Department of Dermatology, Shimane University Faculty of Medicine, Izumo, Japan.
Department of Dermatology, Fukuoka University Faculty of Medicine, Fukuoka, Japan.
J Dermatol. 2020 Feb;47(2):128-132. doi: 10.1111/1346-8138.15156. Epub 2019 Nov 24.
Although rare, tuberculosis has been reported with biologic treatment against psoriasis in Japan, a tuberculosis medium-burden country. Mycobacterial infection often develops after a long incubation period and might not have been adequately identified in clinical trials or post-marketing surveillance. To determine the real-world incidence of tuberculosis in psoriatic patients treated with biologics, we conducted a retrospective, multicenter, observational study in 18 facilities in Western Japan. Psoriatic patients who visited a participating facility between 2010 and March 2017 and received biologic reagents were enrolled. Information on sex, age at first biologic treatment, results of interferon-γ release assay (IGRA) for Mycobacterium tuberculosis, treatment history with isoniazid, and onset of active and/or latent tuberculosis was collected. A total of 1117 patients (830 men and 287 women) were enrolled. The mean duration of biologic treatment was 3.54 years. Sixty-five patients (5.8%) showed positive IGRA results at screening. Active tuberculosis developed in two patients after the administration of tumor necrosis factor inhibitors (both involved miliary tuberculosis). Latent tuberculosis was observed in two patients treated with anti-interleukin-12/23p40 antibody. The incidence rate of tuberculosis, including latent tuberculosis, in this survey was 0.36%. Although the incidence rate of tuberculosis was low considering the observation period of biologic treatment, active tuberculosis was found in both the screening-negative group and a screening-positive subject after isoniazid prophylaxis (both miliary tuberculosis), concluding that negative screening or isoniazid treatment does not always assure that an individual has no tuberculosis. Hence, dermatologists still need to pay careful attention to tuberculosis at every patient visit.
虽然罕见,但在日本(一个结核中高负担国家)已有生物制剂治疗银屑病时发生结核的报告。分枝杆菌感染常发生在潜伏期后,在临床试验或上市后监测中可能未得到充分识别。为了确定生物制剂治疗的银屑病患者中结核的真实世界发生率,我们在日本西部的 18 个机构中进行了一项回顾性、多中心、观察性研究。纳入 2010 年至 2017 年 3 月期间在参与机构就诊并接受生物制剂治疗的银屑病患者。收集患者的性别、首次生物治疗时的年龄、结核分枝杆菌干扰素-γ释放试验(IGRA)结果、异烟肼治疗史以及活动性和/或潜伏性结核的发病情况。共纳入 1117 例患者(830 例男性和 287 例女性)。生物制剂治疗的平均时间为 3.54 年。65 例(5.8%)患者在筛查时 IGRA 结果阳性。2 例接受肿瘤坏死因子抑制剂治疗的患者(均为粟粒性结核)发生活动性结核。2 例接受抗白细胞介素-12/23p40 抗体治疗的患者出现潜伏性结核。本次调查中结核(包括潜伏性结核)的发病率为 0.36%。考虑到生物制剂治疗的观察期,结核的发病率较低,但在筛查阴性组和经异烟肼预防治疗的筛查阳性患者(均为粟粒性结核)中均发现活动性结核,这表明阴性筛查或异烟肼治疗并不总能确保个体无结核。因此,皮肤科医生仍需在每次就诊时密切关注结核。