Evidence map›Paper›PMID 32700979›Full record

ReviewExpert opinion on investigational drugs2020

Type I interferon antagonists in clinical development for lupus.

Jacqueline L Paredes, Timothy B Niewold

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Inhibiting the P2YJACC. Basic to translational science · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Type I Interferons in Autoimmunity.The Journal of investigative dermatology · 2022
    Review
  13. Article
  14. Pharmaceuticals (Basel, Switzerland) · 2021
    Article
  15. COVID-19 in patients with systemic lupus erythematosus: lessons learned from the inflammatory disease.Translational research : the journal of laboratory and clinical medicine · 2021
    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

2 authors at 2 institutions in 1 country.

Jacqueline L ParedesColton Center for Autoimmunity, New York University School of Medicine , New York, NY, USA.
Timothy B NiewoldColton Center for Autoimmunity, New York University School of Medicine , New York, NY, USA.
Autoimmune Technologies (United States) · USNew York University · US

Funding

Interferon Regulatory Factor 5 in Human Lupus PathogenesisR01AR065964 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NIEWOLD, TIMOTHY B · 2015 to 2018
$2.0M
Interferon Alpha as a Tool for Gene Discovery in Human LupusR01AR060861 · NIAMS · UNIVERSITY OF CHICAGO · PI NIEWOLD, TIMOTHY B · 2011 to 2015
$1.8M
Novel Anti-Proteinuric Strategies Targeting PodocytesR01DK107984 · NIDDK · RUSH UNIVERSITY MEDICAL CENTER · PI GUPTA, VINEET, REISER, JOCHEN · 2016 to 2019
$1.8M
NIAMS NIH HHS R01 AR060861NIAMS NIH HHS R01 AR065964NIDDK NIH HHS R01 DK107984
6 · The paper itself

Abstract

introductionSystemic lupus erythematosus (SLE) is a severe chronic and incurable autoimmune disease. Treatment includes glucocorticoids and immunosuppressants which typically result in partial responses, and hence there is a great need for new therapies. The type I interferon (IFN) pathway is activated in more than 50% of SLE patients, and it is strongly implicated as a pathogenic factor in SLE. AREAS COVERED: We searched the literature using 'SLE and interferon antagonists' as search terms. This identified a number of therapeutics that have entered clinical development targeting type I IFN in SLE. These include monoclonal antibodies against type I IFN cytokines and a kinoid vaccination strategy to induce anti-IFN antibodies. EXPERT OPINION: Type I IFN antagonists have had some success, but many molecules have not progressed to phase III. These varied results are likely attributed to the multiple concurrent cytokine abnormalities present in SLE, the imprecise nature of the IFN signature as a readout for type I IFN and difficulties with clinical trials such as background medication use and diffuse composite disease activity measures. Despite these challenges, it seems likely that a type I IFN antagonist will come to clinical utility for SLE given the large unmet need and the recent phase III success with anifrolumab.

Indexed as

Drug DevelopmentAnimalsAntibodies, MonoclonalCytokinesHumansInterferon Type ILupus Erythematosus, SystemicAntibodies, MonoclonalCytokinesInterferon Type Iautoimmune diseaseclinical trialsIFN pathwayinterferonLupussystemic lupus erythematosustype I IFN antagoniststype I interferon pathway

Identifiers

PMID32700979
PMCPMC7924012
OpenAlexW3044340667

What OpenQuestion holds

Textmetadata
LicenceTDM
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.