Evidence map›Paper›PMID 38259154›Full record

ArticleACS synthetic biology2024

Synthetic Cell Lines for Inducible Packaging of Influenza A Virus.

Thu Phan, Qian Ye, Christopher Stach, Yu-Chieh Lin, Haoyu Cao, Annika Bowen, Ryan A Langlois, Wei-Shou Hu

Open access · greenAbstract read
In one paragraph

Article in ACS synthetic biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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 at 1 institution in 2 countries.

Thu PhanDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0001-5169-8785
Qian YeDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0001-9310-1553
Christopher StachDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Yu-Chieh LinDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Haoyu CaoDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Annika BowenDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Ryan A LangloisDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Wei-Shou HuDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0001-7739-8692
University of Minnesota · US

Funding

Early Responses to Influenza A Virus Replication In VivoR01AI148669 · NIAID · UNIVERSITY OF MINNESOTA · PI LANGLOIS, RYAN · 2020 to 2024
$2.5M
NIAID NIH HHS R01 AI148669
6 · The paper itself

Abstract

Influenza A virus (IAV) is a negative-sense RNA virus that causes seasonal infections and periodic pandemics, inflicting huge economic and human costs on society. The current production of influenza virus for vaccines is initiated by generating a seed virus through the transfection of multiple plasmids in HEK293 cells followed by the infection of seed viruses into embryonated chicken eggs or cultured mammalian cells. We took a system design and synthetic biology approach to engineer cell lines that can be induced to produce all viral components except hemagglutinin (HA) and neuraminidase (NA), which are the antigens that specify the variants of IAV. Upon the transfection of HA and NA, the cell line can produce infectious IAV particles. RNA-Seq transcriptome analysis revealed inefficient synthesis of viral RNA and upregulated expression of genes involved in host response to viral infection as potential limiting factors and offered possible targets for enhancing the productivity of the synthetic cell line. Overall, we showed for the first time that it was possible to create packaging cell lines for the production of a cytopathic negative-sense RNA virus. The approach allows for the exploitation of altered kinetics of the synthesis of viral components and offers a new method for manufacturing viral vaccines.

Indexed as

Artificial CellsInfluenza A virusInfluenza VaccinesAnimalsHEK293 CellsHemagglutinin Glycoproteins, Influenza VirusHemagglutininsHumansMammalsHemagglutinin Glycoproteins, Influenza VirusHemagglutininsInfluenza Vaccinesinfluenza A virussynthetic biologyvaccine manufacturing

Identifiers

PMID38259154
PMCPMC10878389
OpenAlexW4391144677

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.