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本文引用的文献

1
TGF-beta-exposed plasmacytoid dendritic cells participate in Th17 commitment.TGF-β 暴露的浆细胞样树突状细胞参与 Th17 细胞的分化。
J Immunol. 2011 Jun 1;186(11):6157-64. doi: 10.4049/jimmunol.1002497. Epub 2011 Apr 25.
2
Microbiota regulates immune defense against respiratory tract influenza A virus infection.微生物组调节免疫防御抵抗呼吸道流感 A 病毒感染。
Proc Natl Acad Sci U S A. 2011 Mar 29;108(13):5354-9. doi: 10.1073/pnas.1019378108. Epub 2011 Mar 14.
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CCR6 as a mediator of immunity in the lung and gut.CCR6 作为肺和肠道免疫的介质。
Exp Cell Res. 2011 Mar 10;317(5):613-9. doi: 10.1016/j.yexcr.2010.12.018.
4
Continuous expression of the transcription factor e2-2 maintains the cell fate of mature plasmacytoid dendritic cells.转录因子 e2-2 的持续表达维持了成熟浆细胞样树突状细胞的细胞命运。
Immunity. 2010 Dec 14;33(6):905-16. doi: 10.1016/j.immuni.2010.11.023. Epub 2010 Dec 9.
5
Tolerogenic plasmacytoid DC.耐受原浆细胞样树突状细胞。
Eur J Immunol. 2010 Oct;40(10):2667-76. doi: 10.1002/eji.201040839.
6
The expanding family of dendritic cell subsets.树突状细胞亚群不断扩大的家族。
Nat Biotechnol. 2010 Aug;28(8):813-5. doi: 10.1038/nbt0810-813.
7
Nonredundant role of CCRL2 in lung dendritic cell trafficking.CCRL2 在肺树突状细胞迁移中的非冗余作用。
Blood. 2010 Oct 21;116(16):2942-9. doi: 10.1182/blood-2009-12-259903. Epub 2010 Jul 6.
8
Paroxetine prevents loss of nigrostriatal dopaminergic neurons by inhibiting brain inflammation and oxidative stress in an experimental model of Parkinson's disease.帕罗西汀通过抑制帕金森病实验模型中的脑炎症和氧化应激来防止黑质纹状体多巴胺能神经元的丢失。
J Immunol. 2010 Jul 15;185(2):1230-7. doi: 10.4049/jimmunol.1000208. Epub 2010 Jun 21.
9
IgE regulates T helper cell differentiation through FcgammaRIII mediated dendritic cell cytokine modulation.IgE 通过 FcγRIII 介导的树突状细胞细胞因子调节来调节辅助性 T 细胞分化。
Cell Immunol. 2010;264(1):54-60. doi: 10.1016/j.cellimm.2010.04.011. Epub 2010 May 4.
10
The XC chemokine receptor 1 is a conserved selective marker of mammalian cells homologous to mouse CD8alpha+ dendritic cells.XC 趋化因子受体 1 是一种保守的选择性哺乳动物细胞标记物,与小鼠 CD8α+树突状细胞同源。
J Exp Med. 2010 Jun 7;207(6):1283-92. doi: 10.1084/jem.20100223. Epub 2010 May 17.

肺树突状细胞位于先天-适应性免疫界面。

Lung dendritic cells at the innate-adaptive immune interface.

机构信息

Department of Pediatrics, National Jewish Health, Denver, CO 80206, USA.

出版信息

J Leukoc Biol. 2011 Nov;90(5):883-95. doi: 10.1189/jlb.0311134. Epub 2011 Aug 1.

DOI:10.1189/jlb.0311134
PMID:21807741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3206474/
Abstract

This review updates the basic biology of lung DCs and their functions. Lung DCs have taken center stage as cellular therapeutic targets in new vaccine strategies for the treatment of diverse human disorders, including asthma, allergic lung inflammation, lung cancer, and infectious lung disease. The anatomical distribution of lung DCs, as well as the division of labor between their subsets, aids their ability to recognize and endocytose foreign substances and to process antigens. DCs can induce tolerance in or activate naïve T cells, making lung DCs well-suited to their role as lung sentinels. Lung DCs serve as a functional signaling/sensing unit to maintain lung homeostasis and orchestrate host responses to benign and harmful foreign substances.

摘要

这篇综述更新了肺树突状细胞的基础生物学及其功能。肺树突状细胞已成为新型疫苗策略中细胞治疗靶点,用于治疗多种人类疾病,包括哮喘、过敏性肺部炎症、肺癌和肺部传染病。肺树突状细胞的解剖分布以及它们亚群之间的分工,有助于它们识别和内吞外来物质和处理抗原。树突状细胞可以诱导或激活幼稚 T 细胞耐受,使肺树突状细胞非常适合作为肺部哨兵的角色。肺树突状细胞作为一个功能性信号/传感单位,维持肺内环境稳态,并协调宿主对良性和有害外来物质的反应。