Division of Dermatology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York.
JAMA Dermatol. 2013 Dec;149(12):1410-3. doi: 10.1001/jamadermatol.2013.5728.
Ustekinumab is a human monoclonal antibody that binds to the shared p40 subunit of interleukin (IL) 12 and IL-23. It is approved in the United States for adults (>18 years) with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy. In 1 phase 2 trial of ustekinumab for treatment of psoriatic arthritis, joint disease improved.
We report 4 cases of ustekinumab monotherapy for plaque psoriasis that resulted in disabling flares of known psoriatic arthritis or unmasked previously occult joint disease. In all of our cases, psoriasis improved dramatically with ustekinumab therapy while psoriatic arthritis flared.
Despite early results of a phase 2 ustekinumab trial suggesting efficacy for both plaque psoriasis and psoriatic arthritis, our case series raises concern that ustekinumab may unmask or aggravate joint disease in selected patients. These data underscore the need for further investigation of ustekinumab's effects on psoriatic arthritis.
乌司奴单抗是一种人源化单克隆抗体,可与白细胞介素(IL)12 和 IL-23 的共享 p40 亚单位结合。它在美国被批准用于治疗适合光疗或系统治疗的中重度斑块型银屑病成人(>18 岁)。在乌司奴单抗治疗银屑病关节炎的 2 期 1 项试验中,关节疾病得到改善。
我们报告了 4 例单用乌司奴单抗治疗斑块型银屑病的病例,导致已知的银屑病关节炎严重发作或先前隐匿性关节病显现。在我们所有的病例中,银屑病随着乌司奴单抗治疗而显著改善,而银屑病关节炎却恶化了。
尽管 2 期乌司奴单抗试验的早期结果表明其对斑块型银屑病和银屑病关节炎均有效,但我们的病例系列研究引起了人们的关注,即乌司奴单抗可能会在某些患者中显现或加重关节疾病。这些数据强调了进一步研究乌司奴单抗对银屑病关节炎影响的必要性。