苯拉唑马布
免疫学
医学
单克隆抗体
哮喘
单克隆
疾病
嗜酸性
抗体
美波利祖马布
嗜酸性粒细胞
病理
作者
Alessandra Vultaggio,Laura Bergantini,Claudia Crimi,Andrea Matucci,Francesco Menzella,Jan Walter Volk Schroeder,Gianenrico Senna,Paolo Cameli
标识
DOI:10.1080/14712598.2024.2446600
摘要
INTRODUCTION: Benralizumab, a monoclonal IgG antibody, has emerged as a key therapeutic agent in severe asthma by specifically targeting eosinophils, pivotal cells that drive inflammation and tissue damage. Over the past two decades, the availability of such targeted therapies has allowed patients to achieve better disease control. Real-world evidence has consistently demonstrated the effectiveness of benralizumab in managing severe asthma. AREAS COVERED: This paper discusses the kinetic and potential mechanism of action of benralizumab beyond the well-known antibody-dependent cell-mediated cytotoxicity involving natural killer cells. EXPERT OPINION: The available data so far clearly show that reducing eosinophils, one of the main drivers of inflammation and tissue damage in SA, accounts for clinical benefits to these patients. Benralizumab is able to directly reduce tissue levels of eosinophils via multiple mechanisms, and additionally, it is potentially able to modulate the innate immune response. The complex and unique multiple modes of action of benralizumab and its pharmacokinetic features, seem to be the milestone on which the effectiveness of benralizumab is founded.
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