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一项范围综述:驱动肺上皮细胞对真菌过敏原产生过敏性炎症反应的细胞机制是什么?

A scoping review: What are the cellular mechanisms that drive the allergic inflammatory response to fungal allergens in the lung epithelium?

作者信息

Goode Emma-Jane, Marczylo Emma

机构信息

Toxicology Department, UK Health Security Agency, Chilton, UK.

出版信息

Clin Transl Allergy. 2023 Jun;13(6):e12252. doi: 10.1002/clt2.12252.

Abstract

Allergic airway disease (AAD) is a collective term for respiratory disorders that can be exacerbated upon exposure to airborne allergens. The contribution of fungal allergens to AAD has become well established over recent years. We conducted a comprehensive review of the literature using Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to better understand the mechanisms involved in the allergic response to fungi in airway epithelia, identify knowledge gaps and make recommendations for future research. The search resulted in 61 studies for final analysis. Despite heterogeneity in the models and methods used, we identified major pathways involved in fungal allergy. These included the activation of protease-activated receptor 2, the EGFR pathway, adenosine triphosphate and purinergic receptor-dependent release of IL33, and oxidative stress, which drove mucin expression and goblet cell metaplasia, Th2 cytokine production, reduced barrier integrity, eosinophil recruitment, and airway hyperresponsiveness. However, there were several knowledge gaps and therefore we recommend future research should focus on the use of more physiologically relevant methods to directly compare key allergenic fungal species, clarify specific mechanisms of fungal allergy, and assess the fungal allergy in disease models. This will inform disease management and future interventions, ultimately reducing the burden of disease.

摘要

变应性气道疾病(AAD)是一类呼吸道疾病的统称,接触空气中的过敏原会使其加重。近年来,真菌过敏原在AAD中的作用已得到充分证实。我们按照系统评价和Meta分析的首选报告项目指南对文献进行了全面综述,以更好地了解气道上皮对真菌过敏反应的相关机制,找出知识空白,并为未来研究提出建议。检索结果为61项可供最终分析的研究。尽管所用模型和方法存在异质性,但我们确定了真菌过敏的主要途径。这些途径包括蛋白酶激活受体2的激活、表皮生长因子受体(EGFR)途径、三磷酸腺苷和嘌呤能受体依赖性白细胞介素33的释放,以及氧化应激,后者导致粘蛋白表达和杯状细胞化生、Th2细胞因子产生、屏障完整性降低、嗜酸性粒细胞募集和气道高反应性。然而,仍存在一些知识空白,因此我们建议未来的研究应侧重于使用更具生理相关性的方法,以直接比较关键的致敏真菌种类,阐明真菌过敏的具体机制,并在疾病模型中评估真菌过敏。这将为疾病管理和未来干预提供依据,最终减轻疾病负担。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff61/10234180/9b34e0d3ccd7/CLT2-13-e12252-g007.jpg

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