Plaque-type psoriasis inhibitors

被引:8
作者
Shobeiri, Saeideh Sadat [1 ]
Khorrami, Motahareh [1 ]
Sankian, Mojtaba [1 ]
机构
[1] Mashhad Univ Med Sci, Immunol Res Ctr, Sch Med, Mashhad, Razavi Khorasan, Iran
关键词
Psoriasis; Inhibitor; Treatment; Biologics; Small molecule; Aptamer; JANUS KINASE INHIBITOR; PHASE-III; IMPROVES PSORIASIS; CONTROLLED-TRIAL; DOUBLE-BLIND; DNA APTAMER; MODERATE; EFFICACY; SAFETY; PATHOGENESIS;
D O I
10.1016/j.intimp.2021.108326
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Psoriasis is a common inflammatory skin disorder, which is mediated by the immune system and affects 1-4% of the world's population. Psoriasis is caused by a complex interaction between the immune system, autoantigens, psoriasis-associated genetic factors, and various environmental factors. As a chronic disease requiring long-term treatment, psoriasis is associated with follow-up costs and an economic burden on the patients, their families, and healthcare systems. The current treatments for moderate-to-severe plaque psoriasis include topical therapy, phototherapy, and systemic drugs consisting of biological/non-biological drugs. Within the past two decades, recent biological therapies for psoriasis have rapidly advanced. Moreover, new bispecific agents have the potential for better disease control, while small molecule drugs offer a future alternative to biological drugs and the more cost-effective, long-term treatment of the disease. The present study aimed to review updated data regarding the inhibitors used to improve plaque psoriasis that contain biologics, bispecific agents, small molecules, and aptamers (either approved or in the research phase).
引用
收藏
页数:14
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