Solomonidi Nicky, Vlachoyiannopoulos Panayiotis G, Pappa Maria, Liantinioti Georgia, Ktena Sofia, Theotikos Evangelos, Elezoglou Antonia, Netea Mihai G, Giamarellos-Bourboulis Evangelos J
4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
Department of Pathophysiology, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
iScience. 2023 Aug 19;26(9):107670. doi: 10.1016/j.isci.2023.107670. eCollection 2023 Sep 15.
Increased concentrations of interleukin (IL)-1α have been recently described in tissues of patients with systemic sclerosis (SSc) suggesting that IL-1α inhibition may be a target for treatment. We conducted a double-blind, placebo-controlled study to assess the safety and efficacy of the fully humanized IL-1α blocking monoclonal antibody bermekimab in SSc. To evaluate response to treatment, we developed the score of inhibition of progression of SSc which was validated using the CRISS index and the modified CRISS index. The primary endpoint was met in 80% of bermekimab-treated patients vs. 20% of placebo-treated patients (p: 0.023). Most of efficacy was found for increase of carbon monoxide lung diffusion capacity. Production of IL-1α and TNF by circulating mononuclear cells was decreased and the absolute count of CD42/Cd62-platelets was decreased. Results suggest that bermekimab is a promising treatment for SSc.
最近有研究表明,系统性硬化症(SSc)患者组织中白细胞介素(IL)-1α浓度升高,这表明抑制IL-1α可能是一种治疗靶点。我们进行了一项双盲、安慰剂对照研究,以评估全人源化IL-1α阻断单克隆抗体bermekimab治疗SSc的安全性和有效性。为了评估治疗反应,我们制定了SSc病情进展抑制评分,并使用CRISS指数和改良CRISS指数进行了验证。bermekimab治疗的患者中有80%达到了主要终点,而安慰剂治疗的患者中这一比例为20%(p = 0.023)。大部分疗效体现在一氧化碳肺扩散能力的提高上。循环单核细胞产生的IL-1α和TNF减少,CD42/Cd62-血小板的绝对计数也减少。结果表明,bermekimab是一种有前景的SSc治疗药物。