Chiu Hsien-Yi, Wang Ting-Shun, Chan Chih-Chieh, Lin Sung-Jan, Tsai Tsen-Fang
Department of Dermatology, National Taiwan University Hospital, 7 Chung-Shan South Road, Taipei 100, Taiwan.
Acta Derm Venereol. 2015 Jul;95(6):711-6. doi: 10.2340/00015555-2069.
Although anti-drug antibodies against biologics have been associated with decreased clinical efficacy, the immunogenicity of biologics seems to vary between drugs, diseases and ethnicities. This study aims to investigate the predictors for the formation of anti-adalimumab antibodies (AAA) and the clinical consequences of AAA formation. In 53 Chinese psoriatic patients treated with adalimumab, AAA was detected in 50.9%. Differences in Psoriasis Area and Severity Index 75 (PASI75) response rates among patients with and without AAA were significant (44.4% vs. 88.5%; p = 0.001). Patients with AAA had significantly lower trough concentrations of adalimumab than those without AAA. Risk factor analysis showed that treatment interruption, low trough adalimumab concentration, absence of concomitant methotrexate use and biologics switching were associated with a higher AAA titre. The treatment pattern of biologics influences the risk of AAA formation, thereby leading to reduced efficacy of adalimumab.
尽管针对生物制剂的抗药抗体与临床疗效降低有关,但生物制剂的免疫原性似乎因药物、疾病和种族而异。本研究旨在调查抗阿达木单抗抗体(AAA)形成的预测因素以及AAA形成的临床后果。在53例接受阿达木单抗治疗的中国银屑病患者中,AAA检测率为50.9%。有和没有AAA的患者之间银屑病面积和严重程度指数改善75%(PASI75)的应答率差异显著(44.4%对88.5%;p = 0.001)。有AAA的患者阿达木单抗的谷浓度显著低于没有AAA的患者。危险因素分析表明,治疗中断、阿达木单抗谷浓度低、未同时使用甲氨蝶呤和生物制剂转换与较高的AAA滴度相关。生物制剂的治疗模式会影响AAA形成的风险,从而导致阿达木单抗疗效降低。