Evidence map›Paper›PMID 38363529›Full record

ReviewMolecular biotechnology2025

From Efficiency to Yield: Exploring Recent Advances in CHO Cell Line Development for Monoclonal Antibodies.

Sarmishta Majumdar, Ranjeet Desai, Aakarsh Hans, Prajakta Dandekar, Ratnesh Jain

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Plant-Based Systems for Producing Therapeutic Proteins: Current Status and Future Prospects.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
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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

5 authors at 1 institution in 1 country.

Sarmishta MajumdarDepartment of Biological Science and Biotechnology, Institute of Chemical Technology, Mumbai, 400019, India.ORCID http://orcid.org/0009-0004-4439-0634
Ranjeet DesaiDepartment of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, 400019, India.ORCID http://orcid.org/0009-0005-1979-3455
Aakarsh HansDepartment of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, 400019, India.ORCID http://orcid.org/0009-0000-6054-3240
Prajakta DandekarDepartment of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai, 400019, India. pd.jain@ictmumbai.edu.in.ORCID http://orcid.org/0000-0001-5968-1072
Ratnesh JainDepartment of Biological Science and Biotechnology, Institute of Chemical Technology, Mumbai, 400019, India. rd.jain@ictmumbai.edu.in.
Institute of Chemical Technology · IN

Funding

Council of Scientific and Industrial Research, India 09/991(0059)/2019-EMR-IUniversity Grants Commission UGC-22-GE-MAH-F-SJSGC-10886
6 · The paper itself

Abstract

The increasing demand for biosimilar monoclonal antibodies (mAbs) has prompted the development of stable high-producing cell lines while simultaneously decreasing the time required for screening. Existing platforms have proven inefficient, resulting in inconsistencies in yields, growth characteristics, and quality features in the final mAb products. Selecting a suitable expression host, designing an effective gene expression system, developing a streamlined cell line generation approach, optimizing culture conditions, and defining scaling-up and purification strategies are all critical steps in the production of recombinant proteins, particularly monoclonal antibodies, in mammalian cells. As a result, an active area of study is dedicated to expression and optimizing recombinant protein production. This review explores recent breakthroughs and approaches targeted at accelerating cell line development to attain efficiency and consistency in the synthesis of therapeutic proteins, specifically monoclonal antibodies. The primary goal is to bridge the gap between rising demand and consistent, high-quality mAb production, thereby benefiting the healthcare and pharmaceutical industries.

Indexed as

Antibodies, MonoclonalCricetulusRecombinant ProteinsAnimalsBiosimilar PharmaceuticalsCell Culture TechniquesCHO CellsHumansAntibodies, MonoclonalBiosimilar PharmaceuticalsRecombinant ProteinsBiosimilarsCell line developmentCHOExpression vectorGenetic engineering

Identifiers

PMID38363529
OpenAlexW4391879502

What OpenQuestion holds

Textmetadata
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.