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全血样本中降钙素原、C反应蛋白和α-1酸性糖蛋白水平升高有助于快速鉴别活动性肺结核与潜伏性结核感染及健康个体。

High Procalcitonin, C-Reactive Protein, and α-1 Acid Glycoprotein Levels in Whole Blood Samples Could Help Rapid Discrimination of Active Tuberculosis from Latent Tuberculosis Infection and Healthy Individuals.

作者信息

Kang Yun-Jeong, Park Heechul, Park Sung-Bae, Lee Jiyoung, Hyun Hyanglan, Jung Minju, Lee Eun Ju, Je Min-A, Kim Jungho, Lee Yong Sung, Kim Sunghyun

机构信息

Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.

Department of Laboratory Medicine, Good Samsun Hospital, Busan 47007, Korea.

出版信息

Microorganisms. 2022 Sep 28;10(10):1928. doi: 10.3390/microorganisms10101928.

Abstract

Tuberculosis (TB) management is important for prompt discrimination of latent TB infection (LTBI) from active TB and proper treatment. Whole blood Interferon-gamma (IFN-γ) release assay (IGRA) is used to diagnose LTBI based on the secretion of IFN-γ by T-cells in the whole blood by using a specific antigen of Mycobacterium tuberculosis. However, the ability of IGRA to distinguish active TB from LTBI is considerably limited. Distinguishing active TB from LTBI is necessary to identify indicators that can be used to effectively manage TB and develop diagnostic methods. In the present study, we used a Luminex multiplex bead array (a bead-based antibody−antigen sandwich method). The whole blood level of acute phase proteins (APPs), such as endoglin (ENG), procalcitonin (PCT), C-reactive protein (CRP), and α1-acid glycoprotein (AGP), in active TB, LTBI, and healthy individuals were analyzed and quantified. The APP test results for the serum and whole blood samples showed that the levels of PCT, CRP, and AGP were significantly increased (p < 0.0500; area under curve = 0.955) in active TB. The level of these markers in the whole blood of active TB, LTBI, and healthy individuals could provide data for effective diagnosis and treatment of TB.

摘要

结核病(TB)管理对于迅速区分潜伏性结核感染(LTBI)和活动性结核以及进行恰当治疗至关重要。全血干扰素-γ(IFN-γ)释放试验(IGRA)用于诊断LTBI,其原理是利用结核分枝杆菌的特异性抗原刺激全血中的T细胞分泌IFN-γ。然而,IGRA区分活动性结核和LTBI的能力相当有限。区分活动性结核和LTBI对于确定可用于有效管理结核病的指标以及开发诊断方法很有必要。在本研究中,我们使用了Luminex多重微珠阵列(一种基于微珠的抗体-抗原夹心方法)。分析并定量了活动性结核、LTBI患者及健康个体全血中急性期蛋白(APPs)的水平,如内皮糖蛋白(ENG)、降钙素原(PCT)、C反应蛋白(CRP)和α1-酸性糖蛋白(AGP)。血清和全血样本的APP检测结果显示,活动性结核患者的PCT、CRP和AGP水平显著升高(p < 0.0500;曲线下面积 = 0.955)。活动性结核、LTBI患者及健康个体全血中这些标志物的水平可为结核病的有效诊断和治疗提供数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebf9/9611162/dbfe30358aa9/microorganisms-10-01928-g001.jpg

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