Evidence map›Paper›PMID 26540618›Full record

ArticleClinical and experimental immunology2016

Clinical efficacy of a new CD28-targeting antagonist of T cell co-stimulation in a non-human primate model of collagen-induced arthritis.

M P M Vierboom, E Breedveld, Y S Kap, C Mary, N Poirier, B A 't Hart, B Vanhove

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2016. 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
2.1field-weighted citation impact, top 13% 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, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Predictors of Subcutaneous Injection Site Reactions to Sustained-Release Buprenorphine in Rhesus Macaques (Journal of the American Association for Laboratory Animal Science : JAALAS · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. CD28 BlockadeFrontiers in immunology · 2017
    Article
  15. Review
  16. Article
  17. First report of expansion of CD4Hematology, transfusion and cell therapy
    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

7 authors at 2 institutions in 2 countries.

M P M VierboomDepartment of Immunobiology, Biomedical Primate Research Centre, Rijswijk, the Netherlands.
E BreedveldDepartment of Immunobiology, Biomedical Primate Research Centre, Rijswijk, the Netherlands.
Y S KapDepartment of Immunobiology, Biomedical Primate Research Centre, Rijswijk, the Netherlands.
C MaryInstitut National De La Santé Et De La Recherche Médicale, Université De Nantes, Effimune SA, Nantes, France.
N PoirierInstitut National De La Santé Et De La Recherche Médicale, Université De Nantes, Effimune SA, Nantes, France.
B A 't HartDepartment of Immunobiology, Biomedical Primate Research Centre, Rijswijk, the Netherlands.
B VanhoveInstitut National De La Santé Et De La Recherche Médicale, Université De Nantes, Effimune SA, Nantes, France.
Biomedical Primate Research Centre · NLNantes Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells have a central pathogenic role in the aetiopathogenesis of rheumatoid arthritis (RA), and are therefore a favoured target of immunotherapy aiming at physical or functional elimination. Here we report an efficacy test of FR104, a new co-stimulation inhibitor directly targeting CD28 on T cells, in a translationally relevant model, the rhesus monkey model of collagen-induced arthritis (CIA). As a relevant comparator we used abatacept [cytotoxic T lymphocyte antigen immunoglobulin (CTLA Ig)], an antagonist of CTLA-4 binding to CD80/86 clinically approved for treatment of RA. Treatment with either compound was started at the day of CIA induction. Although FR104 previously demonstrated a higher control of T cell responses in vitro than abatacept, both compounds were equally potent in the suppression of CIA symptoms and biomarkers, such as the production of C-reactive protein (CRP) and interleukin (IL)-6 and anti-collagen type II (CII) serum antibody (IgM/IgG). However, in contrast to abatacept, FR104 showed effective suppression of CII-induced peripheral blood mononuclear cell (PBMC) proliferation. The current study demonstrates a strong potential of the new selective CD28 antagonist FR104 for treatment of RA.

Indexed as

AbataceptAnimalsAntirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidAutoimmunityCD28 AntigensCollagenC-Reactive ProteinDrug Administration ScheduleFemaleHumansInterleukin-6Lymphocyte ActivationMacaca mulattaMaleAbataceptAntirheumatic AgentsCD28 AntigensCollagenC-Reactive ProteinInterleukin-6CD28CIAco-stimulation blockaderhesus monkeyT cell

Identifiers

PMID26540618
PMCPMC4750591
OpenAlexW2157731456

What OpenQuestion holds

Textmetadata
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.