Cited by 58Rheumatoid Arthritis Research and TherapiesNatural Compounds in Disease TreatmentAutoimmune and Inflammatory Disorders Research

Investigational IRAK-4 inhibitors for the treatment of rheumatoid arthritis

Wiese, Michael D., Manning-Bennett, Arkady T., Abuhelwa, Ahmad Y.·2020·Expert Opinion on Investigational Drugs

Abstract

INTRODUCTION: Rheumatoid arthritis (RA) is a chronic inflammatory auto-immune disease that can lead to permanent disability and deformity. Despite current treatment modalities, many patients are still unable to reach remission. Interleukin-1 receptor-associated kinase 4 (IRAK-4) inhibitors are novel agents designed to suppress immune signaling pathways involved in inflammation and joint destruction in RA. Four IRAK-4 inhibitors have entered clinical trials. AREAS COVERED: This review summarizes the current stage of development of IRAK-4 inhibitors in clinical trials, detailing their chemistry, pharmacokinetics, and therapeutic potential in the treatment of RA. PubMed, Embase and restricted Google searches were conducted using the term 'IRAK-4', and publicly accessible clinical trial databases were reviewed. EXPERT OPINION: IRAK-4 inhibitors are an exciting therapeutic option in RA management because unlike other targeted disease-modifying agents, they target the innate immune system. The role of IRAK-4 as a key component of Toll/Interleukin-1 receptor signaling and its potential for a low rate of infectious complications is particularly exciting and this may facilitate their use in combination treatment. A key aspect of upcoming clinical trials will be the identification of biomarkers predictive of treatment efficacy, which will help to define if and how they will be used in the clinic.

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Crossref · 10.1080/13543784.2020.1752660

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  • The role of IRAK4 in inflammatory conditions, as well as in B cell lymphomas, is well established, and several inhibitors are currently in clinical trials in autoimmune indications.

    “but the role of IRAK4 in inflammatory conditions, as well as in B cell lymphomas, is well established, and several inhibitors are currently in clinical trials in autoimmune indications165,171.”

    From PROTAC targeted protein degraders: the past is prologue (2022) · cites this paper as [171]

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References 66 · Cited by 58

Authors
Wiese, M. D., Manning-Bennett, A. T., & Abuhelwa, A. Y.
Affiliations
  • University of South Australia (AU)
  • Clinical and Health Sciences, University of South Australia, Adelaide, Australia
Corresponding author
Wiese, Michael D.
Venue
Expert Opinion on Investigational Drugs
Published
2020-04-17
Volume
29
Issue
5
Pages
475-482
ISSN
  • 1354-3784 (ISSN-L)
  • 1744-7658
OpenAlex
W3014980743
Cited by
58
References
66
Citations by year
2026: 4 · 2025: 7 · 2024: 10 · 2023: 9 · 2022: 14 · 2021: 10 · 2020: 3
FWCI
1.44
Type
journal article
Language
en
Open access
closed
Locations
  • Expert Opinion on Investigational Drugs (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
  • Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
  • Health Sciences › Medicine › Hematology › Autoimmune and Inflammatory Disorders Research
Keywords
rheumatoid arthritis, IRAK4, Toll-like receptor signaling, innate immunity, disease-modifying antirheumatic drugs, pharmacokinetics, clinical trials, biomarkers, infectious complications, combination therapy
MeSH terms
Drug Development, Animals, Arthritis, Rheumatoid, Humans, Immunity, Innate, Inflammation, Signal Transduction, Antirheumatic Agents, Interleukin-1 Receptor-Associated Kinases

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