Dermatologic Clinics, volume 42, issue 3, pages 339-355
Biologics for Psoriasis
Mitchel Wride
1
,
Gloria F. Chen
1
,
Sarah L Spaulding
1
,
E. Tkachenko
1
,
Jeffrey M. Cohen
1
Publication type: Journal Article
Publication date: 2024-07-01
Journal:
Dermatologic Clinics
scimago Q1
SJR: 0.792
CiteScore: 4.5
Impact factor: 2.2
ISSN: 07338635, 15580520
Dermatology
Abstract
Biologic therapies targeting tumor necrosis factor alpha (TNF-α) (infliximab, adalimumab, certolizumab, etanercept), the p40 subunit shared by IL-12 and IL-23 (ustekinumab), the p19 subunit of IL-23 (guselkumab, tildrakizumab, risankizumab), IL-17A (secukinumab, ixekizumab), IL-17-RA (brodalumab) and both IL-17A and IL-17F (bimekizumab) have revolutionized the treatment of psoriasis. In both the short and long term, risankizumab had highest Psoriasis Area and Severity Index 90 scores compared to other oral and injectable biologics. IL-23 inhibitors had lowest rates of short-term and long-term adverse events and most favorable long-term risk-benefit profile compared to IL-17, IL-12/23, and TNF-α inhibitors.
Found
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