Clinical Context

Severe asthma is a chronic inflammatory disorder of the airways that can lead to significant morbidity, including decreased quality of life, fixed airway obstruction, hospitalization, and even mortality [1]. Traditional treatments, such as inhaled corticosteroids and bronchodilators, may not adequately control symptoms for all patients, leading to the need for biologic therapies. Biologics target specific pathways involved in the pathophysiology of asthma, offering a tailored approach to treatment. Mepolizumab and benralizumab target interleukin-5 (IL-5), a key cytokine in eosinophilic inflammation, while dupilumab blocks interleukin-4 (IL-4) and interleukin-13 (IL-13) signaling, which are pivotal in allergic inflammation. Tezepelumab, a newer entrant, inhibits thymic stromal lymphopoietin (TSLP), further expanding the therapeutic options for patients with severe asthma [3]. Depemokimab, another emerging biologic, is being evaluated for its efficacy in eosinophilic asthma [2]. As these biologics become more integrated into treatment protocols, understanding their distinct mechanisms and clinical data is essential for optimizing patient outcomes.