Evidence map›Paper›PMID 41927489›Full record

ArticleBiotechnology progress

An efficient and robust strategy for developing cell lines through targeted integration.

Duncan McVey, Charu Garg, Chaojie Wang, Aashir Awan, Rui Zheng, Jennifer Zhang, Steve Sturner, Erik Langsdorf, Le Yu, Krishnamurthy Shankarling and 4 more

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. 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
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.

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

14 authors.

Duncan McVeyBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.ORCID 0000-0002-1441-1973
Charu GargBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Chaojie WangBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Aashir AwanBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Rui ZhengBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Jennifer ZhangBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Steve SturnerBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Erik LangsdorfBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Le YuBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Krishnamurthy ShankarlingBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Giovanni RizziBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Kitty AgarwalBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Gabi TremmlBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.
Anurag KhetanBiologics Development, Bristol Myers Squibb, New Brunswick, New Jersey, USA.ORCID 0000-0001-6408-6155

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reducing the time needed and enhancing predictability of outcomes for cell line development is an ongoing focus of improvement. Targeted integration (TI) where the expression cassettes for a biologic are inserted at a predefined locus, a landing pad, is one of the strategies that is used for this purpose. To be commercially viable the landing pad host cell must support high titers and the transgenes in the landing pad must be highly transcribed. To make such a host TI cell line takes a great deal of time and effort with little guarantee of success. Here we describe a strategy where we converted a stable high-expressing mAb cell line and generated multiple TI host cell lines that are commercially relevant. We routinely generate 6 g/L mAb clones using our platform fit process and 8 to >10 g/L with process optimization that are phenotypically and genetically stable. We also created a duo-landing pad where both landing pads reside in the same locus. This gives the opportunity to simplify the construction of differentially expressed genes since both landing pads are expected to perform equally.

Indexed as

Antibodies, MonoclonalCell LineAnimalsHumansTransgenesAntibodies, Monoclonal

Identifiers

PMID41927489
PMCPMC13441354

What OpenQuestion holds

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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.