作者: Laura J. Savage , Miriam Wittmann , Dennis McGonagle , Philip S. Helliwell
DOI: 10.1007/S40744-015-0010-2
关键词: Rheumatology 、 Psoriasis 、 Psoriatic arthritis 、 Disease 、 Internal medicine 、 Ustekinumab 、 Immunology 、 Interleukin 、 Inflammation 、 Pathogenesis 、 Medicine
摘要: Biologics have revolutionized the therapy of psoriatic disease spectrum. These new classes drugs also allow deeper insight into pathogenesis and highlight existence distinct "molecular" subgroups as evidenced by spectrum clinical response seen. Molecules associated with both interleukin (IL)-17 interferon (IFN)γ pathways important functions in inflammation, are targeted acting on p40 subunit shared IL-12 IL-23. family members upstream characterized production IFNγ IL-17 related molecules, including IL-17, IL-22, CCL20. We here summarize mode action studies inhibitor ustekinumab focus psoriasis arthritis.