ArticleBMC medicine2025
A point-of-care testing device for monkeypox virus integrating recombinase polymerase amplification and lateral flow assay.
Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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
1 citing paper in PubMed.
- A retrospective comparative diagnostic evaluation of three commercial qPCR kits for the diagnosis of mpox virus on an enriched sample set.Frontiers in cellular and infection microbiology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
backgroundThe global spread of monkeypox virus (MPXV) underscores the need for rapid, accessible diagnostic tools to control outbreaks. Current diagnostics, relying on centralized laboratory testing, require specialized personnel and equipment. We aimed to develop a point-of-care testing (POCT) kit that simplifies nucleic acid extraction, minimizes contamination, and enables immediate, accurate MPXV detection.
methodsWe introduced a novel MPXV POCT kit, featuring a separate MPXV DNA rapid release step and a closed integrated device combining recombinase polymerase amplification (RPA) and lateral flow assay (LFA). A fluorescent RPA assay identified F3L-targeting primers and probes with superior amplification efficiency. The RPA system was coupled with LFA to assess the visual diagnostic performance, and then integrated into a POCT device, complemented by a nucleic acid release agent to form the kit. The kit's specificity, sensitivity, and diagnostic performance were validated through clinical body fluid samples.
resultsOur nucleic acid release agent streamlines sample processing without compromising detection accuracy, eliminating the need for traditional nucleic acid extraction. The RPA reaction system was formulated into freeze-dried microspheres and integrated directly into the reaction chamber of the POCT device, ensuring the stability and shelf-life of the reagents and simplifying the preparation and configuration process. The POCT device's enclosed design eradicates transfer steps, significantly reducing RPA-induced aerosol contamination. Results can be visually interpreted within 25 min, a substantial improvement over existing methods. In clinical sample validation, the POCT kit showed high specificity and sensitivity, distinguishing other pathogens, with 100% consistency with RT-qPCR results in detecting mpox patient samples. Compared to RT-qPCR and ddPCR, our POCT kit demonstrates stronger diagnostic performance, with the lowest positive concentration we detected being 41 copies/mL (2.1 copies/reaction) in clinical samples and 2.5 copies/μL (2.5 copies/reaction) of DNA plasmid standards, significantly increasing the detection rate of mpox.
conclusionsThis compact, portable POCT kit, requiring no professional operation or precision instruments, offers a promising solution for on-site and home self-testing. Its high sensitivity and specificity, coupled with the capacity to swiftly adapt to new MPXV strains, positions it as an effective tool for early detection, vital for controlling mpox outbreaks.
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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.