Evidence map›Paper›PMID 24975811›Full record

ArticleVaccine2014

Performance characteristics of qualified cell lines for isolation and propagation of influenza viruses for vaccine manufacturing.

Ruben O Donis, Influenza Cell Culture Working Group, C Todd Davis, Angie Foust, M Jaber Hossain, Adam Johnson, Alexander Klimov, Rosette Loughlin, Xiyan Xu, Theodore Tsai and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 62 citations in OpenAlex.

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  19. Evidence of Influenza A in Wild Norway Rats (Frontiers in ecology and evolution · 2019
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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

24 authors at 6 institutions in 7 countries.

Ruben O Donis
Influenza Cell Culture Working Group
C Todd Davis
Angie Foust
M Jaber Hossain
Adam Johnson
Alexander Klimov
Rosette Loughlin
Xiyan Xu
Theodore Tsai
Simone Blayer
Heidi Trusheim
Tony Colegate
John Fox
Beverly Taylor
Althaf Hussain
Ian Barr
Chantal Baas
Jaap Louwerens
Ed Geuns
Min-Shi Lee
Odewijk Venhuizen
Elisabeth Neumeier
Thedi Ziegler
Centers for Disease Control and Prevention · USNovartis (United Kingdom) · GBVictorian Infectious Diseases Reference Laboratory · AUAbbott (Netherlands) · NLFinnish Institute for Health and Welfare · FINovartis (Germany) · DE

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Cell culture is now available as a method for the production of influenza vaccines in addition to eggs. In accordance with currently accepted practice, viruses recommended as candidates for vaccine manufacture are isolated and propagated exclusively in hens' eggs prior to distribution to manufacturers. Candidate vaccine viruses isolated in cell culture are not available to support vaccine manufacturing in mammalian cell bioreactors so egg-derived viruses have to be used. Recently influenza A (H3N2) viruses have been difficult to isolate directly in eggs. As mitigation against this difficulty, and the possibility of no suitable egg-isolated candidate viruses being available, it is proposed to consider using mammalian cell lines for primary isolation of influenza viruses as candidates for vaccine production in egg and cell platforms. To investigate this possibility, we tested the antigenic stability of viruses isolated and propagated in cell lines qualified for influenza vaccine manufacture and subsequently investigated antigen yields of such viruses in these cell lines at pilot-scale. Twenty influenza A and B-positive, original clinical specimens were inoculated in three MDCK cell lines. The antigenicity of recovered viruses was tested by hemagglutination inhibition using ferret sera against contemporary vaccine viruses and the amino acid sequences of the hemagglutinin and neuraminidase were determined. MDCK cell lines proved to be highly sensitive for virus isolation. Compared to the virus sequenced from the original specimen, viruses passaged three times in the MDCK lines showed up to 2 amino acid changes in the hemagglutinin. Antigenic stability was also established by hemagglutination inhibition titers comparable to those of the corresponding reference virus. Viruses isolated in any of the three MDCK lines grew reasonably well but variably in three MDCK cells and in VERO cells at pilot-scale. These results indicate that influenza viruses isolated in vaccine certified cell lines may well qualify for use in vaccine production.

Indexed as

Antigenic VariationVirus CultivationAnimalsAntigens, ViralChlorocebus aethiopsDogsFerretsHemagglutination Inhibition TestsInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeMadin Darby Canine Kidney CellsOrthomyxoviridaeVero CellsAntigens, ViralAntigenic stabilityGenetic stabilityInfluenza vaccinesMDCKVaccine-certified cell linesVEROVirus isolationVirus purification

Identifiers

PMID24975811
PMCPMC5915289
OpenAlexW2110607810

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.