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本文引用的文献

1
Possible Mechanisms of Eosinophil Accumulation in Eosinophilic Pneumonia.嗜酸性粒细胞性肺炎中嗜酸性粒细胞聚集的可能机制。
Biomolecules. 2020 Apr 21;10(4):638. doi: 10.3390/biom10040638.
2
[Construction of mouse CCR3 gene RNAi lentivirus vector and its expression on mast cells].[小鼠CCR3基因RNA干扰慢病毒载体的构建及其在肥大细胞上的表达]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2019 Jul;33(7):628-634. doi: 10.13201/j.issn.1001-1781.2019.07.013.
3
Increasing Prevalence of Allergic Rhinitis in China.中国变应性鼻炎患病率呈上升趋势。
Allergy Asthma Immunol Res. 2019 Mar;11(2):156-169. doi: 10.4168/aair.2019.11.2.156.
4
Tipping the balance: A biased nanobody antagonist of CCR3 with potential for the treatment of eosinophilic inflammation.扭转平衡:一种具有治疗嗜酸性粒细胞炎症潜力的CCR3偏向性纳米抗体拮抗剂。
J Allergy Clin Immunol. 2019 Feb;143(2):552-553. doi: 10.1016/j.jaci.2018.10.052. Epub 2018 Nov 17.
5
Vesicle-associated membrane protein 7-mediated eosinophil degranulation promotes allergic airway inflammation in mice.囊泡相关膜蛋白7介导的嗜酸性粒细胞脱颗粒促进小鼠过敏性气道炎症。
Commun Biol. 2018 Jun 29;1:83. doi: 10.1038/s42003-018-0081-z. eCollection 2018.
6
C‑C chemokine receptor type 3 gene knockout alleviates inflammatory responses in allergic rhinitis model mice by regulating the expression of eosinophil granule proteins and immune factors.C-C 趋化因子受体 3 基因敲除通过调节嗜酸性粒细胞颗粒蛋白和免疫因子的表达缓解变应性鼻炎模型小鼠的炎症反应。
Mol Med Rep. 2018 Oct;18(4):3780-3790. doi: 10.3892/mmr.2018.9380. Epub 2018 Aug 10.
7
[Effect of CCR3 gene knockout on eosinophils in mice].[CCR3基因敲除对小鼠嗜酸性粒细胞的影响]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Dec 20;31(24):1913-1918. doi: 10.13201/j.issn.1001-1781.2017.24.011.
8
Novel peptide nanoparticle-biased antagonist of CCR3 blocks eosinophil recruitment and airway hyperresponsiveness.新型 CCR3 肽纳米颗粒偏向性拮抗剂可阻断嗜酸性粒细胞募集和气道高反应性。
J Allergy Clin Immunol. 2019 Feb;143(2):669-680.e12. doi: 10.1016/j.jaci.2018.05.003. Epub 2018 May 17.
9
[Study on the application of mast cells in the pathogenesis of allergic rhinitis].[肥大细胞在变应性鼻炎发病机制中的应用研究]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2018 Jan 20;32(2):157-160. doi: 10.13201/j.issn.1001-1781.2018.02.019.
10
The effects of a CCR3 inhibitor, AXP1275, on allergen-induced airway responses in adults with mild-to-moderate atopic asthma.CCR3 抑制剂 AXP1275 对轻中度特应性哮喘成人变应原诱导的气道反应的影响。
Clin Exp Allergy. 2018 Apr;48(4):445-451. doi: 10.1111/cea.13114. Epub 2018 Mar 13.

[CCR3基因对呼吸道过敏性疾病相关炎症细胞的影响]

[Effect of CCR3 gene on related inflammatory cells in respiratory allergic diseases].

作者信息

Tang Saiyi, Shu Xinhua

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Jan 5;35(1):80-84. doi: 10.13201/j.issn.2096-7993.2021.01.021.

DOI:10.13201/j.issn.2096-7993.2021.01.021
PMID:33540982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10128548/
Abstract

Respiratory allergic disease mainly include asthma and allergic rhinitis.According to their extremely similarpathogenesis and inflammatory pathological changes,asthma and allergic rhinitis,are regarded as the concept of "one airway, one disease". In recent years, The research on the target of allergens in the pathogenesis mechanism is more in-depth, and the CCR3 gene is a major research target. The study found that the CCR3 gene is an important target gene for the development of respiratory allergic diseases such as allergic rhinitis and asthma. The related inflammatory cells are the main cells responding for the downstream cascade triggered by CCR3 activation, which directly or indirectly cause allergic inflammation through itself or its secretions.Therefore, researches on the roles of CCR3 gene and its related inflammatory cells become hot topics in the clinical treatment of respiratory allergic diseases. This paper reviews the current research progress of respiratory allergic diseases on the basis of intensive literature.

摘要

呼吸道过敏性疾病主要包括哮喘和过敏性鼻炎。由于哮喘和过敏性鼻炎的发病机制及炎症病理变化极为相似,它们被视为“同一气道,同一种疾病”的概念。近年来,对发病机制中过敏原靶点的研究更加深入,CCR3基因是主要研究靶点。研究发现,CCR3基因是过敏性鼻炎和哮喘等呼吸道过敏性疾病发展的重要靶基因。相关炎症细胞是CCR3激活触发的下游级联反应的主要应答细胞,它们通过自身或其分泌物直接或间接引起过敏性炎症。因此,CCR3基因及其相关炎症细胞的作用研究成为呼吸道过敏性疾病临床治疗的热点话题。本文在大量文献的基础上综述了呼吸道过敏性疾病的当前研究进展。