Dermatology Research and Education Foundation, Irvine, CA, USA.
Department of Dermatology, University Hospital of Zürich, Zürich, Switzerland.
J Eur Acad Dermatol Venereol. 2022 Aug;36(8):1171-1177. doi: 10.1111/jdv.18042. Epub 2022 Mar 18.
Anti-drug antibodies (ADAs) can form with certain biological medications, but their clinical significance is not fully understood. ADA formation in psoriasis patients treated with IL-23 inhibitors was evaluated, looking at the incidence of ADAs, impact on clinical outcomes and association with adverse events. A systematic search of PubMed, Cochrane and Embase databases yielded 318 articles, which were manually reviewed. A total of 19 articles met the eligibility criteria. The incidence of ADAs with the IL-23 inhibitors was as follows: 4.1-14.7% with guselkumab, 141-31% with risankizumab and 6.51-18% with tildrakizumab. The incidence of neutralizing antibodies ranged from 01-0.6% with guselkumab, 21-16% with risankizumab and 2.5 to 3.2% with tildrakizumab. There was no evidence of reduced efficacy of psoriasis treatment with ADA presence alone. However, some studies found a reduction in clinical response with high ADA titres or with the presence of neutralizing antibodies. A few studies reported that patients with ADAs to guselkumab and risankizumab had a higher incidence of injection site reactions (ISRs). There do not appear to be other adverse events associated with ADAs with IL-23 inhibitors. Testing for presence of ADAs alone in this patient group does not appear to be predictive of treatment response. Clinically, it may be more productive to test for neutralizing antibodies or ADA titre values, although further investigation is required to show a definitive correlation.
抗药物抗体 (ADAs) 可与某些生物药物形成,但它们的临床意义尚未完全阐明。本研究评估了接受白细胞介素-23 (IL-23) 抑制剂治疗的银屑病患者中 ADA 的形成情况,观察 ADA 的发生率、对临床结局的影响以及与不良事件的关联。通过对 PubMed、Cochrane 和 Embase 数据库进行系统检索,共获得 318 篇文章,并进行了手工审查。共有 19 篇文章符合纳入标准。IL-23 抑制剂的 ADA 发生率如下:古塞库单抗为 4.1-14.7%,里沙利珠单抗为 141-31%,替西单抗为 6.51-18%。古塞库单抗的中和抗体发生率为 0.1-0.6%,里沙利珠单抗为 21-16%,替西单抗为 2.5-3.2%。单独存在 ADA 并不降低银屑病治疗的疗效。然而,一些研究发现,ADA 滴度高或存在中和抗体与临床反应降低有关。一些研究报告称,古塞库单抗和里沙利珠单抗的 ADA 患者注射部位反应 (ISR) 发生率较高。目前似乎没有与 IL-23 抑制剂相关的其他不良反应与 ADA 有关。在该患者群体中单独检测 ADA 的存在似乎不能预测治疗反应。临床上,检测中和抗体或 ADA 滴度可能更有意义,但需要进一步研究以明确相关性。