دورية أكاديمية

New Treatment Addressing the Pathogenesis of Psoriasis

التفاصيل البيبلوغرافية
العنوان: New Treatment Addressing the Pathogenesis of Psoriasis
المؤلفون: Michio Tokuyama, Tomotaka Mabuchi
المصدر: International Journal of Molecular Sciences, Vol 21, Iss 20, p 7488 (2020)
بيانات النشر: MDPI AG, 2020.
سنة النشر: 2020
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: psoriasis, new treatment, pathogenesis, dendritic cells, Janus kinase inhibitor, sphingosine 1-phosphate receptor 1, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: Psoriasis is an immune cell-mediated inflammatory skin disease. The interleukin (IL)23/IL17 axis plays an important role in the development of psoriasis. The effectiveness of biologic treatments such as tumor necrosis factor (TNF)α inhibitors (infliximab, adalimumab, certolizumab pegol), IL23 inhibitors (ustekinumab, guselkumab, tildrakizumab, risankizumab), and IL17 inhibitors (secukinumab, ixekizumab, brodalumab) have verified these findings. Immune-related cells such as dendritic cells (DCs) and macrophages, in addition to Toll-like receptors and cytokines such as interferon (IFN)α, TNFα, IFNɤ, IL12, IL22, IL23, and IL17, are related to the pathogenesis of psoriasis. Here, we first review new insights regarding the pathogenesis of psoriasis, as it relates to DCs, Langerhans cells, macrophages, the signal transducer and activator of transcription 3 pathway, and aryl hydrocarbon receptor in cutaneous vascular endothelial cells. Based on these findings, we summarize currently available oral treatments and biologics. Furthermore, we describe a new treatment option including Janus kinase inhibitor, tyrosine kinase 2 inhibitor, modulator of sphingosine 1-phosphate receptor 1, and Rho-associated kinase 2 inhibitor.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 21207488
1422-0067
1661-6596
Relation: https://www.mdpi.com/1422-0067/21/20/7488; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms21207488
URL الوصول: https://doaj.org/article/94cdf9c402da400eb5ed745fc566ea94
رقم الأكسشن: edsdoj.94cdf9c402da400eb5ed745fc566ea94
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21207488
14220067
16616596
DOI:10.3390/ijms21207488