Evidence map›Paper›PMID 30417018›Full record

ArticleJournal of immunology research2018

Anti-ICOSL New Antigen Receptor Domains Inhibit T Cell Proliferation and Reduce the Development of Inflammation in the Collagen-Induced Mouse Model of Rheumatoid Arthritis.

Ronan O'Dwyer, Marina Kovaleva, Jiquan Zhang, John Steven, Emma Cummins, Deborah Luxenberg, Alfredo Darmanin-Sheehan, Miguel F Carvalho, Matthew Whitters, Kenneth Saunders and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. VNAR development through antigen immunization of Japanese topeshark (Frontiers in bioengineering and biotechnology · 2023
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

11 authors at 5 institutions in 6 countries.

Ronan O'DwyerImmunocore, Long Wittenham, Oxfordshire OX14 4RY, UK.
Marina KovalevaElasmogen Ltd, Aberdeen AB25 2ZP, UK.ORCID 0000-0001-7614-8261
Jiquan ZhangNovartis Institutes for BioMedical Research (NIBR), Shanghai 201203, China.
John StevenElasmogen Ltd, Aberdeen AB25 2ZP, UK.
Emma CumminsThe Centre for Drug Research and Development (CDRD), Vancouver, BC, Canada V6T 1Z3.
Deborah LuxenbergPfizer, Cambridge Park Drive, Cambridge, MA 02140, USA.
Alfredo Darmanin-SheehanPfizer; Global Biotherapeutics Technologies, Dublin D22, Ireland.ORCID 0000-0001-5280-7090
Miguel F CarvalhoPfizer, Cambridge Park Drive, Cambridge, MA 02140, USA.ORCID 0000-0002-0644-3860
Matthew WhittersPfizer, Cambridge Park Drive, Cambridge, MA 02140, USA.
Kenneth SaundersUCB New Medicines, B1420 Braine-l'Alleud, Belgium.
Caroline J BarelleElasmogen Ltd, Aberdeen AB25 2ZP, UK.ORCID 0000-0003-1872-3373
Pfizer (United States) · USCentre for Drug Research and Development · CAImmunocore (United Kingdom) · GBNovartis (China) · CNUCB Pharma (Belgium) · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphocyte costimulation plays a central role in immunology, inflammation, and immunotherapy. The inducible T cell costimulator (ICOS) is expressed on T cells following peptide: MHC engagement with CD28 costimulation. The interaction of ICOS with its sole ligand, the inducible T cell costimulatory ligand (ICOSL; also known as B7-related protein-1), triggers a number of key activities of T cells including differentiation and cytokine production. Suppression of T cell activation can be achieved by blocking this interaction and has been shown to be an effective means of ameliorating disease in models of autoimmunity. In this study, we isolated specific anti-ICOSL new antigen receptor domains from a synthetic phage display library and demonstrated their ability to block the ICOS/ICOSL interaction and inhibit T cell proliferation. Anti-mouse ICOSL domains, considered here as surrogates for the use of anti-human ICOSL domains in patient therapy, were tested for efficacy in a collagen-induced mouse model of rheumatoid arthritis where they significantly decreased the inflammation of joints and delayed and reduced overall disease progression and severity.

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidCell ProliferationCell Surface Display TechniquesCHO CellsCricetulusDisease Models, AnimalFemaleHumansImmunotherapyInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinInflammationLymphocyte ActivationMiceIcosl protein, mouseIcos protein, mouseInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinReceptors, Antigen, B-CellSingle-Chain Antibodies

Identifiers

PMID30417018
PMCPMC6207862
OpenAlexW2895864000

What OpenQuestion holds

Textmetadata
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.