Evidence map›Paper›PMID 39422666›Full record

ArticleThe Journal of general virology2024

A broadly reactive ultralong bovine antibody that can determine the integrity of foot-and-mouth disease virus capsids.

John D Clarke, Helen M E Duyvesteyn, Eva Perez-Martin, Undīne Latišenko, Claudine Porta, Kathleen V Humphreys, Abigail L Hay, Jingshan Ren, Elizabeth E Fry, Erwin van den Born and 5 more

Abstract read
In one paragraph

Article in The Journal of general virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

John D ClarkeThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Helen M E DuyvesteynThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Eva Perez-MartinThe Pirbright Institute, Woking, GU24 0NF, UK.
Undīne LatišenkoMSD Animal Health, 5831 AN Boxmeer, Netherlands.
Claudine PortaThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Kathleen V HumphreysThe Pirbright Institute, Woking, GU24 0NF, UK.
Abigail L HayThe Pirbright Institute, Woking, GU24 0NF, UK.
Jingshan RenThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Elizabeth E FryThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Erwin van den BornMSD Animal Health, 5831 AN Boxmeer, Netherlands.
Bryan CharlestonThe Pirbright Institute, Woking, GU24 0NF, UK.
Marie Bonnet-Di PlacidoThe Pirbright Institute, Woking, GU24 0NF, UK.
Raymond J OwensThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
David I StuartThe Division of Structural Biology, Nuffield Department of Medicine, The Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
John A HammondThe Pirbright Institute, Woking, GU24 0NF, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Foot-and-mouth disease vaccination using inactivated virus is suboptimal, as the icosahedral viral capsids often disassemble into antigenically distinct pentameric units during long-term storage, or exposure to elevated temperature or lowered pH, and thus raise a response that is no longer protective. Furthermore, as foot-and-mouth disease virus (FMDV)'s seven serotypes are antigenically diverse, cross-protection from a single serotype vaccine is limited, and most existing mouse and bovine antibodies and camelid single-domain heavy chain-only antibodies are serotype-specific. For quality control purposes, there is a real need for pan-serotype antibodies that clearly distinguish between pentamer (12S) and protective intact FMDV capsid. To date, few cross-serotype bovine-derived antibodies have been reported in the literature. We identify a bovine antibody with an ultralong CDR-H3, Ab117, whose structural analysis reveals that it binds to a deep, hydrophobic pocket on the interior surface of the capsid via the CDR-H3. Main-chain and hydrophobic interactions provide broad serotype specificity. ELISA analysis confirms that Ab117 is a novel pan-serotype and conformational epitope-specific 12S reagent, suitable for assessing capsid integrity.

Indexed as

Antibodies, ViralCapsidCapsid ProteinsFoot-and-Mouth Disease VirusAnimalsCattleCross ReactionsEpitopesFoot-and-Mouth DiseaseSerogroupAntibodies, ViralCapsid ProteinsEpitopesFMDVpan-specificsingle particle analysisultralong CDR antibodyvaccine quality assurance

Identifiers

PMID39422666
PMCPMC11488517

What OpenQuestion holds

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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.