Evidence map›Paper›PMID 35767011›Full record

ArticleApplied microbiology and biotechnology2022

Cell-line screening and process development for a fusogenic oncolytic virus in small-scale suspension cultures.

Sven Göbel, Fabian Kortum, Karim Jaén Chavez, Ingo Jordan, Volker Sandig, Udo Reichl, Jennifer Altomonte, Yvonne Genzel

Open access · hybridAbstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 18 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 3 institutions in 1 country.

Sven GöbelMax Planck Institute for Dynamics of Complex Technical Systems, Bioprocess Engineering, Sandtorstr. 1, 39106, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-2264-5569
Fabian KortumDepartment of Internal Medicine II, Klinikum Rechts Der Isar, Technische Universität München, Munich, Germany.ORCID http://orcid.org/0000-0003-1387-1350
Karim Jaén ChavezDepartment of Internal Medicine II, Klinikum Rechts Der Isar, Technische Universität München, Munich, Germany.ORCID http://orcid.org/0000-0001-7129-8797
Ingo JordanProBioGen AG, Herbert-Bayer-Str. 8, 13086, Berlin, Germany.ORCID http://orcid.org/0000-0003-2711-7252
Volker SandigProBioGen AG, Herbert-Bayer-Str. 8, 13086, Berlin, Germany.
Udo ReichlMax Planck Institute for Dynamics of Complex Technical Systems, Bioprocess Engineering, Sandtorstr. 1, 39106, Magdeburg, Germany.ORCID http://orcid.org/0000-0001-6538-1332
Jennifer AltomonteDepartment of Internal Medicine II, Klinikum Rechts Der Isar, Technische Universität München, Munich, Germany.ORCID http://orcid.org/0000-0003-1079-3633
Yvonne GenzelMax Planck Institute for Dynamics of Complex Technical Systems, Bioprocess Engineering, Sandtorstr. 1, 39106, Magdeburg, Germany. genzel@mpi-magdeburg.mpg.de.ORCID http://orcid.org/0000-0002-2652-5943
Max Planck Institute for Dynamics of Complex Technical Systems · DETUM Klinikum · DEBayer (Germany) · DE

Funding

Bundesministerium für Wirtschaft und Energie #03EFOBY215
6 · The paper itself

Abstract

Oncolytic viruses (OVs) represent a novel class of immunotherapeutics under development for the treatment of cancers. OVs that express a cognate or transgenic fusion protein is particularly promising as their enhanced intratumoral spread via syncytia formation can be a potent mechanism for tumor lysis and induction of antitumor immune responses. Rapid and efficient fusion of infected cells results in cell death before high titers are reached. Although this is an attractive safety feature, it also presents unique challenges for large-scale clinical-grade manufacture of OVs. Here we evaluate the use of four different suspension cell lines for the production of a novel fusogenic hybrid of vesicular stomatitis virus and Newcastle disease virus (rVSV-NDV). The candidate cell lines were screened for growth, metabolism, and virus productivity. Permissivity was evaluated based on extracellular infectious virus titers and cell-specific virus yields (CSVYs). For additional process optimizations, virus adaptation and multiplicity of infection (MOI) screenings were performed and confirmed in a 1 L bioreactor. BHK-21 and HEK293SF cells infected at concentrations of 2 × 10

Indexed as

NeoplasmsOncolytic VirotherapyOncolytic VirusesAnimalsCell LineNewcastle disease virusVirus CultivationVirus ReplicationCell culture-based productionCell line screeningFusogenic oncolytic virusUpstream processing

Identifiers

PMID35767011
PMCPMC9329169
OpenAlexW4283705226

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.