Evidence map›Paper›PMID 34417258›Full record

ArticleScience immunology2021

A high-affinity human TCR-like antibody detects celiac disease gluten peptide-MHC complexes and inhibits T cell activation.

Rahel Frick, Lene S Høydahl, Jan Petersen, M Fleur du Pré, Shraddha Kumari, Grete Berntsen, Alisa E Dewan, Jeliazko R Jeliazkov, Kristin S Gunnarsen, Terje Frigstad and 10 more

Open access · greenAbstract read
In one paragraph

Article in Science immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Coeliac disease: complications and comorbidities.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. A general platform for targeting MHC-II antigens via a single loop.bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Article
  12. Celiac disease: mechanisms and emerging therapeutics.Trends in pharmacological sciences · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

20 authors at 6 institutions in 4 countries.

Rahel FrickCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0002-3469-5686
Lene S HøydahlCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0001-6070-1413
Jan PetersenInfection and Immunity Program, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-2045-6342
M Fleur du PréCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Shraddha KumariNextera AS, Oslo, Norway.
Grete BerntsenNextera AS, Oslo, Norway.ORCID 0000-0002-8920-9200
Alisa E DewanCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0001-7314-5778
Jeliazko R JeliazkovProgram in Molecular Biophysics, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0003-4249-1955
Kristin S GunnarsenCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0002-1124-5535
Terje FrigstadNextera AS, Oslo, Norway.
Erik S VikNextera AS, Oslo, Norway.
Carmen LlerenaInfection and Immunity Program, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Knut E A LundinCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0003-1713-5545
Sheraz YaqubDepartment of Gastrointestinal Surgery, Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0002-5696-2319
Jørgen JahnsenInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-0419-2914
Jeffrey J GrayProgram in Molecular Biophysics, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-6380-2324
Jamie RossjohnInfection and Immunity Program, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-2020-7522
Ludvig M SollidCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.ORCID 0000-0001-8860-704X
Inger SandlieCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Geir Åge LøsetCentre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital-Rikshospitalet, Oslo, Norway. galoset@nextera.no.ORCID 0000-0002-5257-8571
Oslo University Hospital · NONextera (Norway) · NOAustralian Research Council · AUJohns Hopkins University · USAustralian Regenerative Medicine Institute · AUUniversity of Oslo · NO

Funding

Prediction of the Structure of Therapeutic Antibodies with their AntigensR01GM078221 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GRAY, JEFFREY J · 2006 to 2020
$4.0M
NIGMS NIH HHS R01 GM078221
6 · The paper itself

Abstract

Antibodies specific for peptides bound to human leukocyte antigen (HLA) molecules are valuable tools for studies of antigen presentation and may have therapeutic potential. Here, we generated human T cell receptor (TCR)-like antibodies toward the immunodominant signature gluten epitope DQ2.5-glia-α2 in celiac disease (CeD). Phage display selection combined with secondary targeted engineering was used to obtain highly specific antibodies with picomolar affinity. The crystal structure of a Fab fragment of the lead antibody 3.C11 in complex with HLA-DQ2.5:DQ2.5-glia-α2 revealed a binding geometry and interaction mode highly similar to prototypic TCRs specific for the same complex. Assessment of CeD biopsy material confirmed disease specificity and reinforced the notion that abundant plasma cells present antigen in the inflamed CeD gut. Furthermore, 3.C11 specifically inhibited activation and proliferation of gluten-specific CD4

Indexed as

AnimalsCD4-Positive T-LymphocytesCeliac DiseaseCell Line, TumorEpitopes, T-LymphocyteGlutensHLA-DQ AntigensHumansLymphocyte ActivationMiceModels, MolecularPeptidesReceptors, Antigen, T-CellEpitopes, T-LymphocyteGlutensHLA-DQ2 antigenHLA-DQ AntigensPeptidesReceptors, Antigen, T-Cell

Identifiers

PMID34417258
PMCPMC8670751
OpenAlexW3193681478

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.