Evidence map›Paper›PMID 39286892›Full record

ArticleBiotechnology progress

Fed-batch strategies for intensified rVSV vector production in high cell density cultures of suspension HEK293 cells.

Cristina A T Silva, Amine A Kamen, Olivier Henry

Abstract read
In one paragraph

Article in Biotechnology progress. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Article
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

3 authors.

Cristina A T SilvaDepartment of Chemical Engineering, Polytechnique Montréal, Montreal, Quebec, Canada.ORCID 0000-0003-1714-3975
Amine A KamenDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.ORCID 0000-0001-9110-8815
Olivier HenryDepartment of Chemical Engineering, Polytechnique Montréal, Montreal, Quebec, Canada.ORCID 0000-0003-2106-1331

Funding

Canadian Foundation for Innovation PN-40977Fonds de recherche du Québec - Nature et technologies PR-300890Natural Sciences and Engineering Research Council of Canada
6 · The paper itself

Abstract

Vesicular stomatitis virus (VSV) has been increasingly demonstrated as a promising viral vector platform. As the interest over this modality for vaccine and gene therapy applications increases, the need for intensified processes to produce these vectors emerge. In this study, we develop fed-batch-based operations to intensify the production of a recombinant VSV-based vaccine candidate (rVSV-SARS-CoV-2) in suspension cultures of HEK293 cells. A feeding strategy, in which a commercial concentrated medium was added to cultures based on cell growth through a fixed cell specific feeding rate (CSFR), was applied for the development of two different processes using Ambr250 modular bioreactors. Cultures operated in hybrid fed-batch/perfusion (FB/P) or fed-batch (FB) were able to sustain infections performed at 8.0 × 10

Indexed as

Batch Cell Culture TechniquesGenetic VectorsSARS-CoV-2BioreactorsHEK293 CellsHumansVirus Cultivationfed‐batchHEK293 cellshigh cell densityprocess intensificationsuspension cellsviral vector

Identifiers

PMID39286892
PMCPMC11831413

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.