Evidence map›Paper›PMID 41501035›Full record

ArticleNature communications2026

Protection against lethal canine distemper virus infection by a dual epitope-targeting synthetic antibody.

Melanie Scherer, Nadia Djabeur, Oliver Siering, Jean-Marc Jeckelmann, Marianne Wyss, Marina Cresci, Morgane Di Palma Subran, Rainer Riedl, Patrick Chames, Christian K Pfaller and 3 more

Abstract read
In one paragraph

Article in Nature communications, 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.

Melanie Scherer *Division of Neurological Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-5554-9664
Nadia Djabeur *Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
Oliver Siering *Division of Veterinary Medicine, Paul-Ehrlich-Institute, Langen, Germany.
Jean-Marc JeckelmannInstitute of Biochemistry and Molecular Medicine, Medical Faculty, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-9973-2700
Marianne WyssDivision of Neurological Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Marina CresciAix-Marseille Université, CNRS, INSERM, Institute Paoli-Calmettes, CRCM, Marseille, France.
Morgane Di Palma SubranAix-Marseille Université, CNRS, INSERM, Institute Paoli-Calmettes, CRCM, Marseille, France.
Rainer RiedlCompetence Center for Drug Discovery, ZHAW Zurich University of Applied Sciences, Institute of Chemistry and Biotechnology, Wädenswil, Switzerland.ORCID http://orcid.org/0000-0003-2534-1963
Patrick ChamesAix-Marseille Université, CNRS, INSERM, Institute Paoli-Calmettes, CRCM, Marseille, France.ORCID http://orcid.org/0000-0002-6104-6286
Christian K PfallerDivision of Veterinary Medicine, Paul-Ehrlich-Institute, Langen, Germany.ORCID http://orcid.org/0000-0003-3302-0780
Bevan SawatskyDivision of Veterinary Medicine, Paul-Ehrlich-Institute, Langen, Germany. bevan.sawatsky@pei.de.ORCID http://orcid.org/0000-0001-6908-1556
Dimitrios FotiadisInstitute of Biochemistry and Molecular Medicine, Medical Faculty, University of Bern, Bern, Switzerland. dimitrios.fotiadis@unibe.ch.ORCID http://orcid.org/0000-0001-9682-7931
Philippe PlattetDivision of Neurological Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland. philippe.plattet@unibe.ch.ORCID http://orcid.org/0000-0003-3313-2598

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) CRC 1021 Project 197785619/B12Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 310030_204363Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) CRSII5_183481
6 · The paper itself

Abstract

Despite vaccine availability, the morbilliviruses measles virus and canine distemper virus (CDV) are still causing major health impairments in human and animal populations. Here, we identified two potent, neutralizing single domain antibodies directed against the tetrameric receptor binding (H) protein of CDV. Structural analyses spotlighted two vulnerable sites within the H protein. While the first overlaps with the receptor binding site, the second encompasses amino acid residues of two protomers located at the distal dimeric head interface, which supports distinct mechanisms of neutralization. Upon application of an engineered tetravalent and biparatopic antibody, ferrets were protected at a remarkably low antibody dose (1 mg/kg) administered intra-peritoneally on days 3 and 7 post-exposure of a lethal CDV challenge. Collectively, this study spotlights the power of integrating multiple mechanisms of neutralization in a single format and provides a roadmap to design next-generation therapeutics against morbilliviral infections as well as other infectious pathogens.

Indexed as

Antibodies, NeutralizingAntibodies, ViralDistemperDistemper Virus, CanineEpitopesSingle-Domain AntibodiesAnimalsDogsFemaleFerretsHumansNeutralization TestsAntibodies, NeutralizingAntibodies, ViralEpitopesSingle-Domain Antibodies

Identifiers

PMID41501035
PMCPMC12780139

What OpenQuestion holds

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LicenceCC BY
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.