Evidence map›Paper›PMID 31651085›Full record

ArticleInfluenza and other respiratory viruses2020

Comparison of suspension MDCK cells, adherent MDCK cells, and LLC-MK2 cells for selective isolation of influenza viruses to be used as vaccine seeds.

Yuichi Harada, Hitoshi Takahashi, Heidi Trusheim, Bernhard Roth, Katsumi Mizuta, Asumi Hirata-Saito, Teruko Ogane, Takato Odagiri, Masato Tashiro, Norio Yamamoto

Open access · goldAbstract read
In one paragraph

Article in Influenza and other respiratory viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 5 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

10 authors at 5 institutions in 2 countries.

Yuichi HaradaInfluenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Hitoshi TakahashiInfluenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Heidi TrusheimNovartis Vaccines and Diagnostics GmbH, Marburg, Germany.
Bernhard RothNovartis Vaccines and Diagnostics GmbH, Marburg, Germany.
Katsumi MizutaYamagata Prefectural Institute of Public Health, Yamagata, Japan.
Asumi Hirata-SaitoTochigi Prefectural Institute of Public Health and Environmental Science, Utsunomiya, Japan.
Teruko OganeTochigi Prefectural Institute of Public Health and Environmental Science, Utsunomiya, Japan.
Takato OdagiriInfluenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Masato TashiroInfluenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Norio YamamotoInfluenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan.ORCID 0000-0002-5574-1960
National Institute of Infectious Diseases · JPNovartis (Germany) · DETochigi Prefectural Police · JPJuntendo University · JPYamagata Prefectural Institute of Public Health · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell-based influenza vaccines can solve the problem of the frequent occurrence of egg adaptation-associated antigenic changes observed in egg-based vaccines. Seed viruses for cell-based vaccines can be prepared from clinical specimens by cell culture; however, clinical samples risk harboring respiratory viruses other than influenza virus. Therefore, it is necessary to investigate the patterns of co-infection in clinical samples and explore whether cell culture technology can selectively propagate influenza viruses from samples containing other respiratory viruses.

methodsA total of 341 clinical specimens were collected from patients with influenza or influenza-like illness and analyzed by ResPlex II assay to detect 18 respiratory viruses. The patterns of co-infection were statistically analyzed with Fisher's exact test. The samples with double or triple infections were passaged in suspension MDCK cells (MDCK-S), adherent MDCK cells (MDCK-A), and LLC-MK2D cells. Cell-passaged samples were analyzed by ResPlex II assay again to investigate whether each cell line could amplify influenza viruses and eliminate other respiratory viruses.

resultsDouble infections were detected in 8.5% and triple infections in 0.9% of the collected clinical specimens. We identified four pairs of viruses with significant correlation. For all samples with double and triple infection, MDCK-S and MDCK-A could selectively propagate influenza viruses, while eliminating all contaminating viruses. In contrast, LLC-MK2D showed lower isolation efficiency for influenza virus and higher isolation efficiency for coxsackievirus/echovirus than MDCK-S and MDCK-A.

conclusionsBoth MDCK-S and MDCK-A are considered suitable for the preparation of influenza vaccine seed viruses without adventitious agents or egg-adaptation mutations.

Indexed as

AnimalsCell LineDogsHumansMadin Darby Canine Kidney CellsOrthomyxoviridaeViral VaccinesVirus CultivationViral Vaccinesadventitious viruscell-based vaccineinfluenzaMadin-Darby canine kidney cell linevaccine seed virus

Identifiers

PMID31651085
PMCPMC7040968
OpenAlexW2981424994

What OpenQuestion holds

Textmetadata
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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.