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哮喘的实验小鼠模型与 CD4 T 细胞分析。

Experimental Mouse Models of Asthma and Analysis of CD4 T Cells.

机构信息

National Heart and Lung Institute, Imperial College London, London, UK.

出版信息

Methods Mol Biol. 2021;2285:329-348. doi: 10.1007/978-1-0716-1311-5_25.

DOI:10.1007/978-1-0716-1311-5_25
PMID:33928563
Abstract

Asthma is a highly prevalent lung disease, characterized by airway dysfunction and chronic inflammation. Asthma occurs in both children and adults, but frequently originates in early life. Heterogeneous asthma phenotypes exist, but Th2 cells are key players in a large proportion of cases, while other CD4+ T cell subsets are also implicated in driving and limiting pathology. In this chapter, we describe methods for establishing allergic airway disease to model asthma in adult and neonatal mice, along with protocols for measuring key disease parameters and quantifying and phenotyping CD4+ T cell subtypes.

摘要

哮喘是一种高发肺部疾病,其特征为气道功能障碍和慢性炎症。哮喘可发生于儿童和成人,但通常在生命早期就已出现。哮喘存在多种表型,但 Th2 细胞是大多数情况下的关键致病因素,其他 CD4+T 细胞亚群也参与了疾病的发生和发展。在本章中,我们将描述在成年和新生小鼠中建立变应性气道疾病模型来模拟哮喘的方法,以及测量关键疾病参数、定量和表型分析 CD4+T 细胞亚群的方案。

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1
Experimental Mouse Models of Asthma and Analysis of CD4 T Cells.哮喘的实验小鼠模型与 CD4 T 细胞分析。
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2
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IL-2 receptor beta-chain signaling controls immunosuppressive CD4+ T cells in the draining lymph nodes and lung during allergic airway inflammation in vivo.白细胞介素-2受体β链信号传导在体内过敏性气道炎症期间控制引流淋巴结和肺中的免疫抑制性CD4 + T细胞。
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引用本文的文献

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本文引用的文献

1
Pulmonary Group 2 Innate Lymphoid Cell Phenotype Is Context Specific: Determining the Effect of Strain, Location, and Stimuli.肺脏 2 型固有淋巴细胞表型具有特定的背景依赖性:确定其受菌株、位置和刺激因素的影响。
Front Immunol. 2020 Jan 22;10:3114. doi: 10.3389/fimmu.2019.03114. eCollection 2019.
2
New Therapies for Emerging Endotypes of Asthma.新兴哮喘表型的新疗法。
Annu Rev Med. 2020 Jan 27;71:289-302. doi: 10.1146/annurev-med-041818-020630. Epub 2019 Nov 5.
3
A T cell-myeloid IL-10 axis regulates pathogenic IFN-γ-dependent immunity in a mouse model of type 2-low asthma.
T 细胞-髓系细胞 IL-10 轴在 2 型低反应性哮喘小鼠模型中调节致病性 IFN-γ 依赖性免疫。
J Allergy Clin Immunol. 2020 Feb;145(2):666-678.e9. doi: 10.1016/j.jaci.2019.08.006. Epub 2019 Aug 22.
4
Opening the Window of Immune Opportunity: Treating Childhood Asthma.打开免疫机会之窗:治疗儿童哮喘。
Trends Immunol. 2019 Sep;40(9):786-798. doi: 10.1016/j.it.2019.07.004. Epub 2019 Aug 14.
5
The emergence of new biologics for severe asthma.新型生物制剂在重度哮喘中的应用。
Curr Opin Pharmacol. 2019 Jun;46:108-115. doi: 10.1016/j.coph.2019.05.005. Epub 2019 Jun 21.
6
Targeting the ICOS/ICOS-L pathway in a mouse model of established allergic asthma disrupts T follicular helper cell responses and ameliorates disease.在已建立的过敏性哮喘小鼠模型中靶向 ICOS/ICOS-L 途径会破坏 T 滤泡辅助细胞反应并改善疾病。
Allergy. 2019 Apr;74(4):650-662. doi: 10.1111/all.13602. Epub 2018 Nov 12.
7
Animal models of asthma: utility and limitations.哮喘的动物模型:效用与局限性
J Asthma Allergy. 2017 Nov 7;10:293-301. doi: 10.2147/JAA.S121092. eCollection 2017.
8
Gene Expression Correlated with Severe Asthma Characteristics Reveals Heterogeneous Mechanisms of Severe Disease.与重度哮喘特征相关的基因表达揭示了严重疾病的异质性机制。
Am J Respir Crit Care Med. 2017 Jun 1;195(11):1449-1463. doi: 10.1164/rccm.201607-1407OC.
9
Pulmonary ORMDL3 is critical for induction of Alternaria-induced allergic airways disease.肺部ORMDL3对于链格孢属诱导的过敏性气道疾病的诱导至关重要。
J Allergy Clin Immunol. 2017 May;139(5):1496-1507.e3. doi: 10.1016/j.jaci.2016.07.033. Epub 2016 Sep 10.
10
Current concepts of severe asthma.重度哮喘的当前概念
J Clin Invest. 2016 Jul 1;126(7):2394-403. doi: 10.1172/JCI84144.