Evidence map›Paper›PMID 41953018›Full record

ArticleFrontiers in immunology2026

Development and application of a VNAR-based detection nanobody for avian influenza virus H9N2.

Hongzhou Ye, Qingqing Dong, Min Qian, Yanwen Guo, Yi Chen, Wenyuan Liu, Lili Liu, Zhengbing Lyu, Chen Yuan, Xiaofeng Jiang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

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

10 authors.

Hongzhou Ye *Department of Pediatrics, The First Affiliated Hospital of Huzhou University, Huzhou, China.
Qingqing Dong *College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.
Min Qian *College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.
Yanwen Guo *College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.
Yi ChenDepartment of Pediatrics, The First Affiliated Hospital of Huzhou University, Huzhou, China.
Wenyuan LiuDepartment of Pediatrics, The First Affiliated Hospital of Huzhou University, Huzhou, China.
Lili LiuCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.
Zhengbing LyuCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.
Chen YuanDepartment of Pediatrics, The First Affiliated Hospital of Huzhou University, Huzhou, China.
Xiaofeng JiangCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Zhejiang Provincial Key Laboratory of Silkworm Bioreactor and Biomedicine, Zhejiang Sci-Tech University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The H9N2 subtype avian influenza virus, as a mutant strain of low-pathogenic avian influenza (LPAI), has augmented its transmission ability and pathogenicity via genetic evolution. At present, it has incurred the most substantial economic losses to the global poultry industry, particularly in Asia where it is extensively prevalent. To tackle this challenge, it is essential to devise effective prevention and control strategies for the H9N2 subtype. Among these strategies, vaccine development and highly sensitive diagnostic techniques are the primary countermeasures. Although more than twenty different vaccines and diagnostic kits for various types of avian influenza are currently available on the market, existing detection methods lack sufficient specificity for avian influenza virus subtypes. Precise subtype differentiation still depends on polymerase chain reaction (PCR)-based methods, which necessitate specialized equipment and are rarely accessible in on-site settings such as poultry farms. Our laboratory has developed specific single-domain antibodies (VNAR) derived from sharks against the H9N2 subtype of the avian influenza virus. The recombinant anti-H9N2 VNAR demonstrates high specificity for hemagglutinin (HA) binding activity and can specifically recognize, bind to, and neutralize the H9N2 subtype avian influenza virus on the surface of Madin-Darby canine kidney (MDCK) cells. Owing to their low molecular weight, excellent stability, and enhanced tissue penetration, these specific VNAR molecules possess extremely high application potential, rendering them innovative candidate drugs for the diagnosis and prevention of H9N2 infections.

Indexed as

Antibodies, ViralInfluenza A Virus, H9N2 SubtypeInfluenza in BirdsAnimalsAntibodies, NeutralizingDogsHemagglutinin Glycoproteins, Influenza VirusHumansMadin Darby Canine Kidney CellsAntibodies, NeutralizingAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusChiloscyllium plagiosumH9N2 subtype avian influenza virusMDCKprevention and treatmentVNAR

Identifiers

PMID41953018
PMCPMC13053647

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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.