Abstract | BACKGROUND:
Psoriasis is a chronic, immune-mediated inflammatory skin disorder of unknown etiology. Interleukin (IL)-17a, a key product of the recently identified Th17 cell subset, has been found to play a critical role in the immunopathogenesis of psoriasis. IL-17 antagonists are a new class of biological agent currently in development for psoriasis that selectively inhibit IL-17a activity. OBJECTIVE: CONCLUSION: Patients treated with IL-17 antagonists achieved marked reduction in psoriasis disease severity as demonstrated by the Psoriasis Area and Severity Index (PASI) 75 response rates. A sizable proportion of patients treated with brodalumab and ixekizumab achieved unprecedented clinical clearance of their psoriasis (PASI > 90). These encouraging results demonstrate the efficacy of these agents and validate the pro-inflammatory role of IL-17 in the pathophysiology of psoriasis.
|
Authors | Shivani Felicia Chandrakumar, Jensen Yeung |
Journal | Journal of cutaneous medicine and surgery
(J Cutan Med Surg)
2015 Mar-Apr
Vol. 19
Issue 2
Pg. 109-14
ISSN: 1203-4754 [Print] United States |
PMID | 25775627
(Publication Type: Journal Article, Review)
|
Copyright | © 2014 Canadian Dermatology Association. |
Chemical References |
- Biological Factors
- Interleukin-17
|
Topics |
- Biological Factors
(therapeutic use)
- Humans
- Interleukin-17
(antagonists & inhibitors)
- Psoriasis
(drug therapy, pathology)
- Skin
(pathology)
- Treatment Outcome
|