarco Michael F, Metchock Beverly, Vernon Andrew

出版信息

MMWR Recomm Rep. 2005 Dec 16;54(RR-15):49-55.

Abstract

On May 2, 2005, a new in vitro test, QuantiFERON-TB Gold (QFT-G, Cellestis Limited, Carnegie, Victoria, Australia), received final approval from the U.S. Food and Drug Administration as an aid for diagnosing Mycobacterium tuberculosis infection. This test detects the release of interferon-gamma (IFN-g) in fresh heparinized whole blood from sensitized persons when it is incubated with mixtures of synthetic peptides representing two proteins present in M. tuberculosis: early secretory antigenic target-6 (ESAT-6) and culture filtrate protein-10 (CFP-10). These antigens impart greater specificity than is possible with tests using purified protein derivative as the tuberculosis (TB) antigen. In direct comparisons, the sensitivity of QFT-G was statistically similar to that of the tuberculin skin test (TST) for detecting infection in persons with untreated culture-confirmed tuberculosis (TB). The performance of QFT-G in certain populations targeted by TB control programs in the United States for finding latent TB infection is under study. Its ability to predict who eventually will have TB disease has not been determined, and years of observational study of substantial populations would be needed to acquire this information. In July 2005, CDC convened a meeting of consultants and researchers with expertise in the field to review scientific evidence and clinical experience with QFT-G. On the basis of this review and discussion, CDC recommends that QFT-G may be used in all circumstances in which the TST is currently used, including contact investigations, evaluation of recent immigrants, and sequential-testing surveillance programs for infection control (e.g., those for health-care workers). This report provides specific cautions for interpreting negative QFT-G results in persons from selected populations. This report is aimed at public health officials, health-care providers, and laboratory workers with responsibility for TB control activities in the United States.

摘要

2005年5月2日,一项新的体外检测方法——结核菌素释放试验金标法(QFT-G,澳大利亚维多利亚州卡内基市Cellestis有限公司)获得了美国食品药品监督管理局的最终批准,可用于辅助诊断结核分枝杆菌感染。该检测方法通过将新鲜的肝素化全血与代表结核分枝杆菌中两种蛋白质的合成肽混合物孵育,来检测致敏者体内干扰素-γ(IFN-γ)的释放。这两种蛋白质分别是早期分泌性抗原靶标6(ESAT-6)和培养滤液蛋白10(CFP-10)。与使用纯化蛋白衍生物作为结核(TB)抗原的检测方法相比,这些抗原具有更高的特异性。在直接比较中,QFT-G在检测未经治疗且培养确诊为结核病(TB)患者的感染时,其敏感性在统计学上与结核菌素皮肤试验(TST)相似。QFT-G在美国结核病控制项目针对某些人群筛查潜伏性结核感染方面的性能正在研究中。其预测谁最终会患结核病的能力尚未确定,需要对大量人群进行多年的观察性研究才能获得此信息。2005年7月,美国疾病控制与预防中心(CDC)召集了该领域的顾问和研究人员会议,以审查QFT-G的科学证据和临床经验。基于此次审查和讨论,CDC建议在目前使用TST的所有情况下都可使用QFT-G,包括接触者调查、近期移民评估以及感染控制的序贯检测监测项目(例如针对医护人员的项目)。本报告针对特定人群中QFT-G阴性结果的解读提供了具体的注意事项。本报告面向美国负责结核病控制活动的公共卫生官员、医护人员和实验室工作人员。

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