IL33

IL33
  • 文章类型: Journal Article
    过敏性气道疾病(AAD)是呼吸系统疾病的统称,可在暴露于空气中的过敏原后加剧。真菌变应原对AAD的贡献在最近几年已经得到很好的证实。我们使用系统评价和荟萃分析指南的首选报告项目对文献进行了全面审查,以更好地了解气道上皮中真菌过敏反应的机制。确定知识差距,并为未来的研究提出建议。搜索产生了61项最终分析研究。尽管使用的模型和方法存在异质性,我们确定了与真菌过敏有关的主要途径.这些包括蛋白酶激活受体2的激活,EGFR途径,三磷酸腺苷和嘌呤受体依赖性的IL33释放,和氧化应激,驱动粘蛋白表达和杯状细胞化生,Th2细胞因子产生,降低屏障完整性,嗜酸性粒细胞招募,和气道高反应性。然而,有几个知识空白,因此我们建议未来的研究应该集中在使用更生理相关的方法来直接比较主要的过敏性真菌物种,阐明真菌过敏的具体机制,并评估疾病模型中的真菌过敏。这将为疾病管理和未来的干预提供信息。最终减轻疾病负担。
    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.
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