Evidence map›Paper›PMID 40700293›Full record

ArticleAntibodies (Basel, Switzerland)2025

Impact of Light-Chain Variants on the Expression of Therapeutic Monoclonal Antibodies in HEK293 and CHO Cells.

Alexander Veber, Dennis Lenau, Polyniki Gkragkopoulou, David Kornblüh Bauer, Ingo Focken, Wulf Dirk Leuschner, Christian Beil, Sandra Weil, Ercole Rao, Thomas Langer

Abstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Alexander VeberSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Dennis LenauSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Polyniki GkragkopoulouSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
David Kornblüh BauerSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Ingo FockenSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Wulf Dirk LeuschnerSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Christian BeilSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Sandra WeilSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Ercole RaoSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.
Thomas LangerSanofi-Aventis Deutschland GmbH, R&D Large Molecules Research, Industriepark Höchst, 65926 Frankfurt am Main, Germany.ORCID 0000-0002-4012-3051

Funding

Sanofi-Aventis Deutschland GmbH na
6 · The paper itself

Abstract

Recombinantly produced monoclonal antibodies (mabs) belong to the fastest growing class of biotherapeutics. In humans, antibodies are classified into five different classes: IgA, IgD, IgE, IgG and IgM. Most of the therapeutic mabs used in the clinic belong to the IgG class, albeit other antibody classes, e.g., IgM, have been evaluated in clinical stages. Antibodies are composed of heavy chains paired with a light chain. In IgM and IgA, an additional chain, the J-chain, is present. Two types of light chains exist in humans: the κ-light chain and the λ-light chain. The κ-light chain predominates in humans and is used in the vast majority of therapeutic IgG. The reason for the preference of the κ-light chain in humans is not known. Our study investigates whether light-chain selection influences the productivity of the clinically validated mabs adalimumab and trastuzumab. Both mabs were expressed as IgG and IgM with a κ- or a λ-light chain in HEK293 cells. Besides comparing the expression levels of the different mabs, we also evaluated whether the passage number of the cell line has an impact on product yield. In addition, the expressions of adalimumab, trastuzumab, an anti-CD38 and an anti-PD-L1-antibody were analyzed in HEK293 and CHO cells when both the κ- and λ-light chains are present. In summary, IgG outperformed IgM variants in expression efficacy, while light-chain selection had minimal impact on the overall expression levels. The yields of all mab variants were higher in fresh cells, despite cell cultures with a high cell passage number having higher cell densities and cell numbers at the time of harvest. The incorporation of a particular light chain occurred at similar rates in HEK293 and CHO cells.

Indexed as

CHO cellsHEK cellsImmunoglobulin G (IgG)Immunoglobulin M (IgM)Kappa and Lambda light chainrecombinant expression

Identifiers

PMID40700293
PMCPMC12286288

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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.