Evidence map›Paper›PMID 38543924›Full record

ArticleVaccines2024

MDCK-Adaptive Mutation of A169S Changes Glycosylation Pattern of Hemagglutinin and Enhances MDCK-Based H7N9 Vaccine Virus Production without Loss of Antigenicity and Immunogenicity.

Po-Ling Chen, Tsai-Chuan Weng, Chia-Chun Lai, Tsai-Teng Tzeng, Min-Han Lin, Kai-Chieh Hu, Alan Yung-Chih Hu, Min-Shi Lee, Wang-Chou Sung

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2024. 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, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

9 authors at 1 institution in 1 country.

Po-Ling ChenNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Tsai-Chuan WengNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.ORCID 0000-0002-8609-9253
Chia-Chun LaiNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Tsai-Teng TzengNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Min-Han LinNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Kai-Chieh HuNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Alan Yung-Chih HuNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Min-Shi LeeNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.
Wang-Chou SungNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan 350, Taiwan.ORCID 0000-0002-3445-6036
National Health Research Institutes · TW

Funding

Ministry of Science and Technology, Taiwan MOST 109-2327-B-400-005National Health Research Institutes, Taiwan IV-110-PP-17
6 · The paper itself

Abstract

The adaptation of egg-derived H7N9 candidate vaccine virus (CVV) in the mammalian cell line is an approach to developing a high-growth virus strain for the mass production of vaccine manufacturing. The adaptive mutations that occur in hemagglutinin (HA) are critical to the activity and potency of the vaccine virus. Previously, we identified a new mutation of A169S in the HA protein of an MDCK-adapted H7N9 vaccine virus (A/Anhui/2013, RG268); however, whether and how this mutation affects vaccine potency remain to be investigated. In this study, we serially passaged RG268 in MDCK cells and found that the HA titer and the TCID

Indexed as

adaptive mutationcandidate vaccine virusglycosylationH7N9MDCK

Identifiers

PMID38543924
PMCPMC10974521
OpenAlexW4392652719

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.