QuantiFERON-TB supernatant-based biomarkers predicting active tuberculosis progression

IF 4.8 2区 医学 Q1 INFECTIOUS DISEASES
Haoxin Xu , Jingyu Zhou , Qingluan Yang , Yixuan Yang , Feiran Zhou , Mengqing Qian , Xing Lin , Wenhong Zhang , Lingyun Shao , Qiaoling Ruan
{"title":"QuantiFERON-TB supernatant-based biomarkers predicting active tuberculosis progression","authors":"Haoxin Xu ,&nbsp;Jingyu Zhou ,&nbsp;Qingluan Yang ,&nbsp;Yixuan Yang ,&nbsp;Feiran Zhou ,&nbsp;Mengqing Qian ,&nbsp;Xing Lin ,&nbsp;Wenhong Zhang ,&nbsp;Lingyun Shao ,&nbsp;Qiaoling Ruan","doi":"10.1016/j.ijid.2025.107915","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Despite the higher specificity and reliability of detecting latent tuberculosis (TB) infection, <em>Mycobacterium tuberculosis</em>-specific interferon (IFN)-γ release assays do not perform satisfactorily in predicting the risk of active TB (ATB) development. It is crucial to identify new biomarkers with high predictive accuracy to identify individuals bearing a high risk of progression.</div></div><div><h3>Methods</h3><div>This was a sub-study of an open-label, randomized clinical trial for prevention of TB in silicosis patients. Twenty-six participants were diagnosed with ATB within 37-month’ follow-up. They were defined as TB progressors and matched in a 1:2 ratio with 52 TB nonprogressors.</div></div><div><h3>Results</h3><div>We analyzed expression of 45 cytokines in QuantiFERON supernatants from TB progressors and nonprogressors, and granulocyte–macrophage colony-stimulating factor, vascular endothelial growth factor, interleukin (IL)-3, IFN-γ-induced protein 10, IL-10, and IL-9 outperformed IFN-γ as predictive markers.</div></div><div><h3>Conclusion</h3><div>These findings highlight the potential of new biomarkers in identifying individuals with high risk of TB to undergo early intervention.</div><div>Trial registration: ClinicalTrials.gov number: NCT02430259.</div></div>","PeriodicalId":14006,"journal":{"name":"International Journal of Infectious Diseases","volume":"157 ","pages":"Article 107915"},"PeriodicalIF":4.8000,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1201971225001389","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Despite the higher specificity and reliability of detecting latent tuberculosis (TB) infection, Mycobacterium tuberculosis-specific interferon (IFN)-γ release assays do not perform satisfactorily in predicting the risk of active TB (ATB) development. It is crucial to identify new biomarkers with high predictive accuracy to identify individuals bearing a high risk of progression.

Methods

This was a sub-study of an open-label, randomized clinical trial for prevention of TB in silicosis patients. Twenty-six participants were diagnosed with ATB within 37-month’ follow-up. They were defined as TB progressors and matched in a 1:2 ratio with 52 TB nonprogressors.

Results

We analyzed expression of 45 cytokines in QuantiFERON supernatants from TB progressors and nonprogressors, and granulocyte–macrophage colony-stimulating factor, vascular endothelial growth factor, interleukin (IL)-3, IFN-γ-induced protein 10, IL-10, and IL-9 outperformed IFN-γ as predictive markers.

Conclusion

These findings highlight the potential of new biomarkers in identifying individuals with high risk of TB to undergo early intervention.
Trial registration: ClinicalTrials.gov number: NCT02430259.
基于QuantiFERON-TB上清液的生物标志物预测活动性结核病进展。
背景:尽管检测潜伏结核感染具有更高的特异性和可靠性,但结核分枝杆菌特异性干扰素(IFN)-γ释放试验在预测活动性结核发展风险方面的效果并不令人满意。识别具有高预测准确性的新生物标志物对于识别具有高风险进展的个体至关重要。方法:这是一项预防矽肺患者结核病的开放标签随机临床试验的子研究。26名参与者在37个月的随访中被诊断为活动性结核病。他们被定义为结核病进展者,并以1:2的比例与52名结核病非进展者匹配。结果:我们分析了结核进展者和非进展者的QuantiFERON上清液中45种细胞因子的表达,粒细胞-巨噬细胞集落刺激因子、血管内皮生长因子、白细胞介素(IL)-3、IFN-γ诱导蛋白10 (IP-10)、IL-10和IL-9作为预测指标优于IFN-γ。结论:这些发现强调了新的生物标志物在识别结核病高风险个体进行早期干预方面的潜力。试验注册:ClinicalTrials.gov号码:NCT02430259。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
18.90
自引率
2.40%
发文量
1020
审稿时长
30 days
期刊介绍: International Journal of Infectious Diseases (IJID) Publisher: International Society for Infectious Diseases Publication Frequency: Monthly Type: Peer-reviewed, Open Access Scope: Publishes original clinical and laboratory-based research. Reports clinical trials, reviews, and some case reports. Focuses on epidemiology, clinical diagnosis, treatment, and control of infectious diseases. Emphasizes diseases common in under-resourced countries.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信