ArticleJournal of nanobiotechnology2026
A novel nanosensor for in situ detection of EV-miR-107 enables noninvasive tuberculosis diagnosis and treatment monitoring.
Article in Journal of nanobiotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
Abstract
Tuberculosis (TB) remains a leading cause of infectious death globally, creating an urgent need for rapid and non-invasive diagnostics. Extracellular vesicles (EVs) have emerged as promising carriers of disease-specific microRNAs with biomarker potential. This study identifies EV-miR-107 as a candidate host-response biomarker for TB, showing significant upregulation in TB patient plasma and a murine BCG infection model. To utilize this finding, an in-situ detection platform named CLiAN (CHA@Lipo@Aptamer Nanosensor) is developed. It utilizes cationic liposomes functionalized with CD63-specific aptamers and encapsulating catalytic hairpin assembly (CHA) probes to enable targeted EV fusion, facilitating efficient EV miRNA profiling within two hours. Clinically, CLiAN detects EV-miR-107 with 95.2% sensitivity (AUC = 0.87), outperforming sputum culture (36.4%) and Xpert MTB/RIF (54.5%). It also reliably monitors treatment response via dynamic changes in plasma EV-miR-107 levels (p = 0.001), correlating with clinical outcomes. This work establishes an integrated framework for TB management-from biomarker discovery to diagnostics and treatment monitoring-paving the way for improved point-of-care TB control.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.