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嗜酸性粒细胞性呼吸系统疾病及生物制剂的影响

Eosinophilic respiratory disorders and the impact of biologics.

作者信息

Bernstein Joshua S, Wechsler Michael E

机构信息

National Jewish Health, Denver, Colorado, USA.

出版信息

Curr Opin Pulm Med. 2023 May 1;29(3):202-208. doi: 10.1097/MCP.0000000000000951. Epub 2023 Mar 3.

DOI:10.1097/MCP.0000000000000951
PMID:36866734
Abstract

PURPOSE OF REVIEW

Eosinophils are involved in combating parasitic, bacterial, viral infections as well as certain malignancies. However, they are also implicated in an array of upper and lower respiratory disease states. Through a deeper understanding of disease pathogenesis, targeted biologic therapies have revolutionized glucocorticoid sparing treatment of eosinophilic respiratory diseases. This review will focus on the impact of novel biologics on the management of asthma, eosinophilic granulomatosis with polyangiitis, allergic bronchopulmonary aspergillosis (ABPA), hypereosinophilic syndrome (HES) and chronic rhinosinusitis with nasal polyposis (CRSwNP).

RECENT FINDINGS

Key immunologic pathways affecting Type 2 inflammation through immunoglobulin E (IgE), interleukin (IL-4), IL-5, IL-13, and upstream alarmins such as thymic stromal lymphopoietin (TSLP), have led to novel drug developments. We explore the mechanism of action for Omalizumab, Mepolizumab, Benralizumab, Reslizumab, Dupilumab, and Tezepelumab, their respective Food and Drug Administration (FDA) indications, and biomarkers affecting treatment decisions. We also highlight investigational therapeutics that are likely to impact the future management of eosinophilic respiratory diseases.

SUMMARY

Insight into the biology of eosinophilic respiratory diseases has been critical for understanding disease pathogenesis and has contributed to the development of effective eosinophil-targeted biologic interventions.

摘要

综述目的

嗜酸性粒细胞参与对抗寄生虫、细菌、病毒感染以及某些恶性肿瘤。然而,它们也与一系列上、下呼吸道疾病状态有关。通过对疾病发病机制的更深入了解,靶向生物疗法彻底改变了嗜酸性粒细胞性呼吸道疾病的糖皮质激素节省治疗。本综述将重点关注新型生物制剂对哮喘、嗜酸性肉芽肿性多血管炎、变应性支气管肺曲霉病(ABPA)、高嗜酸性粒细胞综合征(HES)和伴鼻息肉的慢性鼻-鼻窦炎(CRSwNP)治疗的影响。

最新发现

通过免疫球蛋白E(IgE)、白细胞介素(IL-4)、IL-5、IL-13以及上游警报素如胸腺基质淋巴细胞生成素(TSLP)影响2型炎症的关键免疫途径,已促成了新型药物的研发。我们探讨了奥马珠单抗、美泊利单抗、贝那利珠单抗、瑞利珠单抗、度普利尤单抗和替泽佩尤单抗的作用机制、它们各自的美国食品药品监督管理局(FDA)适应证以及影响治疗决策的生物标志物。我们还重点介绍了可能会影响嗜酸性粒细胞性呼吸道疾病未来治疗的研究性疗法。

总结

深入了解嗜酸性粒细胞性呼吸道疾病的生物学特性对于理解疾病发病机制至关重要,并有助于开发有效的嗜酸性粒细胞靶向生物干预措施。

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