潜伏性肺结核
医学
肺结核
人口
精密医学
生物标志物
免疫学
重症监护医学
临床实习
结核菌素
结核病诊断
测试策略
敏化
风险分析(工程)
考试(生物学)
相关性(法律)
作者
Ruizi Ni,Yanhua Liu,Alice Armanni,Giulia Ghisleni,Sara Fumagalli,Yajing An,Yiming Li,Li Zhuang,Yang Ling,Linsheng Li,Zhaoyang Ye,Antonia Daniele Souza Bruno,Lingxia Zhang,Wenping Gong
摘要
CD27⁻ T cells, and Fc-glycosylated antibodies) with pathogen-derived antigens (dormancy survival regulator [DosR], resuscitation-promoting factor [Rpf], heparin-binding hemagglutinin [HBHA], and PE/PPE) to create a three-tier index: single-analyte triage, multi-analyte confirmation, and dynamic treatment monitoring. At the technology level, we benchmark multi-omics-plus-AI models, single-molecule Simoa arrays, and microfluidic point-of-care testing (POCT) platforms for sensitivity, accessibility, and cost. High-quality cross-population validation, standardized thresholds, and resource-tiered deployment remain the principal translational bottlenecks. We call for integrated programs that combine key-population multicenter cohorts, explainable AI, and ASSURED criteria to propel LTBI management from the T-cell-sensitization era into the molecular-intelligent age. Achieving this vision within 5 years is technically feasible and will accelerate global elimination targets by enabling precision preventive therapy at an unprecedented scale.
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