Evidence map›Paper›PMID 42058010›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Unique DNA impacts on transient Expi293

Bo Hee Shin, Jing Zhou, Audrey M Vogt, Lauren Gebhardt, Molica Abel, Hamza Sahil, Fabrice Lamour, Anna Kimeu, Ian R Wallace-Moyer, Sean Lim and 3 more

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2026. 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

13 authors.

Bo Hee Shin *BioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Jing Zhou *BioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Audrey M VogtBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Lauren GebhardtBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Molica AbelBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Hamza SahilBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Fabrice LamourBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Anna KimeuBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Ian R Wallace-MoyerBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Sean LimBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Laura LinBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Aaron M D'AntonaBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.
Xiaotian ZhongBioMedicine Design, Preclinical and Translational Sciences, Pfizer Research and Development, Cambridge, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mammalian transient gene expression technology is an essential tool for biotherapeutics engineering and production. Various reported transient expression systems in human embryonic kidney (HEK) 293 or Chinese hamster ovary (CHO) cells display different expression patterns and production yields, yet the mechanisms to which these patterns and yields can be attributed remain unknown. Methods: To identify the determining factors, we have dissected the transient expression processes through a three-snapshot approach for four commercially available transient production systems: Expi293 Results: The data showed that in response to titrated amounts of transfected DNAs for both the surface-display fusion molecule and the cytosolic GFP, Expi293 Conclusion: These results together suggested that the efficiency in handling transfected DNAs for protein synthesis (i.e., the ability to make intracellularly up-taken plasmid DNA complexes competent for DNA transcription in the nucleus) is likely a key limiting factor for effective transient production.

Indexed as

Chinese hamster ovaryempty expression vectorhuman embryonic kidney 293mammalian transient gene expressionsurface-display moleculethree-snapshot approachtransfected plasmid DNA

Identifiers

PMID42058010
PMCPMC13121143

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Registered trials

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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.