Chan Tom C, Hawkes Jason E, Krueger James G
Laboratory for Investigative Dermatology, The Rockefeller University, New York, NY, USA.
The Milstein Research Program, Laboratory Head, Investigative Dermatology, The Rockefeller University, 1230 York Avenue, Box 178, New York, NY 10065, USA.
Ther Adv Chronic Dis. 2018 May;9(5):111-119. doi: 10.1177/2040622318759282. Epub 2018 Mar 19.
Plaque psoriasis is one of the most common autoimmune skin diseases and is characterized by erythematous, scaly plaques. Many highly effective, targeted therapies have been developed as a result of an improved understanding of the pathogenesis of psoriasis. Using agents that target the central interleukin (IL)-23/IL-17 immune axis, this once difficult-to-treat disease is now among the most effectively treated autoimmune diseases with major clinical improvements possible in around 90% of patients. In this article, we outline the immune mechanisms responsible for the development of psoriasis and provide an overview of the novel IL-23 antagonists being used to manage this chronic skin disease.
斑块状银屑病是最常见的自身免疫性皮肤病之一,其特征为红斑鳞屑性斑块。由于对银屑病发病机制的认识有所提高,现已开发出许多高效的靶向疗法。使用靶向核心白细胞介素(IL)-23/IL-17免疫轴的药物,这种曾经难以治疗的疾病如今已成为最易有效治疗的自身免疫性疾病之一,约90%的患者可能实现显著的临床改善。在本文中,我们概述了银屑病发病的免疫机制,并对用于治疗这种慢性皮肤病的新型IL-23拮抗剂进行了综述。