Targeted Therapies in Psoriatic Arthritis-An Update.

Int J Mol Sci

Centre for Arthritis and Rheumatic Diseases, Dublin Academic Medical Centre, University College Dublin, D04 V1W8 Dublin, Ireland.

Published: March 2023

AI Article Synopsis

  • Psoriatic arthritis (PsA) is a complex inflammatory disease with varying symptoms and has seen advancements in understanding and treatment options over the last decade.
  • Despite these advancements, many patients still do not respond adequately to available therapies, highlighting challenges in personalized treatment strategies due to the disease's heterogeneous nature.
  • Research on the IL-23/IL-17 pathway has opened up new therapeutic possibilities, offering hope for improved outcomes in PsA patients.

Article Abstract

Psoriatic arthritis (PsA) is a systemic inflammatory condition characterised by multiple clinical manifestations. Over the last decade, significant progress has been made in understanding the pathobiology of the disease. An expanded set of targeted therapies have emerged and have shown efficacy in PsA. Nevertheless, there is still a substantial subset of patients who experience no response or only a partial response to currently licensed therapies. The heterogeneous nature of the disease, together with a varying level of severity at presentation and disease activity during follow-up, brings tremendous challenges to devising management strategies. While there are certain pathophysiological similarities between PsA and rheumatoid arthritis (RA), it has become clear that there are discriminating features between these two conditions at the clinical, cellular, and molecular levels. However, there is a degree of overlap in the clinical approach when treating both PsA and RA, given that many biological and targeted therapies have proven efficacy for both pathologies. With an increasing understanding of the relevance of the IL-23/IL-17 axis in PsA, pharmacological agents blocking this pathway have provided promising possibilities for patients with PsA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094037PMC
http://dx.doi.org/10.3390/ijms24076384DOI Listing

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