Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Glenfield Hospital, Leicester, UK.
Adv Clin Chem. 2012;57:57-97. doi: 10.1016/b978-0-12-394384-2.00003-6.
Asthma is increasing in prevalence worldwide. It is characterized by typical symptoms and variable airway obstruction punctuated with episodes of worsening symptoms known as exacerbations. Underlying this clinical expression of disease is airway inflammation and remodeling. Cytokines and their networks are implicated in the innate and adaptive immune responses driving airway inflammation in asthma and are modulated by host-environment interactions. Asthma is a complex heterogeneous disease, and the paradigm of Th2 cytokine-mediated eosinophilic inflammation as a consequence of allergic sensitization has been challenged and probably represents a subgroup of asthma. Indeed, as attention has switched to the importance of severe asthma, which represents the highest burden both to the patient and health care provider, there is an increasing recognition of inflammatory subphenotypes that are likely to be driven by different cytokine networks. Interestingly, these networks may be specific to aspects of clinical expression as well as inflammatory cell profiles and therefore present novel phenotype-specific therapeutic strategies. Here, we review the breadth of cytokines implicated in the pathogenesis of asthma and focus upon the outcomes of early clinical trials conducted using cytokines or cytokine-blocking therapies.
哮喘在全球范围内的患病率正在增加。它的特征是典型的症状和可变的气道阻塞,并伴有恶化症状的发作,称为加重。这种疾病的临床表现的基础是气道炎症和重塑。细胞因子及其网络参与驱动哮喘气道炎症的先天和适应性免疫反应,并受到宿主-环境相互作用的调节。哮喘是一种复杂的异质性疾病,Th2 细胞因子介导的嗜酸性粒细胞炎症作为过敏致敏的结果的范例受到了挑战,可能代表哮喘的一个亚组。事实上,随着人们对严重哮喘的重视程度不断提高,严重哮喘给患者和医疗保健提供者带来的负担最高,人们越来越认识到可能由不同细胞因子网络驱动的炎症亚表型。有趣的是,这些网络可能与临床表型以及炎症细胞特征有关,因此提出了新的针对特定表型的治疗策略。在这里,我们回顾了参与哮喘发病机制的细胞因子的广泛范围,并重点介绍了使用细胞因子或细胞因子阻断疗法进行的早期临床试验的结果。