Evidence map›Paper›PMID 42237749›Full record

ArticleMicrobial biotechnology2026

Applying Baculovirus Surface Display Technology for Influenza Cytokine Profiling, Serological Detection and Antiviral Screening.

Li-Yun Cheng, Zheng Yu Phan, Chi-Wei Wang, Ching-Fen Shen, Ping-Chung Kuo, Hao-Ze Li, Yu-Chan Chao, Chih-Hsuan Tsai

Abstract read
In one paragraph

Article in Microbial biotechnology, 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
–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

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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

8 authors.

Li-Yun ChengDepartment of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.
Zheng Yu PhanDepartment of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.
Chi-Wei WangDepartment of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.
Ching-Fen ShenDepartment of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.
Ping-Chung KuoSchool of Pharmacy, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.ORCID https://orcid.org/0000-0003-3019-1138
Hao-Ze LiSchool of Pharmacy, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.ORCID https://orcid.org/0009-0008-4929-9898
Yu-Chan ChaoDepartment of Entomology, National Chung-Hsing University, College of Agriculture and Natural Resources, Taichung, Taiwan, ROC.
Chih-Hsuan TsaiDepartment of Microbiology and Immunology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.ORCID https://orcid.org/0000-0002-6395-0789

Funding

Chi Mei Medical Center CMNCKU11410National Cheng Kung University Hospital NCKUH-11210024National Cheng Kung University Hospital NCKUH-11302014National Cheng Kung University Hospital NCKUH-11502020National Science and Technology Council (Taiwan) NSTC 112-2320-B-006-056National Science and Technology Council (Taiwan) NSTC 113-2320-B-006-027-MY3National Science and Technology Council (Taiwan) NSTC 113-2640-B-005-001National Science and Technology Council (Taiwan) NSTC 114-2640-B-005-001
6 · The paper itself

Abstract

Influenza causes approximately one billion infections and hundreds of thousands of deaths each year. Occasionally, highly pathogenic new virus strains emerge. Research on emerging influenza viruses or multiple viral strains is often limited by the need for high biosafety level (BSL) laboratories. To overcome this limitation, we attempt to establish a BSL-1-compatible influenza research platform using baculovirus surface display technology. We constructed influenza virus pseudotypes HA-Bac and NA-Bac by displaying hemagglutinin (HA) and neuraminidase (NA) proteins from influenza viruses on the surface of baculoviruses. Different HA-Bac and NA-Bac induced a unique inflammatory cytokine profile after transduction into respiratory epithelial and macrophage cell lines. Using insect cells infected with these HA-Bac and NA-Bac as antigens, we established cell-based and lysate-based ELISA to detect HA and NA antibodies. The lysate-based ELISA showed excellent performance in detecting IgG antibodies in patients' serum samples. Finally, hemagglutination induced by HA-Bac-infected insect cells and neuraminidase activity generated by NA-Bac-infected cells were both inhibited by the corresponding antiviral drugs in functional inhibition assays. In summary, this study established a safe influenza research system capable of performing cytokine profiling, serological detection and antiviral drug screening under BSL-1 conditions. This system holds promise for application to other emerging respiratory viruses and support of public health preparedness.

Indexed as

Antiviral AgentsBaculoviridaeCell Surface Display TechniquesCytokinesOrthomyxoviridaeAnimalsAntibodies, ViralCell LineDrug Evaluation, PreclinicalEnzyme-Linked Immunosorbent AssayEpithelial CellsHemagglutinin Glycoproteins, Influenza VirusHumansImmunoglobulin GInsectaNeuraminidaseAntibodies, ViralAntiviral AgentsCytokinesHemagglutinin Glycoproteins, Influenza VirusImmunoglobulin GNeuraminidaseantiviral molecule screeningbaculoviruscytokine profileinfluenzaserological detection

Identifiers

PMID42237749
PMCPMC13581098

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.