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Targeted Therapies in Psoriatic Arthritis-An Update
被引:10
作者:
Sundanum, Sonia
[1
]
Orr, Carl
[1
]
Veale, Douglas
[1
]
机构:
[1] Univ Coll Dublin, Ctr Arthrit & Rheumat Dis, Dublin Acad Med Ctr, Dublin D04 V1W8, Ireland
关键词:
psoriatic arthritis;
targeted therapy;
IL-17;
pathway;
TUMOR-NECROSIS-FACTOR;
INTERLEUKIN-12/23;
MONOCLONAL-ANTIBODY;
DOUBLE-BLIND;
ANKYLOSING-SPONDYLITIS;
PHASE-III;
RHEUMATOID-ARTHRITIS;
INADEQUATE RESPONSE;
PLAQUE PSORIASIS;
DISEASE-ACTIVITY;
EARLY SYNOVITIS;
D O I:
10.3390/ijms24076384
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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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页数:22
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