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PANoptosis为变应性支气管肺曲霉病开辟了新的治疗选择。

PANoptosis opens new treatment options for allergic bronchopulmonary aspergillosis.

作者信息

Smallwood Dalan, Lockey Richard F, Kolliputi Narasaiah

机构信息

Division of Allergy and Immunology, Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa Fla.

出版信息

J Allergy Clin Immunol Glob. 2024 Jul 3;3(4):100298. doi: 10.1016/j.jacig.2024.100298. eCollection 2024 Nov.

DOI:10.1016/j.jacig.2024.100298
PMID:39170913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11338086/
Abstract

BACKGROUND

Allergic bronchopulmonary aspergillosis (ABPA) is a rare airway disorder primarily affecting patients with asthma and cystic fibrosis. Persistent airway inflammation brought on by exacerbates the underlying condition and can cause significant respiratory damage. Treatments center on reducing inflammation with the use of corticosteroids and antifungals. PANoptosis is a new concept in the field of cell death and inflammation that posits the existence of cross talk and a master control system for the 3 programmed cell death (PCD) pathways, namely, apoptosis, pyroptosis, and necroptosis. This concept has revolutionized the understanding of PCD and opened new avenues for its exploration. Studies show that is one of the pathogens that is capable of activating PANoptosis via the Z-DNA binding protein 1 (ZBP1) pathway and plays an active role in the inflammation caused by this organism.

OBJECTIVE

This article explores the nature of inflammation in ABPA and ways in which PCD could lead to novel treatment options.

METHOD

PubMed was used to review the literature surrounding infection-related inflammation and PANoptosis.

RESULTS

There is evidence that apoptosis and pyroptosis protect against induced inflammation, whereas necroptosis promotes inflammation.

CONCLUSION

Experimental medications, in particular, necroptosis inhibitors such as necrosulfonamide and necrostatin-1, should be studied for use in the treatment of ABPA.

摘要

背景

变应性支气管肺曲霉病(ABPA)是一种罕见的气道疾病,主要影响哮喘和囊性纤维化患者。由其引发的持续性气道炎症会加重潜在病情,并可能导致严重的呼吸损伤。治疗主要围绕使用皮质类固醇和抗真菌药物来减轻炎症。全程序坏死是细胞死亡和炎症领域的一个新概念,它假定存在相互作用以及针对三种程序性细胞死亡(PCD)途径(即细胞凋亡、焦亡和坏死性凋亡)的主控系统。这一概念彻底改变了对PCD的理解,并为其探索开辟了新途径。研究表明,[具体病原体未给出]是能够通过Z-DNA结合蛋白1(ZBP1)途径激活全程序坏死的病原体之一,并在该病原体引起的炎症中发挥积极作用。

目的

本文探讨ABPA中炎症的本质以及PCD可能带来新治疗选择的方式。

方法

使用PubMed检索有关[具体病原体未给出]感染相关炎症和全程序坏死的文献。

结果

有证据表明细胞凋亡和焦亡可预防诱导性炎症,而坏死性凋亡则促进炎症。

结论

应研究实验性药物,特别是坏死性凋亡抑制剂,如坏死磺酰胺和坏死他汀-1,用于治疗ABPA。

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变应性支气管肺曲霉病:多学科综述。
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An ALARMINg Type 2 Response in Cystic Fibrosis-The Key to Understanding ABPA?囊性纤维化中一种令人担忧的2型反应——理解ABPA的关键?
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Advances in mechanism and regulation of PANoptosis: Prospects in disease treatment.PANoptosis 的机制和调控研究进展:疾病治疗的前景。
Front Immunol. 2023 Feb 9;14:1120034. doi: 10.3389/fimmu.2023.1120034. eCollection 2023.
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Trends Immunol. 2023 Mar;44(3):201-216. doi: 10.1016/j.it.2023.01.001. Epub 2023 Jan 27.
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