Ren Lei, Zhang Nan, Zhang Luo, Bachert Claus
Upper Airways Research Laboratory, Ghent University, Ghent, Belgium.
Department of Allergy, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
World Allergy Organ J. 2019 Aug 9;12(8):100050. doi: 10.1016/j.waojou.2019.100050. eCollection 2019 Aug.
Chronic rhinosinusitis with nasal polyps (CRSwNP) is a complex upper airway disease affecting up to 11% of the population of Western Europe. In these western countries, 85% of the CRSwNP disease reveals a type 2 inflammatory pattern. In the last 15 years, several randomized double-blind studies on monoclonal antibodies in CRSwNP were performed. These studies demonstrated for the first time that biologics targeting type 2 immune reactions might be successful in nasal polyps. The target proteins, interleukin (IL)-4, IL-5, IL-13, and IgE were previously identified as key mediators in studies using nasal polyp tissues to measure and to interact in ex-vivo settings. No biomarkers have been identified to predict response to a specific biologic or to monitor treatment success. These studies were characterized by small numbers of patients and heterogeneous populations. They did, however, pave the way for currently performed and analyzed phase 3 studies, which will possibly lead to the registration of the first biologic drug with the indication CRSwNP. The studies already provide indications on the effects to be expected from those biologics; the results of phase-3 studies in larger populations will be decisive for the indications, patient selection, and finally the stopping rules for those drugs in subjects with severe nasal polyps, in whom the current standard of care including topical and oral glucocorticosteroids, antibiotics and surgical procedures failed to control the disease. We may expect that those biologics will open new perspectives for those patients with severe polyposis with, but also independent of asthma, allowing to avoid the possible adverse events resulting from systemic glucocorticosteroids and surgery.
伴鼻息肉的慢性鼻-鼻窦炎(CRSwNP)是一种复杂的上呼吸道疾病,影响着高达11%的西欧人口。在这些西方国家,85%的CRSwNP疾病呈现2型炎症模式。在过去15年里,针对CRSwNP的单克隆抗体进行了多项随机双盲研究。这些研究首次证明,靶向2型免疫反应的生物制剂可能对鼻息肉有效。在使用鼻息肉组织进行体外测量和相互作用的研究中,目标蛋白白细胞介素(IL)-4、IL-5、IL-13和IgE先前被确定为关键介质。尚未确定能够预测对特定生物制剂的反应或监测治疗成功的生物标志物。这些研究的特点是患者数量少且人群异质性大。然而,它们为目前正在进行和分析的3期研究铺平了道路,这可能会导致首个有CRSwNP适应症的生物药物获批。这些研究已经提供了关于这些生物制剂预期效果的线索;在更大人群中进行的3期研究结果将对适应症、患者选择以及最终对那些严重鼻息肉患者使用这些药物的停药规则起到决定性作用,在这些患者中,包括局部和口服糖皮质激素、抗生素及外科手术在内的当前标准治疗方法未能控制病情。我们可以预期,这些生物制剂将为那些患有严重息肉病且伴有或不伴有哮喘的患者开辟新的前景,使他们能够避免全身糖皮质激素和手术可能带来的不良事件。