Evidence map›Paper›PMID 32723833›Full record

ArticleRMD open2020

Dual neutralisation of IL-17F and IL-17A with bimekizumab blocks inflammation-driven osteogenic differentiation of human periosteal cells.

Mittal Shah, Asher Maroof, Panos Gikas, Gayatri Mittal, Richard Keen, Dominique Baeten, Stevan Shaw, Scott J Roberts

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Osteoimmunology of Spondyloarthritis.International journal of molecular sciences · 2023
    Review
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

8 authors at 3 institutions in 1 country.

Mittal ShahUCB Pharma, Slough, UK.
Asher MaroofUCB Pharma, Slough, UK.
Panos GikasRoyal National Orthopaedic Hospital Stanmore, Stanmore, UK.
Gayatri MittalRoyal National Orthopaedic Hospital Stanmore, Stanmore, UK.
Richard KeenRoyal National Orthopaedic Hospital Stanmore, Stanmore, UK.
Dominique BaetenUCB Pharma, Slough, UK.
Stevan ShawUCB Pharma, Slough, UK.
Scott J RobertsUCB Pharma, Slough, UK scott.roberts@ucl.ac.uk.ORCID 0000-0003-3974-8895
UCB Pharma (United Kingdom) · GBRoyal National Orthopaedic Hospital · GBRoyal Veterinary College · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInterleukin (IL)-17 signalling has been shown to be a key regulator of disease in ankylosing spondylitis (AS) with several IL-17 blockers currently clinically approved. Despite this, the role of IL-17 in bone pathology is poorly understood. This study aimed to investigate IL-17 signalling in the context of pathological bone formation.

methodsA biomimetic human periosteum-derived cell (hPDC) model of osteogenic differentiation was used in combination with recombinant IL-17 cytokines, T-cell supernatants or serum from patients with AS. IL-17A, IL-17F and bimekizumab monoclonal antibodies were used to block IL-17 cytokine action.

resultsRecombinant IL-17A and IL-17F are pro-osteogenic with respect to hPDC differentiation. T helper 17 or γδ-T cell supernatants also potently stimulated in vitro bone formation, which was blocked deeper by dual inhibition of IL-17A and IL-17F than by neutralisation of IL-17A or IL-17F individually. Osteogenic blockade may be due to an increase in expression of the Wnt antagonist

conclusionsThese data show for the first time that IL-17A and IL-17F enhance in vitro osteogenic differentiation and bone formation from hPDCs, inhibition of which may offer an attractive therapeutic strategy to prevent pathological bone formation.

Indexed as

Antibodies, Monoclonal, HumanizedAntibodies, NeutralizingBone MatrixCalcification, PhysiologicCell DifferentiationCytokinesHumansInterleukin-17OsteogenesisPeriosteumReceptors, Antigen, T-Cell, gamma-deltaReceptors, InterleukinReceptors, Interleukin-17Th17 CellsAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingbimekizumabCytokinesIL17A protein, humanIL17F protein, humanIL17RA protein, humanIL17RC protein, humanInterleukin-17Receptors, Antigen, T-Cell, gamma-deltaReceptors, InterleukinReceptors, Interleukin-17Ankylosing SpondylitisCytokinesInflammationTCells

Identifiers

PMID32723833
PMCPMC7722278
OpenAlexW3045768231

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.