López-Ferrer A, Laiz A, Puig L
a Department of Dermatology , Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona , Barcelona , Spain.
b Unit of Rheumatology, Hospital de la Santa Creu i Sant Pau , Universitat Autònoma de Barcelona , Barcelona , Spain.
Expert Opin Drug Saf. 2017 Jun;16(6):733-742. doi: 10.1080/14740338.2017.1323864. Epub 2017 May 9.
The cytokines interleukin (IL)-12 and IL-23 have been involved in the pathogenesis of psoriasis and psoriatic arthritis. Ustekinumab is a fully human monoclonal antibody targeting the p40 subunit shared by IL-12 and IL-23. Ustekinumab prevents the interaction of IL-12 and IL-23 binding to their receptors, blocking the T1 and T17 inflammatory pathways. Ustekinumab has been evaluated for the treatment of various chronic immune mediated diseases including psoriasis and psoriatic arthritis (PsA). Most of the data regarding the safety of ustekinumab come from the experience treating patients with psoriasis, but clinical trials have demonstrated its efficacy and safety in the treatment of both diseases. The most common adverse events observed during the clinical trials are mild in intensity, and include respiratory tract infections, nasopharyngitis, headache and injection site reactions. Throughout long-term ustekinumab treatment, serious infections or major cardiovascular adverse events occurred rarely. Areas covered: In this review we report the safety data that come from phase II and phase III clinical trials that assay the efficacy and safety of ustekinumab in PsA, including recently published data corresponding to long-term studies. Relevant references were obtained through a literature search in MEDLINE/Pubmed (search strategy: ustekinumab AND psoriatic arthritis) for articles published until November 2016, complemented by a manual search. Expert opinion: In clinical practice, ustekinumab is generally a well-tolerated treatment, and the safety profile in psoriatic arthritis is similar to that reported in plaque psoriasis.
细胞因子白细胞介素(IL)-12和IL-23参与了银屑病和银屑病关节炎的发病机制。优特克单抗是一种全人源单克隆抗体,靶向IL-12和IL-23共有的p40亚基。优特克单抗可防止IL-12和IL-23与其受体结合的相互作用,阻断T1和T17炎症途径。优特克单抗已被评估用于治疗包括银屑病和银屑病关节炎(PsA)在内的各种慢性免疫介导疾病。关于优特克单抗安全性的大多数数据来自治疗银屑病患者的经验,但临床试验已证明其在治疗这两种疾病方面的有效性和安全性。临床试验期间观察到的最常见不良事件强度较轻,包括呼吸道感染、鼻咽炎、头痛和注射部位反应。在优特克单抗的长期治疗过程中,严重感染或重大心血管不良事件很少发生。涵盖领域:在本综述中,我们报告了来自II期和III期临床试验的安全性数据,这些试验测定了优特克单抗在PsA中的有效性和安全性,包括最近发表的长期研究数据。通过在MEDLINE/Pubmed中进行文献检索(检索策略:优特克单抗AND银屑病关节炎)获取截至2016年11月发表的文章的相关参考文献,并辅以人工检索。专家意见:在临床实践中,优特克单抗通常是一种耐受性良好的治疗方法,银屑病关节炎中的安全性概况与斑块状银屑病中报告的相似。