Bajpai Jyoti, Kant Surya, Matera Maria Gabriella, Cazzola Mario
Department of Respiratory Medicine King George's Medical University, UP Lucknow, 226003, India.
Unit of Pharmacology, Department of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Respir Med. 2025 Sep;246:108243. doi: 10.1016/j.rmed.2025.108243. Epub 2025 Jul 3.
Brensocatib is an oral inhibitor of dipeptidyl peptidase 1, an enzyme that activates neutrophil serine proteases. Its potential to reduce neutrophil-driven inflammation has generated interest across a range of chronic inflammatory and respiratory conditions, particularly non-cystic fibrosis (CF) bronchiectasis. As the body of evidence supporting brensocatib continues to expand, there is a clear need for a comprehensive, rigorous, and practical narrative review to consolidate current knowledge and highlight gaps for future research. The aim of this narrative review was to systematically examine and synthesize the existing literature on brensocatib, including its pharmacology, therapeutic applications, clinical trial outcomes, safety profile, and ongoing research efforts. A systematic search was performed across major databases, EMBASE, MEDLINE, Scopus, Web of Science, Google Scholar, and ClinicalTrials.gov, through April 2025. Studies involving brensocatib in preclinical or clinical contexts were thoroughly reviewed to evaluate its efficacy and safety. Data were extracted on study design, population, dosage, outcomes, adverse events (AEs), and key findings. The most extensively studied indication was non-CF bronchiectasis, where brensocatib demonstrated a reduction in exacerbation rates and neutrophil protease activity. Preliminary evidence also suggests potential applications in CF, chronic obstructive pulmonary disease, and other neutrophilic conditions. An evaluation of the safety data indicates that the AEs reported are generally mild to moderate in severity. Brensocatib demonstrates potential as a novel anti-inflammatory therapy targeting neutrophil-mediated disease mechanisms. Further research is needed to evaluate its long-term efficacy, safety across a broader population, and its role in combination therapies.
布瑞索替布是一种二肽基肽酶1的口服抑制剂,二肽基肽酶1是一种可激活中性粒细胞丝氨酸蛋白酶的酶。其降低中性粒细胞驱动的炎症的潜力已在一系列慢性炎症和呼吸系统疾病中引起关注,尤其是非囊性纤维化(CF)支气管扩张症。随着支持布瑞索替布的证据不断增加,显然需要进行全面、严谨且实用的叙述性综述,以巩固现有知识并突出未来研究的空白。本叙述性综述的目的是系统地审查和综合关于布瑞索替布的现有文献,包括其药理学、治疗应用、临床试验结果、安全性概况以及正在进行的研究工作。截至2025年4月,在主要数据库EMBASE、MEDLINE、Scopus、科学网、谷歌学术和临床试验.gov上进行了系统检索。对涉及布瑞索替布的临床前或临床研究进行了全面审查,以评估其疗效和安全性。提取了关于研究设计、人群、剂量、结果、不良事件(AE)和主要发现的数据。研究最广泛的适应症是非CF支气管扩张症,布瑞索替布在该病症中显示出加重率和中性粒细胞蛋白酶活性降低。初步证据还表明其在CF、慢性阻塞性肺疾病和其他嗜中性粒细胞相关病症中的潜在应用。对安全性数据的评估表明,报告的AE严重程度一般为轻度至中度。布瑞索替布显示出作为一种针对中性粒细胞介导的疾病机制的新型抗炎疗法的潜力。需要进一步研究来评估其长期疗效、在更广泛人群中的安全性以及其在联合治疗中的作用。