Highly Effective New Treatments for Psoriasis Target the IL-23/Type 17 T Cell Autoimmune Axis

被引:137
作者
Kim, Jaehwan [1 ]
Krueger, James G. [1 ]
机构
[1] Rockefeller Univ, Lab Invest Dermatol, New York, NY 10065 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 68 | 2017年 / 68卷
关键词
psoriasis vulgaris; IL-17; antagonists; IL-23; TNF antagonists; pathogenesis of psoriasis; biologic drugs; cytokines; polar T cell subsets; PLACEBO-CONTROLLED TRIAL; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; INNATE LYMPHOID-CELLS; LONG-TERM EFFICACY; PHASE-III TRIAL; DENDRITIC CELLS; DOUBLE-BLIND; PLAQUE PSORIASIS; ANTIMICROBIAL PEPTIDE; HUMAN SKIN;
D O I
10.1146/annurev-med-042915-103905
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Psoriasis vulgaris, affecting the skin, is one of the most common organ-specific autoimmune diseases in humans. Until recently, psoriasis was treated by agents or approaches discovered largely through serendipity. Many of the available drugs were inherently quite toxic when used as continuous treatment for many years in this chronic disease. However, an increasing understanding of disease-specific immune pathways has spurred development of pathway-targeted therapeutics during the past decade. Psoriasis is now the most effectively treated human autoimmune disease, with high-level clinical improvements possible in similar to 90% of patients using a new generation of drugs that selectively target the IL-23/Type 17 T cell axis. Thus, psoriasis is a model for the success of a translational-medicine approach based on cellular and molecular dissection of disease pathogenesis in humans.
引用
收藏
页码:255 / 269
页数:15
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