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巴西结核病患者对结核分枝杆菌特异性抗原ESAT-6的T细胞反应。

T-cell responses to the Mycobacterium tuberculosis-specific antigen ESAT-6 in Brazilian tuberculosis patients.

作者信息

Cardoso Fernando L L, Antas Paulo R Z, Milagres Alexandre S, Geluk Annemieke, Franken Kees L M C, Oliveira Eliane B, Teixeira Henrique C, Nogueira Susie A, Sarno Euzenir N, Klatser Paul, Ottenhoff Tom H M, Sampaio Elizabeth P

机构信息

Leprosy Laboratory, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.

出版信息

Infect Immun. 2002 Dec;70(12):6707-14. doi: 10.1128/IAI.70.12.6707-6714.2002.

Abstract

The Mycobacterium tuberculosis-specific ESAT-6 antigen induces highly potent T-cell responses and production of gamma interferon (IFN-gamma), which play a critical role in protective cell-mediated immunity against tuberculosis (TB). In the present study, IFN-gamma secretion by peripheral blood mononuclear cells (PBMCs) in response to M. tuberculosis ESAT-6 in Brazilian TB patients was investigated in relation to clinical disease types, such as pleurisy and cavitary pulmonary TB. Leprosy patients, patients with pulmonary diseases other than TB, and healthy donors were assayed as control groups. Sixty percent of the TB patients indeed recognized M. tuberculosis ESAT-6, as did 50% of the leprosy patients and 60% of the non-TB controls. Nevertheless, the levels of IFN-gamma in response to the antigen ESAT, but not to antigen 85B (Ag85B) and purified protein derivative (PPD), were significantly lower in controls than in patients with treated TB or pleural or cavitary TB. Moreover, according to Mycobacterium bovis BCG vaccination status, only 59% of the vaccinated TB patients responded to ESAT in vitro, whereas 100% of them responded to PPD. Both CD4 and CD8 T cells were able to release IFN-gamma in response to ESAT. The present data demonstrate the specificity of ESAT-6 of M. tuberculosis and its ability to discriminate TB patients from controls, including leprosy patients. However, to obtain specificity, it is necessary to include quantitative IFN-gamma production in response to the antigen as well, and this might limit the use of ESAT-6-based immunodiagnosis of M. tuberculosis infection in an area of TB endemicity.

摘要

结核分枝杆菌特异性早期分泌性抗原靶6(ESAT-6)抗原可诱导高效的T细胞反应并产生γ干扰素(IFN-γ),这在针对结核病(TB)的保护性细胞介导免疫中起关键作用。在本研究中,针对巴西结核病患者外周血单个核细胞(PBMC)对结核分枝杆菌ESAT-6的反应所分泌的IFN-γ,与胸膜炎和空洞型肺结核等临床疾病类型进行了相关性研究。麻风病患者、非结核性肺部疾病患者和健康供体作为对照组进行检测。60%的结核病患者确实能识别结核分枝杆菌ESAT-6,50%的麻风病患者和60%的非结核对照组也能识别。然而,对照组中针对抗原ESAT(而非抗原85B(Ag85B)和纯化蛋白衍生物(PPD))产生的IFN-γ水平显著低于已治疗的结核病患者、胸膜炎或空洞型肺结核患者。此外,根据卡介苗(BCG)接种状态,仅59%接种过疫苗的结核病患者在体外对ESAT有反应,而他们对PPD的反应率为100%。CD4和CD8 T细胞均能对ESAT产生反应并释放IFN-γ。目前的数据证明了结核分枝杆菌ESAT-6的特异性及其区分结核病患者与包括麻风病患者在内的对照组的能力。然而,为了获得特异性,还需要包括针对该抗原产生的定量IFN-γ,而这可能会限制在结核病流行地区基于ESAT-6的结核分枝杆菌感染免疫诊断的应用。

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