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本文引用的文献

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J Allergy Clin Immunol. 2007 Jul;120(1):48-55. doi: 10.1016/j.jaci.2007.02.046. Epub 2007 May 7.
2
Mast cells are crucial for early inflammation, migration of Langerhans cells, and CTL responses following topical application of TLR7 ligand in mice.肥大细胞对于小鼠局部应用TLR7配体后的早期炎症、朗格汉斯细胞迁移及细胞毒性T淋巴细胞反应至关重要。
Blood. 2007 Aug 1;110(3):946-53. doi: 10.1182/blood-2006-07-036889. Epub 2007 Apr 19.
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Mast cells play a key role in the development of late airway hyperresponsiveness through TNF-alpha in a murine model of asthma.在哮喘小鼠模型中,肥大细胞通过肿瘤坏死因子-α在迟发性气道高反应性的发展中起关键作用。
Eur J Immunol. 2007 Apr;37(4):1107-15. doi: 10.1002/eji.200636612.
4
The effects of a monoclonal antibody directed against tumor necrosis factor-alpha in asthma.一种抗肿瘤坏死因子-α单克隆抗体在哮喘中的作用。
Am J Respir Crit Care Med. 2006 Oct 1;174(7):753-62. doi: 10.1164/rccm.200601-072OC. Epub 2006 Jul 13.
5
TNF-alpha is crucial for the development of mast cell-dependent colitis in mice.肿瘤坏死因子-α对于小鼠中肥大细胞依赖性结肠炎的发展至关重要。
Am J Physiol Gastrointest Liver Physiol. 2006 Nov;291(5):G969-76. doi: 10.1152/ajpgi.00146.2006. Epub 2006 Jun 22.
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Mast cells can promote the development of multiple features of chronic asthma in mice.肥大细胞可促进小鼠慢性哮喘多种特征的发展。
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The H1 histamine receptor regulates allergic lung responses.H1组胺受体调节肺部过敏反应。
J Clin Invest. 2006 Jun;116(6):1624-32. doi: 10.1172/JCI26150. Epub 2006 May 4.
8
The leukotriene B4 receptor (BLT1) is required for effector CD8+ T cell-mediated, mast cell-dependent airway hyperresponsiveness.白三烯B4受体(BLT1)是效应性CD8 + T细胞介导的、肥大细胞依赖性气道高反应性所必需的。
J Immunol. 2006 Mar 1;176(5):3157-64. doi: 10.4049/jimmunol.176.5.3157.
9
Evidence of a role of tumor necrosis factor alpha in refractory asthma.肿瘤坏死因子α在难治性哮喘中作用的证据。
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Regulation of allergic airway inflammation through Toll-like receptor 4-mediated modification of mast cell function.通过Toll样受体4介导的肥大细胞功能修饰调控过敏性气道炎症
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肥大细胞与过敏性气道疾病的发生发展。

Mast cells and the development of allergic airway disease.

机构信息

III, Medical Clinic, Dept, of Pulmonary Medicine, Johannes-Gutenberg-University, Langenbeckstr, 1, 55101 Mainz, Germany.

出版信息

J Occup Med Toxicol. 2008 Feb 27;3 Suppl 1(Suppl 1):S2. doi: 10.1186/1745-6673-3-S1-S2.

DOI:10.1186/1745-6673-3-S1-S2
PMID:18315833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2259396/
Abstract

Murine models have highlighted the importance of T-cells and TH2 cytokines in development of allergen-induced airway disease. In contrast, the role of mast cells for the development of allergic airway disease has been controversial. Recent studies in murine models demonstrate a significant contribution of mast cells during the development of airway hyperresponsiveness and airway inflammation. Furthermore these models have allowed identifying certain mast cell-produced mediators (e.g. histamine and leukotriene B4) to be involved in the recruitment of effector T-cells into the lung. Additionally, mast cell-produced TNF can directly activate TH2 cells and contribute to the development of allergic airway disease. These new findings demonstrate a complex role of mast cells and their mediators, not only as effector cells, but also during sensitization and development of allergic airway disease. Therefore mast cells and certain mast cell-produced mediators might be an interesting target for the prevention and treatment of allergic asthma.

摘要

鼠类模型突出了 T 细胞和 TH2 细胞因子在变应原诱导的气道疾病发展中的重要性。相比之下,肥大细胞在过敏性气道疾病发展中的作用一直存在争议。最近的鼠类模型研究表明,肥大细胞在气道高反应性和气道炎症的发展过程中具有重要作用。此外,这些模型还确定了某些肥大细胞产生的介质(例如组胺和白三烯 B4)参与效应 T 细胞向肺部的募集。此外,肥大细胞产生的 TNF 可以直接激活 TH2 细胞,并有助于过敏性气道疾病的发展。这些新发现表明肥大细胞及其介质不仅作为效应细胞,而且在致敏和过敏性气道疾病发展过程中具有复杂的作用。因此,肥大细胞和某些肥大细胞产生的介质可能是预防和治疗过敏性哮喘的一个有趣的靶点。