Kellen Roselyn, Silverberg Nanette B, Lebwohl Mark
Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Dermatology, Mount Sinai St Luke's-Roosevelt Hospital, New York, NY, USA.
Pediatric Health Med Ther. 2016 Sep 19;7:109-120. doi: 10.2147/PHMT.S75836. eCollection 2016.
The biologic agent ustekinumab is a human monoclonal antibody that binds to the p40 subunit shared by interleukins (ILs) 12 and 23. The antibody is able to prevent binding of cytokines to the IL-12Rβ1 cell surface receptor and therefore may prevent IL-23 driven activation of the IL-23/Th 17 axis of inflammation. The anti-inflammatory activity has been beneficial in adult psoriasis. Ustekinumab has been approved in the United States for the treatment of adults with psoriasis and psoriatic arthritis. Approval in children and adolescents has not been granted by the US Food and Drug Administration. Subcutaneous injections of ustekinumab are administered at baseline, week 4 and every 12 weeks thereafter, a regimen that is particularly appealing to young patients who do not like more frequent injections at home. The product is attractive because, although it works through an immune system mechanism, the selective activity is such that the drug has not been associated with many of the side effects attributed to other immunosuppressive medications. Case reports of ustekinumab for pediatric psoriasis have shown promising results, and the recent Phase III CADMUS trial tested the agent in adolescents aged 12-17 years with psoriasis, using standard dose 0.75 mg/kg (≤60 kg), 45 mg (>60-≤100 kg), and 90 mg (>100 kg) or half-standard dosing 0.375 mg/kg (≤60 kg), 22.5 mg (>60-≤100 kg), and 45 mg (>100 kg) with a loading dosage at week 0 and week 4. Psoriasis area and severity index-75 was achieved in more than three-quarters of patients in full and half dosing by 12 weeks, and psoriasis area and severity index-90 in 54.1% and 61.1% of half and full dosage by 12 weeks, respectively. Ustekinumab was generally well tolerated in adolescents, with some patients developing antibodies, and nasopharyngitis being the major adverse event. Ustekinumab is a promising agent in adolescent psoriasis that appears to be well tolerated. The best monitoring plan and usage in younger patients still remain to be defined.
生物制剂优特克单抗是一种人源单克隆抗体,可与白细胞介素(IL)-12和IL-23共有的p40亚基结合。该抗体能够阻止细胞因子与IL-12Rβ1细胞表面受体结合,因此可能阻止IL-23驱动的炎症IL-23/Th17轴的激活。这种抗炎活性对成人银屑病有益。优特克单抗已在美国获批用于治疗成人银屑病和银屑病关节炎。美国食品药品监督管理局尚未批准其用于儿童和青少年。优特克单抗皮下注射在基线时、第4周以及此后每12周进行一次,这种给药方案对不喜欢在家更频繁注射的年轻患者特别有吸引力。该产品很有吸引力,因为尽管它通过免疫系统机制起作用,但选择性活性使得该药物与许多其他免疫抑制药物的副作用无关。关于优特克单抗治疗儿童银屑病的病例报告显示了有希望的结果,最近的III期CADMUS试验在12至17岁的银屑病青少年中测试了该药物,使用标准剂量0.75mg/kg(≤60kg)、45mg(>60至≤100kg)和90mg(>100kg)或半标准剂量0.375mg/kg(≤60kg)、22.5mg(>60至≤100kg)和45mg(>100kg),在第0周和第4周有负荷剂量。到12周时,超过四分之三接受全剂量和半剂量治疗的患者达到银屑病面积和严重程度指数-75,接受半剂量和全剂量治疗的患者分别有54.1%和61.1%在12周时达到银屑病面积和严重程度指数-90。优特克单抗在青少年中总体耐受性良好,一些患者产生了抗体,鼻咽炎是主要不良事件。优特克单抗在青少年银屑病中是一种有前景的药物,似乎耐受性良好。在更年轻患者中的最佳监测方案和用法仍有待确定。