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Existing and Emerging Targeted Therapies in Juvenile Psoriatic Arthritis: Challenges and Unmet Needs
Sarrah Lokhandwala1, Jaiden Townsend2, Coziana Ciurtin3
1Department of Biomedical Sciences, University College London, London, UK.
Insights
Juvenile psoriatic arthritis (JPsA) treatment faces challenges in harmonizing recommendations. Emerging therapies show promise, but further research is needed for optimal JPsA management and patient outcomes.
Area of Science:
- Rheumatology
- Pediatric Rheumatology
- Immunology
Background:
- Juvenile psoriatic arthritis (JPsA) is a complex chronic inflammatory condition in children and young people.
- Heterogeneity in JPsA necessitates tailored therapeutic approaches based on distinct clinical phenotypes.
Purpose of the Study:
- To review challenges in harmonizing JPsA treatment recommendations across different age groups and clinical presentations.
- To explore the evolving therapeutic landscape, including recent clinical trials and ongoing research in JPsA and adult psoriatic arthritis.
- To identify unmet needs and barriers hindering translational research in JPsA.
Main Methods:
- Literature review focusing on JPsA classification, management strategies, and therapeutic advancements.
- Analysis of completed and ongoing clinical trials for novel agents targeting inflammatory pathways (e.g., IL-17, IL-23, JAK).
- Exploration of head-to-head trial data comparing different biologic agents.
Main Results:
- Novel therapies including monoclonal antibodies (anti-IL-17, anti-IL-12/23, anti-IL-23) and small molecules (JAK, TK, PDE4 inhibitors) are under development.
- Many new agents, initially tested in adult psoriatic arthritis, show promising efficacy and safety profiles, advancing to Phase III or gaining approval.
- Head-to-head trials provide comparative data for biologic therapies like TNF-α blockade versus IL-17 and IL-23 inhibitors.
Conclusions:
- Emerging JPsA therapies demonstrate potential for improved efficacy and tolerability, mirroring advancements in adult psoriatic arthritis treatment.
- Further translational research is crucial to understand age-specific treatment efficacy and manage refractory JPsA for better long-term patient outcomes.
- Addressing unmet needs and research barriers will facilitate the translation of novel therapies for JPsA patients.
Abstract:
Juvenile psoriatic arthritis (JPsA) is a heterogeneous type of non-systemic chronic inflammatory arthritis affecting children and young people. This review focuses on highlighting challenges in harmonising recommendations for the use of available therapies in JPsA, according to its distinct clinical phenotypes, and explores the similarities and differences between the disease classification and management across age. We further explore the emerging therapeutic landscape, summarising the recently completed clinical trials in JPsA, and ongoing studies in both JPsA and adults with psoriatic arthritis, highlighting unmet needs and barriers for translational research in JPsA. The novel therapeutic agents in clinical development in JPsA range from monoclonal antibodies targeting interleukin (IL)-17, IL-12/23 and IL-23 blockades to synthetic small molecules targeting Janus kinase and tyrosine kinase and phosphodiesterase-4 inhibition. In addition, there are head-to-head clinical trials comparing tumour necrosis factor-α blockade with both IL-17 and IL-23 inhibition. Most of these new therapies have been tested in adults with psoriatic arthritis and have advanced to the phase III stage of drug development or received license for use, suggesting promising signals for efficacy and potentially acceptable safety and tolerability for JPsA. Further translational research in JPsA is required to improve our understanding of the impact of age at onset on treatment efficacy, as well as to provide opportunities for better management of refractory disease and improved long-term outcomes in JPsA, for ultimate patient benefit.
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