Palomares Óscar, Sánchez-Ramón Silvia, Dávila Ignacio, Prieto Luis, Pérez de Llano Luis, Lleonart Marta, Domingo Christian, Nieto Antonio
Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University of Madrid, 28040 Madrid, Spain.
Department of Clinical Immunology and Health Research Institute of the Hospital Clínico San Carlos (IdISSC), Hospital Clínico San Carlos, 28040 Madrid, Spain.
Int J Mol Sci. 2017 Jun 21;18(6):1328. doi: 10.3390/ijms18061328.
Asthma is an airway disease characterised by chronic inflammation with intermittent or permanent symptoms including wheezing, shortness of breath, chest tightness, and cough, which vary in terms of their occurrence, frequency, and intensity. The most common associated feature in the airways of patients with asthma is airway inflammation. In recent decades, efforts have been made to characterise the heterogeneous clinical nature of asthma. The interest in improving the definitions of asthma phenotypes and endotypes is growing, although these classifications do not always correlate with prognosis nor are always appropriate therapeutic approaches. Attempts have been made to identify the most relevant molecular and cellular biomarkers underlying the immunopathophysiological mechanisms of the disease. For almost 50 years, immunoglobulin E (IgE) has been identified as a central factor in allergic asthma, due to its allergen-specific nature. Many of the mechanisms of the inflammatory cascade underlying allergic asthma have already been elucidated, and IgE has been shown to play a fundamental role in the triggering, development, and chronicity of the inflammatory responses within the disease. Blocking IgE with monoclonal antibodies such as omalizumab have demonstrated their efficacy, effectiveness, and safety in treating allergic asthma. A better understanding of the multiple contributions of IgE to the inflammatory continuum of asthma could contribute to the development of novel therapeutic strategies for the disease.
哮喘是一种气道疾病,其特征为慢性炎症,伴有间歇性或持续性症状,包括喘息、气短、胸闷和咳嗽,这些症状在发作、频率和强度方面各不相同。哮喘患者气道中最常见的相关特征是气道炎症。近几十年来,人们一直在努力描述哮喘的异质性临床本质。尽管这些分类并不总是与预后相关,也并非总是适用的治疗方法,但对改善哮喘表型和内型定义的兴趣与日俱增。人们试图确定该疾病免疫病理生理机制背后最相关的分子和细胞生物标志物。近50年来,免疫球蛋白E(IgE)因其过敏原特异性,已被确定为过敏性哮喘的核心因素。过敏性哮喘炎症级联反应的许多机制已经阐明,并且IgE已被证明在该疾病炎症反应的触发、发展和慢性化过程中起重要作用。用奥马珠单抗等单克隆抗体阻断IgE已证明其在治疗过敏性哮喘方面的疗效、有效性和安全性。更好地理解IgE对哮喘炎症连续体的多种作用可能有助于开发该疾病的新型治疗策略。