IL-17 targeted therapies for psoriasis

被引:136
|
作者
Chiricozzi, Andrea [1 ]
Krueger, James G. [1 ,2 ,3 ]
机构
[1] Rockefeller Univ, Lab Invest Dermatol, New York, NY 10065 USA
[2] Rockefeller Univ, Milstein Med Res Program, New York, NY 10065 USA
[3] Rockefeller Univ, New York, NY 10065 USA
关键词
anti-IL-17; agents; brodalumab; IL-17; ixekizumab; psoriasis; secukinumab; T-CELL POPULATION; DENDRITIC CELLS; AUTOIMMUNE INFLAMMATION; HUMAN SKIN; EPIDERMAL HYPERPLASIA; MONOCLONAL-ANTIBODY; PLAQUE PSORIASIS; CYTOKINE FAMILY; INTERLEUKIN; 22; HELPER TYPE-1;
D O I
10.1517/13543784.2013.806483
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Psoriasis is a chronic, disabling, inflammatory skin disease whose pathogenesis still remains to be fully elucidated. Genetic and environmental factors induce an immune response mediated by several cytokines and chemokines, including IL-17A. Areas covered: Emerging evidence now suggests that IL-17A is central in the pathogenesis of psoriasis. Three agents neutralizing IL-17 (i.e., secukinumab and ixekizumab) or antagonizing its receptor (i.e., brodalumab) are in development and are being studied in Phase III clinical trials to evaluate their overall efficacy and safety. However, Phase II results of IL-17 blockade with each of these agents has shown a marked improvement of disease severity, thus confirming the pathogenic relevance of IL-17 in mediating crucial inflammatory circuits in psoriasis. Expert opinion: Anti-IL-17 agents are likely to become important future therapeutics in this disease and the may potentially impact on cardiovascular diseases, arthritis and other comorbidities associated with psoriasis.
引用
收藏
页码:993 / 1005
页数:13
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