QuantiFERON Supernatant-Based Host Biomarkers Predicting Progression to Active Tuberculosis Disease Among Household Contacts of Tuberculosis Patients

医学 肺结核 量子化子 免疫学 降钙素原 接收机工作特性 多路复用 结核菌素 内科学 干扰素γ 结核分枝杆菌 置信区间 曲线下面积 优势比 潜伏性肺结核 细胞因子 病理 生物信息学 败血症 生物
作者
Evangeline Ann Daniel,Kannan Thiruvengadam,Anuradha Rajamanickam,Chandrasekaran Padmapriyadarsini,Sathyamurthi Pattabiraman,Brindha Bhanu,Amsaveni Sivaprakasam,Mandar Paradkar,Vandana Kulkarni,Rajesh Karyakarte,Shri Vijay Bala Yogendra Shivakumar,Vidya Mave,Amita Gupta,Subash Babu,Luke Elizabeth Hanna
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:76 (10): 1802-1813 被引量:6
标识
DOI:10.1093/cid/ciac979
摘要

Abstract Background The positive predictive value of tuberculin skin test and current generation interferon gamma release assays are very low leading to high numbers needed to treat. Therefore, it is critical to identify new biomarkers with high predictive accuracy to identify individuals bearing high risk of progression to active tuberculosis (TB). Methods We used stored QuantiFERON supernatants from 14 household contacts of index TB patients who developed incident active TB during a 2-year follow-up and 20 age and sex-matched non-progressors. The supernatants were tested for an expanded panel of 45 cytokines, chemokines, and growth factors using the Luminex Multiplex Array kit. Results We found significant differences in the levels of TB-antigen induced production of several analytes between progressors and non-progressors. Dominance analysis identified 15 key predictive biomarkers based on relative percentage importance. Principal component analysis revealed that these biomarkers could robustly distinguish between the 2 groups. Receiver operating characteristic analysis identified interferon-γ inducible protein (IP)-10, chemokine ligand (CCL)19, interferon (IFN)-γ, interleukin (IL)-1ra, CCL3, and granulocyte-macrophage colony-stimulating factor (GM-CSF) as the most promising predictive markers, with area under the curve (AUC) ≥90. IP-10/CCL19 ratio exhibited maximum sensitivity and specificity (100%) for predicting progression. Through Classification and Regression Tree analysis, a cutoff of 0.24 for IP-10/CCL19 ratio was found to be ideal for predicting short-term risk of progression to TB disease with a positive predictive value of 100 (95% confidence interval [CI] 85.8–100). Conclusions The biomarkers identified in this study will pave way for the development of a more accurate test that can identify individuals at high risk for immediate progression to TB disease for targeted intervention.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
大模型应助阁主采纳,获得10
刚刚
1秒前
2秒前
2秒前
popcorn完成签到,获得积分10
2秒前
2秒前
2秒前
twotwomi完成签到,获得积分10
2秒前
ly完成签到,获得积分20
3秒前
ChenYifei完成签到,获得积分10
3秒前
3秒前
4秒前
4秒前
Lucas应助来日方长采纳,获得10
4秒前
chang发布了新的文献求助10
4秒前
小巫发布了新的文献求助10
5秒前
周娅敏发布了新的文献求助10
6秒前
华仔应助答辩采纳,获得10
6秒前
caixiayin发布了新的文献求助10
6秒前
6秒前
威武的冷风关注了科研通微信公众号
7秒前
7秒前
7秒前
7秒前
8秒前
科研通AI2S应助奋斗若风采纳,获得10
8秒前
ly发布了新的文献求助10
8秒前
9秒前
xiang完成签到,获得积分10
9秒前
李爱国应助迷恋采纳,获得10
9秒前
在摆烂的dog完成签到,获得积分10
10秒前
星辰大海应助刘源采纳,获得10
10秒前
小巫完成签到,获得积分10
11秒前
ironsilica完成签到,获得积分10
11秒前
土豪的土豆完成签到 ,获得积分10
11秒前
orixero应助风趣的鸡翅采纳,获得10
12秒前
独步旋碟发布了新的文献求助10
12秒前
prime完成签到,获得积分10
12秒前
李木子完成签到 ,获得积分10
12秒前
高分求助中
A new approach to the extrapolation of accelerated life test data 1000
Handbook of Marine Craft Hydrodynamics and Motion Control, 2nd Edition 500
‘Unruly’ Children: Historical Fieldnotes and Learning Morality in a Taiwan Village (New Departures in Anthropology) 400
Indomethacinのヒトにおける経皮吸収 400
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 350
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3987223
求助须知:如何正确求助?哪些是违规求助? 3529513
关于积分的说明 11245651
捐赠科研通 3268108
什么是DOI,文献DOI怎么找? 1804027
邀请新用户注册赠送积分活动 881303
科研通“疑难数据库(出版商)”最低求助积分说明 808650