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肥大细胞在变应性鼻炎中的作用。

The role of mast cells in allergic rhinitis.

作者信息

Zhang Jin, Xie Xiaofei, Ma Ruixia, Liu Peng

机构信息

Department of Otolaryngology, Yibin Second People's Hospital, Yibin, China.

Department of Paediatric, Ziyang Traditional Chinese Medicine Hospital, Ziyang, China.

出版信息

PeerJ. 2025 Jul 30;13:e19734. doi: 10.7717/peerj.19734. eCollection 2025.

DOI:10.7717/peerj.19734
PMID:40755802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12317689/
Abstract

INTRODUCTION

In recent decades, mast cells and their mediators have been increasingly recognized as central players in the pathogenesis of allergic rhinitis (AR), a complex chronic nasal disease characterized by pathological changes influenced by genetic factors, various immune cells, and environmental exposures. Mast cells are pivotal in allergic reactions, orchestrating inflammation and airway contraction through the secretion of diverse mediators. Prominent among these mediators are histamine and bioactive lipids, whose physiological effects are prominently observed during the acute phase of allergic reactions. The accumulation of mast cells in specific areas of allergic rhinitis may correlate with the disease's phenotype, progression, and severity. experiments in mice have demonstrated that mast cells develop from mast cell progenitor cells, which are induced by inflammatory stimuli and subsequently migrate to the airway. Human mast cell progenitor cells have been identified in the bloodstream, with a high proportion potentially reflecting the persistent pathological changes associated with allergic rhinitis. The primary activation of mast cells in allergic rhinitis occurs via the cross-linking of IgE high-affinity receptors (Fc RI) mediated by IgE in conjunction with allergens. However, mast cells can also be activated by a variety of other stimuli, including toll-like receptors and MAS-related G protein-coupled receptor X2.

RATIONALE FOR THIS REVIEW

Despite the substantial progress in understanding the role of mast cells in allergic rhinitis, several critical gaps remain in our knowledge. The complex interplay between mast cells, their mediators, and the immune system in the context of AR is still not fully elucidated. Moreover, the specific mechanisms underlying the recruitment and activation of mast cell progenitor cells in the nasal mucosa remain poorly understood. Addressing these gaps is essential for developing more effective therapeutic strategies for allergic rhinitis. This review aims to provide a comprehensive and up-to-date synthesis of the current literature on the role and development of mast cells and their progenitor cells in allergic rhinitis, including the activation pathways implicated in the pathogenesis.

TARGET AUDIENCE

This review is intended for a broad audience, including researchers in the fields of immunology, allergy, and respiratory medicine, as well as clinicians who manage patients with allergic rhinitis. By summarizing the latest findings and highlighting the unresolved questions, this review aims to serve as a valuable reference for future research directions in mast cells and allergic rhinitis, ultimately contributing to improved patient care and outcomes.

摘要

引言

近几十年来,肥大细胞及其介质在变应性鼻炎(AR)发病机制中的核心作用日益受到认可。变应性鼻炎是一种复杂的慢性鼻病,其病理变化受遗传因素、多种免疫细胞和环境暴露的影响。肥大细胞在过敏反应中起关键作用,通过分泌多种介质来协调炎症反应和气道收缩。这些介质中突出的是组胺和生物活性脂质,其生理效应在过敏反应急性期显著可见。肥大细胞在变应性鼻炎特定区域的积聚可能与疾病的表型、进展和严重程度相关。小鼠实验表明,肥大细胞由肥大细胞祖细胞发育而来,这些祖细胞受炎症刺激诱导,随后迁移至气道。已在血液中鉴定出人类肥大细胞祖细胞,其高比例可能反映了与变应性鼻炎相关的持续病理变化。变应性鼻炎中肥大细胞的主要激活是通过IgE与变应原结合介导的IgE高亲和力受体(Fc RI)交联实现的。然而,肥大细胞也可被多种其他刺激激活,包括Toll样受体和MAS相关G蛋白偶联受体X2。

本综述的理论依据

尽管在理解肥大细胞在变应性鼻炎中的作用方面取得了重大进展,但我们的知识仍存在一些关键空白。在变应性鼻炎背景下,肥大细胞、其介质与免疫系统之间复杂的相互作用仍未完全阐明。此外,鼻黏膜中肥大细胞祖细胞募集和激活的具体机制仍知之甚少。填补这些空白对于开发更有效的变应性鼻炎治疗策略至关重要。本综述旨在全面、最新地综合当前关于肥大细胞及其祖细胞在变应性鼻炎中的作用和发育的文献,包括发病机制中涉及的激活途径。

目标受众

本综述面向广泛的受众,包括免疫学、过敏和呼吸医学领域的研究人员,以及治疗变应性鼻炎患者的临床医生。通过总结最新发现并突出未解决的问题,本综述旨在为肥大细胞和变应性鼻炎未来的研究方向提供有价值的参考,最终有助于改善患者护理和治疗结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4479/12317689/49c8f3823449/peerj-13-19734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4479/12317689/49c8f3823449/peerj-13-19734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4479/12317689/49c8f3823449/peerj-13-19734-g001.jpg

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