Crisford Helena, Sapey Elizabeth, Rogers Geraint B, Taylor Steven, Nagakumar Prasad, Lokwani Ravi, Simpson Jodie L
Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Thorax. 2021 Feb 25;76(8):835-44. doi: 10.1136/thoraxjnl-2020-215986.
Airway inflammation plays a key role in asthma pathogenesis but is heterogeneous in nature. There has been significant scientific discovery with regard to type 2-driven, eosinophil-dominated asthma, with effective therapies ranging from inhaled corticosteroids to novel biologics. However, studies suggest that approximately 1 in 5 adults with asthma have an increased proportion of neutrophils in their airways. These patients tend to be older, have potentially pathogenic airway bacteria and do not respond well to classical therapies. Currently, there are no specific therapeutic options for these patients, such as neutrophil-targeting biologics.Neutrophils comprise 70% of the total circulatory white cells and play a critical defence role during inflammatory and infective challenges. This makes them a problematic target for therapeutics. Furthermore, neutrophil functions change with age, with reduced microbial killing, increased reactive oxygen species release and reduced production of extracellular traps with advancing age. Therefore, different therapeutic strategies may be required for different age groups of patients.The pathogenesis of neutrophil-dominated airway inflammation in adults with asthma may reflect a counterproductive response to the defective neutrophil microbial killing seen with age, resulting in bystander damage to host airway cells and subsequent mucus hypersecretion and airway remodelling. However, in children with asthma, neutrophils are less associated with adverse features of disease, and it is possible that in children, neutrophils are less pathogenic.In this review, we explore the mechanisms of neutrophil recruitment, changes in cellular function across the life course and the implications this may have for asthma management now and in the future. We also describe the prevalence of neutrophilic asthma globally, with a focus on First Nations people of Australia, New Zealand and North America.
气道炎症在哮喘发病机制中起关键作用,但本质上具有异质性。关于2型驱动、嗜酸性粒细胞为主的哮喘已有重大科学发现,有效治疗方法从吸入性糖皮质激素到新型生物制剂不等。然而,研究表明,约五分之一的成年哮喘患者气道中嗜中性粒细胞比例增加。这些患者往往年龄较大,气道中可能存在致病细菌,且对传统疗法反应不佳。目前,针对这些患者没有特定的治疗选择,如靶向嗜中性粒细胞的生物制剂。嗜中性粒细胞占循环白细胞总数的70%,在炎症和感染挑战中起关键防御作用。这使其成为治疗的难题靶点。此外,嗜中性粒细胞功能随年龄变化,随着年龄增长,微生物杀伤能力降低,活性氧释放增加,细胞外陷阱产生减少。因此,不同年龄组的患者可能需要不同的治疗策略。成年哮喘患者中嗜中性粒细胞为主的气道炎症发病机制可能反映了对随着年龄增长出现的嗜中性粒细胞微生物杀伤缺陷的适得其反的反应,导致对宿主气道细胞的旁观者损伤以及随后的黏液分泌过多和气道重塑。然而,在儿童哮喘患者中,嗜中性粒细胞与疾病的不良特征关联较小,儿童的嗜中性粒细胞致病性可能较低。在本综述中,我们探讨了嗜中性粒细胞募集的机制、整个生命过程中细胞功能的变化及其对当前和未来哮喘管理的影响。我们还描述了全球嗜中性粒细胞性哮喘的患病率,重点关注澳大利亚、新西兰和北美的原住民。