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干扰素γ释放试验:原理与实践。

Interferon gamma release assays: principles and practice.

机构信息

Tuberculosis Research Unit, Department of Respiratory Medicine, National Heart and Lung Institute, Imperial College London, London, UK.

出版信息

Enferm Infecc Microbiol Clin. 2010 Apr;28(4):245-52. doi: 10.1016/j.eimc.2009.05.012. Epub 2009 Sep 24.

Abstract

The last decade has witnessed significant advances in mycobacterial genomics and cellular research which have resulted in the development of two new blood tests, the enzyme-linked immunospot assay (ELISpot) (TSPOT.TB, Oxford Immunotec, Oxford, UK) and the enzyme-linked immunosorbent assay (ELISA) (QuantiFERON-TB Gold In-Tube, Cellestis, Carnegie, Australia). These tests, which are collectively known as interferon gamma release assays (IGRAs), detect latent tuberculosis infection (LTBI) by measuring interferon (IFN)-gamma release in response to antigens present in Mycobacterium tuberculosis, but not bacille Calmette-Guerin (BCG) vaccine and most nontuberculous mycobacteria. This is done through enumeration of IFN-gamma-secreting T cells (ELISpot) or by measurement of IFN-gamma concentration (ELISA). The evidence base for these tests has expanded rapidly and now demonstrates that IGRAs are more specific than the tuberculin skin test (TST) as they are not confounded by previous BCG vaccination. In addition, with active tuberculosis (TB) as a surrogate for LTBI, it appears that the ELISA has a similar sensitivity to the TST, whereas the ELISpot is more sensitive. Using degree of exposure to TB as a surrogate for LTBI, both assays correlate at least as well with TB exposure as the TST. Recent longitudinal data have now demonstrated the prognostic power of positive IGRA results in recent contacts for the subsequent progression to active TB. Deployment of IGRAs, driven by new guidelines internationally, will impact on clinical practice in several ways. Their high specificity means that BCG-vaccinated individuals with a false-positive TST will not receive unnecessary preventive treatment, whereas improved sensitivity in individuals with weakened cellular immunity at highest risk of progressing to active TB (for example HIV-positive individuals) enables more reliable targeted testing and treatment of these vulnerable groups. The role of IGRAs in active TB is less clear but they may be useful as adjunctive tests in the diagnostic work-up of an individual with suspected TB. Finally, recent developments and future directions in IGRA development are reviewed.

摘要

过去十年见证了分枝杆菌基因组学和细胞研究的重大进展,这导致了两种新的血液检测方法的发展,酶联免疫斑点检测(ELISpot)(TSPOT.TB,牛津免疫技术公司,英国牛津)和酶联免疫吸附检测(ELISA)(QuantiFERON-TB Gold In-Tube,Cellestis,澳大利亚卡内基)。这些检测方法统称为干扰素γ释放分析(IGRA),通过测量对结核分枝杆菌存在的抗原的干扰素(IFN)-γ释放来检测潜伏性结核感染(LTBI),但不包括卡介苗(BCG)疫苗和大多数非结核分枝杆菌。这是通过计数 IFN-γ分泌 T 细胞(ELISpot)或测量 IFN-γ浓度(ELISA)来完成的。这些检测方法的证据基础迅速扩大,现在表明 IGRA 比结核菌素皮肤试验(TST)更具特异性,因为它们不受先前 BCG 疫苗接种的干扰。此外,由于活动性结核病(TB)是 LTBI 的替代指标,似乎 ELISA 与 TST 具有相似的敏感性,而 ELISpot 则更敏感。使用 TB 暴露程度作为 LTBI 的替代指标,两种检测方法与 TST 一样,与 TB 暴露至少具有同等相关性。最近的纵向数据现在证明了 IGRA 阳性结果在最近接触者中对随后发展为活动性 TB 的预后能力。国际新指南的推动下,IGRA 的应用将在几个方面影响临床实践。它们的高特异性意味着,BCG 疫苗接种者的 TST 假阳性不会接受不必要的预防性治疗,而在细胞免疫功能较弱的个体中,对进展为活动性 TB 的风险最高的个体中,敏感性的提高(例如 HIV 阳性个体)使得对这些弱势群体进行更可靠的靶向检测和治疗成为可能。IGRA 在活动性 TB 中的作用尚不明确,但它们可能是疑似 TB 患者诊断的辅助检测方法。最后,审查了 IGRA 开发的最新进展和未来方向。

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