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巴基斯坦儿童中用于诊断结核分枝杆菌感染的分泌抗体细胞。

Antibody-Secreting Cells To Diagnose Mycobacterium tuberculosis Infection in Children in Pakistan.

机构信息

Department of Paediatrics, Aga Khan University, Karachi, Pakistan

Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.

出版信息

mSphere. 2020 Feb 5;5(1):e00632-19. doi: 10.1128/mSphere.00632-19.

DOI:10.1128/mSphere.00632-19
PMID:32024709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7002306/
Abstract

Reliance on microbiologic methods to diagnose infection is a suboptimal approach for children due in part to the paucibacillary nature of the disease. A blood-based biomarker assay, such as the mycobacterial-antibody-secreting cell (MASC) assay, could be a major advance for the field of study of pediatric tuberculosis (TB). Children <15 years of age with clinical concern for TB and age-matched children with no concern for TB were enrolled from outpatient clinics in Karachi, Pakistan. MASC, ferritin, and C-reactive protein (CRP) assays were performed, and results were compared among cases and controls, as well as among children with a case definition of "confirmed TB," "probable TB," or "possible TB." MASC responses were significantly higher among children with TB than among controls (0.41 optical density [OD] versus 0.28 OD, respectively,  < 0.001), and the differences were largely driven by the data from children with confirmed TB ( = 0.002). Ferritin and CRP values were significantly higher among those with confirmed TB than among those with the other disease states and controls ( = 0.004 and  = 0.019, respectively). The use of the MASC assay as a blood-based biomarker for TB disease shows some promise among children with microbiologically confirmed disease; however, the performance characteristics for the majority of young children with unconfirmed TB were suboptimal in this cohort. Tuberculosis (TB) in children represents a missed opportunity for diagnosis and preventive therapy. The magnitude or burden of disease in children is not fully understood due to our limitations with respect to exploring sensitive diagnostic algorithms. In a setting of TB endemicity in Pakistan, we carried out a proof-of-concept study to evaluate for the first time the performance of B cell analyses by the use of well-defined diagnostic criteria and NIH consensus guidelines as "culture-confirmed," "probable," and "possible" TB groups. In contrast to detection of serum antibody, we focused on mycobacterial-antibody-secreting cell (MASC) detection as a marker of active disease in children with a strong suspicion of TB. Further work exploring a larger panel of inflammatory biomarkers and enrichment of B cells with the objective of increasing the sensitivity of the current MASC assay would lead to the development of a field-friendly assay for timely diagnosis of childhood TB.

摘要

由于疾病的菌量少,依靠微生物方法来诊断感染对儿童来说并不是一种最佳方法。一种基于血液的生物标志物检测方法,如分枝杆菌抗体分泌细胞(MASC)检测,可能是研究儿童结核病(TB)领域的重大进展。从巴基斯坦卡拉奇的门诊诊所招募了 15 岁以下有结核病临床疑虑的儿童和年龄匹配的无结核病疑虑的儿童。进行了 MASC、铁蛋白和 C 反应蛋白(CRP)检测,并比较了病例和对照组以及具有“确诊结核病”、“可能结核病”或“可能结核病”病例定义的儿童之间的结果。与对照组相比,结核病患儿的 MASC 反应明显更高(分别为 0.41 光密度(OD)和 0.28 OD,  < 0.001),差异主要来自确诊结核病患儿的数据( = 0.002)。与其他疾病状态和对照组相比,确诊结核病患儿的铁蛋白和 CRP 值明显更高( = 0.004 和  = 0.019)。MASC 检测作为一种基于血液的结核病生物标志物,在有微生物学确诊疾病的儿童中显示出一定的前景;然而,在本队列中,大多数未确诊结核病的年幼儿童的表现特征并不理想。儿童结核病是诊断和预防治疗的一个错失的机会。由于我们在探索敏感诊断算法方面的局限性,儿童疾病的严重程度或负担尚不完全清楚。在巴基斯坦结核病流行的背景下,我们进行了一项概念验证研究,首次使用明确的诊断标准和 NIH 共识指南作为“培养确诊”、“可能”和“可能”结核病组,评估 B 细胞分析的性能。与检测血清抗体不同,我们专注于分枝杆菌抗体分泌细胞(MASC)检测,作为怀疑结核病的儿童活动性疾病的标志物。进一步探索更大的炎症生物标志物面板并富集 B 细胞,以提高当前 MASC 检测的灵敏度,将有助于开发一种便于现场使用的检测方法,以便及时诊断儿童结核病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/a58b523b6e53/mSphere.00632-19-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/506ecab4acb0/mSphere.00632-19-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/a58b523b6e53/mSphere.00632-19-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/506ecab4acb0/mSphere.00632-19-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/9aa4fa434e1d/mSphere.00632-19-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/969315e8dc71/mSphere.00632-19-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924f/7002306/18456de1b11c/mSphere.00632-19-f0004.jpg
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