Evidence map›Paper›PMID 24671001›Full record

ArticlemAbs

A novel human anti-interleukin-1β neutralizing monoclonal antibody showing in vivo efficacy.

Angeline X H Goh, Sebastien Bertin-Maghit, Siok Ping Yeo, Adrian W S Ho, Heidi Derks, Alessandra Mortellaro, Cheng-I Wang

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Immunological Prognostic Factors in Multiple Myeloma.International journal of molecular sciences · 2021
    Review
  10. Canakinumab as treatment for COVID-19-related pneumonia: A prospective case-control study.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Observational
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Imaging PD-L1 Expression with ImmunoPET.Bioconjugate chemistry · 2018
    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 3 institutions in 2 countries.

Angeline X H GohSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Sebastien Bertin-MaghitSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Siok Ping YeoSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Adrian W S HoSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Heidi DerksSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Alessandra MortellaroSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Cheng-I WangSingapore Immunology Network; Agency for Science; Technology and Research (A*STAR); Singapore.
Agency for Science, Technology and Research · SGStar Technology and Research (United States) · USSingapore Immunology Network · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pro-inflammatory cytokine interleukin (IL)-1β is a clinical target in many conditions involving dysregulation of the immune system; therapeutics that block IL-1β have been approved to treat diseases such as rheumatoid arthritis (RA), neonatal onset multisystem inflammatory diseases, cryopyrin-associated periodic syndromes, active systemic juvenile idiopathic arthritis. Here, we report the generation and engineering of a new fully human antibody that binds tightly to IL-1β with a neutralization potency more than 10 times higher than that of the marketed antibody canakinumab. After affinity maturation, the derived antibody shows a>30-fold increased affinity to human IL-1β compared with its parent antibody. This anti-human IL-1β IgG also cross-reacts with mouse and monkey IL-1β, hence facilitating preclinical development. In a number of mouse models, this antibody efficiently reduced or abolished signs of disease associated with IL-1β pathology. Due to its high affinity for the cytokine and its potency both in vitro and in vivo, we propose that this novel fully human anti-IL-1β monoclonal antibody is a promising therapeutic candidate and a potential alternative to the current therapeutic arsenal.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingAntibody AffinityArthritis, ExperimentalCross ReactionsDisease Models, AnimalEpitopesFemaleHumansImmunoglobulin GInflammationInterleukin-1betaMacaca mulattaMiceAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingcanakinumabEpitopesImmunoglobulin GInterleukin-1betaPeptide Libraryanimal modelsantibodydrug discoveryimmunotherapyinterleukin 1

Identifiers

PMID24671001
PMCPMC4011920
OpenAlexW2131592022

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.