Evidence map›Paper›PMID 38773068›Full record

ArticleNature communications2024

In vivo neutralization of coral snake venoms with an oligoclonal nanobody mixture in a murine challenge model.

Melisa Benard-Valle, Yessica Wouters, Anne Ljungars, Giang Thi Tuyet Nguyen, Shirin Ahmadi, Tasja Wainani Ebersole, Camilla Holst Dahl, Alid Guadarrama-Martínez, Frederikke Jeppesen, Helena Eriksen and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Multiobjective VScience advances · 2026
    Article
  2. Review
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  4. Generalizable Direct Protein Sequencing With InstaNexus.Molecular & cellular proteomics : MCP · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. 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
  13. Article
  14. Article
  15. Article
  16. Microbes Saving Lives and Reducing Suffering.Microbial biotechnology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. 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

18 authors.

Melisa Benard-ValleDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0002-0042-6592
Yessica WoutersDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Anne LjungarsDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0002-2158-0601
Giang Thi Tuyet NguyenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0002-3536-9903
Shirin AhmadiDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Tasja Wainani EbersoleDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Camilla Holst DahlDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Alid Guadarrama-MartínezDepartamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Avenida Universidad 2001, Cuernavaca, Mor, 62210, México.ORCID http://orcid.org/0009-0007-6378-0859
Frederikke JeppesenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Helena EriksenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0009-0000-7850-4960
Gibran Rodríguez-BarreraDepartamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Avenida Universidad 2001, Cuernavaca, Mor, 62210, México.ORCID http://orcid.org/0009-0004-6969-8360
Kim BoddumSophion Bioscience, DK-2750, Ballerup, Denmark.ORCID http://orcid.org/0000-0002-1588-9055
Timothy Patrick JenkinsDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.ORCID http://orcid.org/0000-0003-2979-5663
Sara Petersen BjørnDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Sanne SchoffelenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Bjørn Gunnar VoldborgDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark.
Alejandro AlagónDepartamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Avenida Universidad 2001, Cuernavaca, Mor, 62210, México.
Andreas Hougaard LaustsenDepartment of Biotechnology and Biomedicine, Technical University of Denmark, DK-2800, Kongens, Lyngby, Denmark. ahola@bio.dtu.dk.ORCID http://orcid.org/0000-0001-6918-5574

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 713683EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 850974EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 899987Novo Nordisk Fonden (Novo Nordisk Foundation) NNF20SA0066621Villum Fonden (Villum Foundation) 00025302Wellcome TrustWellcome Trust (Wellcome) 221702/Z/20/Z
6 · The paper itself

Abstract

Oligoclonal mixtures of broadly-neutralizing antibodies can neutralize complex compositions of similar and dissimilar antigens, making them versatile tools for the treatment of e.g., infectious diseases and animal envenomations. However, these biotherapeutics are complicated to develop due to their complex nature. In this work, we describe the application of various strategies for the discovery of cross-neutralizing nanobodies against key toxins in coral snake venoms using phage display technology. We prepare two oligoclonal mixtures of nanobodies and demonstrate their ability to neutralize the lethality induced by two North American coral snake venoms in mice, while individual nanobodies fail to do so. We thus show that an oligoclonal mixture of nanobodies can neutralize the lethality of venoms where the clinical syndrome is caused by more than one toxin family in a murine challenge model. The approaches described may find utility for the development of advanced biotherapeutics against snakebite envenomation and other pathologies where multi-epitope targeting is beneficial.

Indexed as

Antibodies, NeutralizingCoral SnakesSingle-Domain AntibodiesAnimalsAntiveninsCell Surface Display TechniquesDisease Models, AnimalElapid VenomsEpitopesFemaleMiceMice, Inbred BALB CSnake BitesAntibodies, NeutralizingAntiveninsElapid VenomsEpitopesSingle-Domain Antibodies

Identifiers

PMID38773068
PMCPMC11109316

What OpenQuestion holds

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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.