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Novel therapies in axial spondyloarthritis
Mohamad Bittar1, Philip Mease2
1The University of Tennessee Health Science Center, Division of Connective Tissue Disease (Rheumatology), 956 Court Avenue, Coleman Building, Suite G326, Memphis, TN 38163, USA.
Abstract:
Over the past two decades, advancements in understanding the pathogenesis of axial spondyloarthritis have led to discoveries of new therapeutic targets, particularly the interleukin-17, tumor necrosis factor axis, and Janus kinase-signal transducer and activator of transcription pathway. While many of the available agents have proven to be efficacious and safe for the treatment of axial spondyloarthritis, a remarkable percentage of patients either fail or cannot tolerate these medications. This has prompted researchers to look for new targets that would maximize efficacy and minimize toxicity. In this article, we review novel agents that were recently approved, in trials, and possible future targets or mechanisms. We also discuss their role as it pertains to the prevention of radiographic progression and the management of extra-musculoskeletal manifestations.
Insights
New treatments for axial spondyloarthritis (axSpA) are emerging due to limitations of current therapies. This review covers novel agents, future targets, and their impact on disease progression and extra-musculoskeletal symptoms.
Area of Science:
- Rheumatology and Immunology
- Inflammatory Disease Pathogenesis
Background:
- Advances in understanding axial spondyloarthritis (axSpA) pathogenesis have identified key therapeutic targets.
- Current treatments targeting interleukin-17, tumor necrosis factor (TNF), and Janus kinase (JAK) pathways show efficacy but have limitations.
- A significant patient subset experiences treatment failure or intolerance with existing axSpA therapies.
Purpose of the Study:
- To review recently approved and investigational agents for axSpA.
- To explore novel therapeutic targets and mechanisms for axSpA management.
- To discuss the role of new therapies in preventing radiographic progression and managing extra-musculoskeletal manifestations.
Main Methods:
- Literature review of recent advancements in axSpA therapeutics.
- Analysis of approved, clinical trial, and preclinical novel agents.
- Discussion of therapeutic strategies for axSpA and its complications.
Main Results:
- Several novel agents targeting distinct pathways are in development or recently approved.
- Future therapeutic strategies aim to improve efficacy and reduce toxicity in axSpA.
- Emerging treatments show potential in addressing radiographic progression and extra-musculoskeletal symptoms.
Conclusions:
- The landscape of axSpA treatment is evolving with new therapeutic options.
- Addressing unmet needs requires continued research into novel targets and mechanisms.
- Optimizing treatment strategies is crucial for comprehensive management of axSpA patients.
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