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针对不适合阿达木单抗的中重度化脓性汗腺炎患者,MABp1 靶向白介素-1α:一项随机研究。

MABp1 Targeting IL-1α for Moderate to Severe Hidradenitis Suppurativa Not Eligible for Adalimumab: A Randomized Study.

机构信息

Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Greece.

XBiotech, Austin, Texas, USA.

出版信息

J Invest Dermatol. 2018 Apr;138(4):795-801. doi: 10.1016/j.jid.2017.10.030. Epub 2017 Nov 10.

DOI:10.1016/j.jid.2017.10.030
PMID:29129600
Abstract

Patients with moderate to severe hidradenitis suppurativa failing adalimumab therapy, or those ineligible to receive it, remain a population with an unmet need. Twenty patients not eligible for adalimumab were randomized to receive 12 weeks of blind treatment with placebo or MABp1, a true human antibody targeting IL-1α. Hidradenitis suppurativa clinical response score at week 12 was the primary endpoint. The primary endpoint was met in 10% and 60% of placebo- and MABp1-treated patients, respectively (odds ratio = 13.50, 95% confidence interval = 1.19-152.51). Clinical efficacy was maintained at 24 weeks in 0% and 40%. Improvement in the visual analog scale was reported by 20% and 85.7%, respectively, of patients failing previous anti-TNF treatment. Ultrasonography showed decreased neovascularization and lesion skin depth in the MABp1 group. MABp1 treatment was associated with decrease of circulating IL-8 and of stimulated production of IL-8 by whole blood. Whole blood production for hBD-2 was negatively associated with changes on ultrasonography in the placebo group but not in the MABp1 group. MABp1 is a promising treatment for patients with hidradenitis suppurativa not eligible for adalimumab. Inhibition of neovascularization and modulation of the production of IL-8 and hBD-2 are suggested mechanisms of action.

摘要

对于阿达木单抗治疗失败或不适合接受阿达木单抗治疗的中重度化脓性汗腺炎患者,他们的需求仍未得到满足。20 名不适合阿达木单抗治疗的患者被随机分配接受为期 12 周的安慰剂或 MABp1 盲法治疗,MABp1 是一种针对白细胞介素 1α 的真正人源抗体。第 12 周的化脓性汗腺炎临床应答评分是主要终点。安慰剂和 MABp1 治疗组分别有 10%和 60%的患者达到主要终点(比值比=13.50,95%置信区间=1.19-152.51)。在 24 周时,0%和 40%的患者保持临床疗效。在之前接受过抗 TNF 治疗失败的患者中,分别有 20%和 85.7%的患者报告了视觉模拟量表的改善。超声检查显示 MABp1 组的新生血管减少和病变皮肤深度降低。MABp1 治疗与循环白细胞介素 8 和全血刺激产生的白细胞介素 8 减少有关。全血 hBD-2 的产生与安慰剂组的超声变化呈负相关,但与 MABp1 组无关。MABp1 是一种有前途的治疗方法,适用于不适合阿达木单抗治疗的化脓性汗腺炎患者。抑制新生血管形成和调节白细胞介素 8 和 hBD-2 的产生被认为是其作用机制。

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