a argenx BVBA , Zwijnaarde , Belgium.
b VIB-UGent Center for Inflammation Research , Ghent , Belgium.
MAbs. 2018 Jan;10(1):34-45. doi: 10.1080/19420862.2017.1392425. Epub 2017 Nov 14.
Asthma affects more than 300 million people worldwide and poses a large socioeconomic burden, particularly in the 5% to 10% of severe asthmatics. So far, each entry of new biologics in clinical trials has led to high expectations for treating all severe asthma forms, but the outcome has only been successful if the biologic, as add-on treatment, targeted specific patient subgroups. Indeed, we now realize that asthma is a heterogeneous disease with multiple phenotypes, based on distinct pathophysiological mechanisms, called endotypes. Thus, asthma therapy is gradually moving to a personalized medicine approach, tailored to individual's asthma endotypes identified through biomarkers. Here, we review the clinical efficacy of antibody-related therapeutics undergoing clinical trials, or those already approved, for the treatment of severe type 2 asthma. Biologics targeting type 2 cytokines have shown consistent efficacy, especially in patients with evidence of type 2 inflammation, suggesting that the future of asthma biologics is promising.
哮喘影响着全球超过 3 亿人,并造成了巨大的社会经济负担,尤其是在 5%至 10%的重度哮喘患者中。到目前为止,临床试验中的每一种新型生物制剂的进入都为治疗所有重度哮喘形式带来了很高的期望,但如果生物制剂作为附加治疗,针对特定的患者亚组,其结果才是成功的。事实上,我们现在意识到哮喘是一种具有多种表型的异质性疾病,这些表型基于不同的病理生理机制,称为表型。因此,哮喘治疗正逐渐转向个体化药物治疗方法,根据通过生物标志物识别的个体的哮喘表型进行定制。在这里,我们回顾了正在进行临床试验或已获得批准的针对 2 型重度哮喘治疗的抗体相关治疗药物的临床疗效。针对 2 型细胞因子的生物制剂已显示出一致的疗效,尤其是在有 2 型炎症证据的患者中,这表明哮喘生物制剂的未来前景广阔。