Evidence map›Paper›PMID 39380504›Full record

ArticleBiotechnology journal2024

Single-Batch Expression of an Experimental Recombinant Snakebite Antivenom Based on an Oligoclonal Mixture of Human Monoclonal Antibodies.

Anna C Adams, Lise M Grav, Shirin Ahmadi, Camilla Holst Dahl, Anne Ljungars, Andreas H Laustsen, Lars K Nielsen

Abstract read
In one paragraph

Article in Biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Novel antivenoms bite back.Nature biotechnology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Comment on: What is new in the treatment of snakebite envenoming? Opportunities and challenges.Transactions of the Royal Society of Tropical Medicine and Hygiene · 2025
    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

7 authors.

Anna C AdamsCenter for Biosustainability, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0009-0007-3127-9701
Lise M GravDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0000-0001-8042-7108
Shirin AhmadiDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0000-0002-4131-583X
Camilla Holst DahlDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.
Anne LjungarsDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0000-0002-2158-0601
Andreas H LaustsenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0000-0001-6918-5574
Lars K NielsenCenter for Biosustainability, Technical University of Denmark, Lyngby, Denmark.ORCID https://orcid.org/0000-0001-8191-3511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligoclonal antibodies, which are carefully defined mixtures of monoclonal antibodies, are valuable for the treatment of complex diseases, such as infectionss and cancer. In addition to these areas of medicine, they could be utilized for the treatment of snakebite envenoming, where recombinantly produced monoclonal human antibodies could overcome many of the drawbacks accompanying traditional antivenoms. However, producing multiple individual batches of monoclonal antibodies in an industrial setting is associated with significant costs. Therefore, it is attractive to produce oligoclonal antibodies by mixing multiple antibody-producing cell lines in a single batch to have only one upstream and downstream process. In this study, we selected four antibodies that target different toxins found in the venoms of various elapid snake species, such as mambas and cobras, and generated stable antibody-producing cell lines. Upon co-cultivation, we found the cell line ratios to be stable over 7 days. The purified oligoclonal antibody cocktail contained the anticipated antibody concentrations and bound to the target toxins as expected. These results thus provide a proof of concept for the strategy of mixing multiple cell lines in a single batch to manufacture tailored antivenoms recombinantly, which could be utilized for the treatment of snakebite envenoming and in other fields where oligoclonal antibody mixtures could find utility.

Indexed as

Antibodies, MonoclonalAntiveninsRecombinant ProteinsAnimalsCHO CellsCricetulusElapidaeElapid VenomsHumansSnake BitesAntibodies, MonoclonalAntiveninsElapid VenomsRecombinant Proteinsantibody mixtureantivenomcell line engineeringoligoclonal antibody expressionrecombinant antivenomsingle‐batch expressionsnakebite envenomingsnake toxinssnake venomtargeted integration

Identifiers

PMID39380504
PMCPMC7618995

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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.