Evidence map›Paper›PMID 41943056›Full record

ArticleBMC veterinary research2026

A monoclonal antibody-based, time-resolved fluorescence microsphere immunochromatographic testing strip for rapid and sensitive detection of H7 avian influenza viruses.

Han Wu, Ping Wang, Jiamin Fu, Fan Yang, Jing Guo, Linfang Cheng, Fumin Liu, Linwei Zhu, Hangping Yao, Nanping Wu and 2 more

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Han WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Ping WangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Jiamin FuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Fan YangDepartment of Geriatrics, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, 310009, China.
Jing GuoState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Linfang ChengState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Fumin LiuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Linwei ZhuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Hangping YaoState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Nanping WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China.
Lihua XuAnimal Husbandry and Veterinary Institute, Zhejiang Academy of Agricultural Science, Hangzhou, China.
Haibo WuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, and National Clinical Research Center for Infectious Diseases, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, Zhejiang, 310003, China. wuhaibo@zju.edu.cn.

Funding

National Science Foundation of China 32273092the Fundamental Research Funds for the Central Universities 2022ZFJH003the National Key R&D Program of China 2024YFC2309903Zhejiang Provincial Natural Science Foundation of China LQ23H190003Zhejiang Provincial Natural Science Foundation of China LY24H190001Zhejiang Provincial Natural Science Foundation of China QN25H190012
6 · The paper itself

Abstract

backgroundAvian influenza viruses (AIVs), particularly the H7N9 subtype, pose a persistent threat to global health security, having caused 1,687 human infections and 615 deaths to date. The significant socioeconomic impact and pandemic potential of H7N9 underscore the urgent need for rapid, reliable diagnostic tools to facilitate early intervention and control measures.

methodsThis study conducted on 2025 developed and optimized a time-resolved fluorescence microsphere immunochromatographic strip (TRFICS) assay for the rapid detection of H7 AIVs. The assay was constructed using two specific monoclonal antibodies, 2H9 and 1H9. Comprehensive evaluations were conducted to assess the assay’s sensitivity, specificity, reproducibility, and stability. Furthermore, clinical utility was validated by comparing TRFICS results with reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) using field samples (collected from 2013 to 2025).

resultsThe optimized TRFICS assay achieved limits of detection (LOD) of 2–5 hemagglutination units (HAU) for H7N9 in allantoic fluid and 0.01 ng/mL for purified H7N9 hemagglutinin protein within 15 min. The assay demonstrated 100% concordance with RT-qPCR results in field sample testing. High specificity was observed with no cross-reactivity against other prevalent pathogens. Additionally, the assay exhibited excellent repeatability (relative standard deviation < 8%) and maintained stable performance under various storage conditions.

conclusionThe developed TRFICS assay represents a robust, sensitive, and rapid platform for the on-site identification of H7 AIVs. Its superior performance characteristics make it a valuable tool for effective surveillance and timely response to potential H7 AIV pandemics.

Indexed as

Antibodies, MonoclonalChromatography, AffinityInfluenza A Virus, H7N9 SubtypeInfluenza in BirdsAnimalsLimit of DetectionMicrospheresRapid Diagnostic TestsReagent StripsReproducibility of ResultsSensitivity and SpecificityAntibodies, MonoclonalReagent StripsAvian influenza virusH7Immunochromatographic assayMonoclonal antibodiesTime-resolved fluorescence microsphere

Identifiers

PMID41943056
PMCPMC13188404

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LicenceCC BY-NC-ND
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Registered trials

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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.