• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肺树突状细胞的发育与抗原摄取。

Pulmonary dendritic cell development and antigen acquisition.

机构信息

Integrated Department of Immunology, University of Colorado School of Medicine, Denver, CO, USA.

出版信息

Immunol Res. 2013 Mar;55(1-3):178-86. doi: 10.1007/s12026-012-8359-6.

DOI:10.1007/s12026-012-8359-6
PMID:22968708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4153344/
Abstract

Pulmonary dendritic cells (DCs) constantly sample the tissue and traffic inhaled antigens to the lung-draining lymph node where they normally orchestrate an appropriate immune response. The dynamic ability of these professional antigen-presenting cells to promote tolerance or immunity has been intensively studied by several groups, including ours. Distinct DC subsets in both lymphoid and non-lymphoid tissues have been described based on their surface molecule expression and location. Current efforts to unravel DC development and function are providing insight into the various roles each subset offers the immune system. Elucidating DC functions, particularly in the lung, may then allow use of the inherent ability of these cells for enhanced vaccine strategies and therapeutics for pulmonary infections and diseases.

摘要

肺树突状细胞(DCs)不断地对组织进行采样,并将吸入的抗原运送到肺引流淋巴结,在那里它们通常协调适当的免疫反应。这些专业抗原呈递细胞促进耐受或免疫的动态能力已经被包括我们在内的几个研究小组进行了深入研究。根据其表面分子表达和位置,已经描述了淋巴组织和非淋巴组织中的不同 DC 亚群。目前,人们正在努力揭示 DC 的发育和功能,这为了解每个亚群为免疫系统提供的各种作用提供了线索。阐明 DC 的功能,特别是在肺部,可能会使这些细胞的固有能力得到增强,从而用于肺部感染和疾病的疫苗策略和治疗。

相似文献

1
Pulmonary dendritic cell development and antigen acquisition.肺树突状细胞的发育与抗原摄取。
Immunol Res. 2013 Mar;55(1-3):178-86. doi: 10.1007/s12026-012-8359-6.
2
The antigen-presenting activities of Ia+ dendritic cells shift dynamically from lung to lymph node after an airway challenge with soluble antigen.在用可溶性抗原进行气道刺激后,Ia+树突状细胞的抗原呈递活性从肺动态转移至淋巴结。
J Exp Med. 1995 Apr 1;181(4):1275-83. doi: 10.1084/jem.181.4.1275.
3
Division of labor between dendritic cell subsets of the lung.肺中树突状细胞亚群之间的分工。
Mucosal Immunol. 2008 Nov;1(6):442-50. doi: 10.1038/mi.2008.39. Epub 2008 Sep 17.
4
No defect in T-cell priming, secondary response, or tolerance induction in response to inhaled antigens in Fms-like tyrosine kinase 3 ligand-deficient mice.在Fms样酪氨酸激酶3配体缺陷型小鼠中,对吸入抗原的T细胞启动、二次反应或耐受性诱导均无缺陷。
J Allergy Clin Immunol. 2005 Jan;115(1):192-9. doi: 10.1016/j.jaci.2004.08.046.
5
Intrinsic and cooperative antigen-presenting functions of dendritic-cell subsets in vivo.树突状细胞亚群在体内的固有和协同抗原呈递功能。
Nat Rev Immunol. 2007 Jul;7(7):543-55. doi: 10.1038/nri2103.
6
Efficient targeting of protein antigen to the dendritic cell receptor DEC-205 in the steady state leads to antigen presentation on major histocompatibility complex class I products and peripheral CD8+ T cell tolerance.在稳态下,将蛋白质抗原有效靶向树突状细胞受体DEC-205可导致抗原在主要组织相容性复合体I类产物上呈递,并诱导外周CD8+ T细胞产生耐受性。
J Exp Med. 2002 Dec 16;196(12):1627-38. doi: 10.1084/jem.20021598.
7
Respiratory syncytial virus-induced activation and migration of respiratory dendritic cells and subsequent antigen presentation in the lung-draining lymph node.呼吸道合胞病毒诱导呼吸道树突状细胞的激活与迁移以及随后在肺引流淋巴结中的抗原呈递。
J Virol. 2009 Jul;83(14):7235-43. doi: 10.1128/JVI.00452-09. Epub 2009 May 6.
8
CD103+ pulmonary dendritic cells preferentially acquire and present apoptotic cell-associated antigen.CD103+ 肺树突状细胞优先摄取和呈递凋亡细胞相关抗原。
J Exp Med. 2011 Aug 29;208(9):1789-97. doi: 10.1084/jem.20110538. Epub 2011 Aug 22.
9
Unique type I interferon responses determine the functional fate of migratory lung dendritic cells during influenza virus infection.独特的 I 型干扰素反应决定了流感病毒感染期间迁移性肺树突状细胞的功能命运。
PLoS Pathog. 2011 Nov;7(11):e1002345. doi: 10.1371/journal.ppat.1002345. Epub 2011 Nov 3.
10
Pulmonary response to inhaled antigen: neuroimmune interactions promote the recruitment of dendritic cells to the lung and the cellular immune response to inhaled antigen.肺部对吸入抗原的反应:神经免疫相互作用促进树突状细胞向肺部募集以及对吸入抗原的细胞免疫反应。
Am J Pathol. 1997 May;150(5):1735-43.

引用本文的文献

1
Nanoparticle-Based Pulmonary Immune Engineering.基于纳米颗粒的肺部免疫工程
Annu Rev Chem Biomol Eng. 2025 Jun;16(1):249-270. doi: 10.1146/annurev-chembioeng-082223-105117. Epub 2025 Mar 12.
2
Heat-Killed BBMN68 in Pasteurized Yogurt Alleviates Mugwort Pollen-Induced Allergic Airway Responses through Gut Microbiota Modulation in a Murine Model.巴氏杀菌酸奶中热灭活的BBMN68通过调节小鼠模型中的肠道微生物群减轻艾蒿花粉诱导的过敏性气道反应。
Foods. 2023 May 19;12(10):2049. doi: 10.3390/foods12102049.
3
Predicting the severity of COVID-19 patients using the CD24-CSF1R index in whole blood samples.使用全血样本中的CD24-CSF1R指数预测COVID-19患者的严重程度。
Heliyon. 2023 Mar;9(3):e13945. doi: 10.1016/j.heliyon.2023.e13945. Epub 2023 Feb 23.
4
Beyond allergic progression: From molecules to microbes as barrier modulators in the gut-lung axis functionality.超越过敏进展:从分子到微生物作为肠-肺轴功能中的屏障调节剂
Front Allergy. 2023 Jan 30;4:1093800. doi: 10.3389/falgy.2023.1093800. eCollection 2023.
5
Uncovering the core principles of the gut-lung axis to enhance innate immunity in the chicken.揭示肠-肺轴的核心原则,以增强鸡的先天免疫力。
Front Immunol. 2022 Oct 4;13:956670. doi: 10.3389/fimmu.2022.956670. eCollection 2022.
6
Lung fibroblasts facilitate pre-metastatic niche formation by remodeling the local immune microenvironment.肺成纤维细胞通过重塑局部免疫微环境促进转移前龛的形成。
Immunity. 2022 Aug 9;55(8):1483-1500.e9. doi: 10.1016/j.immuni.2022.07.001. Epub 2022 Jul 30.
7
HMGB1: A Potential Target of Nervus Vagus Stimulation in Pediatric SARS-CoV-2-Induced ALI/ARDS.高迁移率族蛋白B1:小儿严重急性呼吸综合征冠状病毒2诱导的急性肺损伤/急性呼吸窘迫综合征中迷走神经刺激的潜在靶点
Front Pediatr. 2022 May 11;10:884539. doi: 10.3389/fped.2022.884539. eCollection 2022.
8
[Pulmonary innate immune response in Sars-cov-2 infection].[新型冠状病毒2感染中的肺部固有免疫反应]
Rev Fac Cien Med Univ Nac Cordoba. 2022 Mar 7;79(1):33-42. doi: 10.31053/1853.0605.v79.n1.30642.
9
Lung dendritic cells migrate to the spleen to prime long-lived TCF1 memory CD8 T cell precursors after influenza infection.流感感染后,肺树突状细胞迁移到脾脏,为长寿命 TCF1 记忆 CD8 T 细胞前体提供启动信号。
Sci Immunol. 2021 Sep 10;6(63):eabg6895. doi: 10.1126/sciimmunol.abg6895.
10
Macrophage and Dendritic Cell Activation and Polarization in Response to Infection.巨噬细胞和树突状细胞对感染的激活与极化
J Fungi (Basel). 2021 Aug 3;7(8):630. doi: 10.3390/jof7080630.

本文引用的文献

1
Expression of the zinc finger transcription factor zDC (Zbtb46, Btbd4) defines the classical dendritic cell lineage.锌指转录因子 zDC(Zbtb46、Btbd4)的表达定义了经典的树突状细胞谱系。
J Exp Med. 2012 Jun 4;209(6):1153-65. doi: 10.1084/jem.20112675. Epub 2012 May 21.
2
Zbtb46 expression distinguishes classical dendritic cells and their committed progenitors from other immune lineages.Zbtb46 表达将经典树突状细胞及其定向祖细胞与其他免疫谱系区分开来。
J Exp Med. 2012 Jun 4;209(6):1135-52. doi: 10.1084/jem.20120030. Epub 2012 May 21.
3
Spatiotemporally separated antigen uptake by alveolar dendritic cells and airway presentation to T cells in the lung.肺泡树突状细胞时空分离抗原摄取和气道呈递至肺部 T 细胞。
J Exp Med. 2012 Jun 4;209(6):1183-99. doi: 10.1084/jem.20112667. Epub 2012 May 14.
4
Transcriptional programming of the dendritic cell network.树突状细胞网络的转录编程。
Nat Rev Immunol. 2012 Jan 25;12(2):101-13. doi: 10.1038/nri3149.
5
CD103+ pulmonary dendritic cells preferentially acquire and present apoptotic cell-associated antigen.CD103+ 肺树突状细胞优先摄取和呈递凋亡细胞相关抗原。
J Exp Med. 2011 Aug 29;208(9):1789-97. doi: 10.1084/jem.20110538. Epub 2011 Aug 22.
6
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.外显子组测序鉴定 GATA-2 突变是树突状细胞、单核细胞、B 和 NK 淋巴样细胞缺陷的原因。
Blood. 2011 Sep 8;118(10):2656-8. doi: 10.1182/blood-2011-06-360313. Epub 2011 Jul 15.
7
Id2 expression delineates differential checkpoints in the genetic program of CD8α+ and CD103+ dendritic cell lineages.Id2 表达描绘了 CD8α+ 和 CD103+ 树突状细胞谱系中遗传程序的不同检查点。
EMBO J. 2011 May 17;30(13):2690-704. doi: 10.1038/emboj.2011.163.
8
IRF8 mutations and human dendritic-cell immunodeficiency.IRF8 突变与人类树突状细胞免疫缺陷。
N Engl J Med. 2011 Jul 14;365(2):127-38. doi: 10.1056/NEJMoa1100066. Epub 2011 Apr 27.
9
Fas determines differential fates of resident and recruited macrophages during resolution of acute lung injury.Fas 决定了急性肺损伤消退过程中固有巨噬细胞和募集巨噬细胞的不同命运。
Am J Respir Crit Care Med. 2011 Sep 1;184(5):547-60. doi: 10.1164/rccm.201011-1891OC.
10
Cross-dressed dendritic cells drive memory CD8+ T-cell activation after viral infection.病毒感染后,异装树突状细胞驱动记忆性 CD8+T 细胞的激活。
Nature. 2011 Mar 31;471(7340):629-32. doi: 10.1038/nature09863.