• 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

相似文献

1
Roles of Mucosal Immunity against Mycobacterium tuberculosis Infection.黏膜免疫在抗结核分枝杆菌感染中的作用。
Tuberc Res Treat. 2012;2012:791728. doi: 10.1155/2012/791728. Epub 2012 Nov 1.
2
Tuberculosis结核病
3
[Development of antituberculous drugs: current status and future prospects].[抗结核药物的研发:现状与未来前景]
Kekkaku. 2006 Dec;81(12):753-74.
4
Functional Signatures of Human CD4 and CD8 T Cell Responses to Mycobacterium tuberculosis.人类CD4和CD8 T细胞对结核分枝杆菌反应的功能特征
Front Immunol. 2014 Apr 22;5:180. doi: 10.3389/fimmu.2014.00180. eCollection 2014.
5
Natural and trained innate immunity against Mycobacterium tuberculosis.天然和训练有素的固有免疫对抗结核分枝杆菌。
Immunobiology. 2020 May;225(3):151951. doi: 10.1016/j.imbio.2020.151951. Epub 2020 Apr 27.
6
Novel lipopeptides of ESAT-6 induce strong protective immunity against Mycobacterium tuberculosis: Routes of immunization and TLR agonists critically impact vaccine's efficacy.新型ESAT-6脂肽诱导针对结核分枝杆菌的强大保护性免疫:免疫途径和TLR激动剂对疫苗效力有至关重要的影响。
Vaccine. 2016 Nov 4;34(46):5677-5688. doi: 10.1016/j.vaccine.2016.08.075. Epub 2016 Sep 29.
7
[Frontier of mycobacterium research--host vs. mycobacterium].[分枝杆菌研究前沿——宿主与分枝杆菌]
Kekkaku. 2005 Sep;80(9):613-29.
8
miRNAs in immune responses to Mycobacterium tuberculosis infection.miRNAs 在结核分枝杆菌感染的免疫反应中的作用。
Cancer Lett. 2018 Sep 1;431:22-30. doi: 10.1016/j.canlet.2018.05.028. Epub 2018 May 25.
9
Unexpected role for IL-17 in protective immunity against hypervirulent Mycobacterium tuberculosis HN878 infection.白细胞介素-17在抗高毒力结核分枝杆菌HN878感染的保护性免疫中的意外作用。
PLoS Pathog. 2014 May 15;10(5):e1004099. doi: 10.1371/journal.ppat.1004099. eCollection 2014 May.
10
Cell-Mediated Immune Responses to -Expressed and Stage-Specific Antigens in Latent and Active Tuberculosis Across Different Age Groups.细胞介导的免疫反应对潜伏和活动性结核病中表达和阶段特异性抗原的反应在不同年龄组中。
Front Immunol. 2020 Feb 11;11:103. doi: 10.3389/fimmu.2020.00103. eCollection 2020.

引用本文的文献

1
The Role and Potential Application of IL-12 in the Immune Regulation of Tuberculosis.白细胞介素-12在结核病免疫调节中的作用及潜在应用
Int J Mol Sci. 2025 Mar 28;26(7):3106. doi: 10.3390/ijms26073106.
2
Editorial: Tuberculosis and humoral immunity.社论:结核病与体液免疫
Front Immunol. 2025 Feb 10;16:1562567. doi: 10.3389/fimmu.2025.1562567. eCollection 2025.
3
Strong immune responses and robust protection following a novel protein in adjuvant tuberculosis vaccine candidate.新型含佐剂结核疫苗候选蛋白诱导强烈免疫反应及有效保护。
Sci Rep. 2025 Jan 13;15(1):1886. doi: 10.1038/s41598-024-84667-8.
4
Clarification of a unique mucosal vaccination route for improved systemic and mucosal immune response in broiler.明确一种独特的黏膜疫苗接种途径以改善肉鸡的全身和黏膜免疫反应。
Heliyon. 2024 Oct 19;10(20):e39621. doi: 10.1016/j.heliyon.2024.e39621. eCollection 2024 Oct 30.
5
Next-Generation TB Vaccines: Progress, Challenges, and Prospects.下一代结核病疫苗:进展、挑战与前景
Vaccines (Basel). 2023 Jul 31;11(8):1304. doi: 10.3390/vaccines11081304.
6
Target Identification in Anti-Tuberculosis Drug Discovery.抗结核药物发现中的靶点鉴定。
Int J Mol Sci. 2023 Jun 22;24(13):10482. doi: 10.3390/ijms241310482.
7
Generating enhanced mucosal immunity against current challenges and new directions.生成针对当前挑战和新方向的增强黏膜免疫。
Front Immunol. 2023 Feb 21;14:1126107. doi: 10.3389/fimmu.2023.1126107. eCollection 2023.
8
Mucosal exposure to non-tuberculous mycobacteria elicits B cell-mediated immunity against pulmonary tuberculosis.黏膜接触非结核分枝杆菌会引发针对肺结核的 B 细胞介导免疫。
Cell Rep. 2022 Dec 13;41(11):111783. doi: 10.1016/j.celrep.2022.111783.
9
BCG vaccination strategies against tuberculosis: updates and perspectives.BCG 疫苗接种策略防治结核病:更新与展望。
Hum Vaccin Immunother. 2021 Dec 2;17(12):5284-5295. doi: 10.1080/21645515.2021.2007711.
10
Characterization of local and circulating bovine γδ T cell responses to respiratory BCG vaccination.鉴定局部和循环牛γδ T 细胞对呼吸卡介苗接种的反应。
Sci Rep. 2019 Nov 5;9(1):15996. doi: 10.1038/s41598-019-52565-z.

本文引用的文献

1
The role of airway epithelial cells in response to mycobacteria infection.气道上皮细胞在应对分枝杆菌感染中的作用。
Clin Dev Immunol. 2012;2012:791392. doi: 10.1155/2012/791392. Epub 2012 Apr 18.
2
The CFP10/ESAT6 complex of Mycobacterium tuberculosis may function as a regulator of macrophage cell death at different stages of tuberculosis infection.结核分枝杆菌的 CFP10/ESAT6 复合物可能在结核病感染的不同阶段作为调节巨噬细胞细胞死亡的因子发挥作用。
Med Hypotheses. 2012 Mar;78(3):389-92. doi: 10.1016/j.mehy.2011.11.022. Epub 2011 Dec 21.
3
Pathogenesis in tuberculosis: transcriptomic approaches to unraveling virulence mechanisms and finding new drug targets.结核病发病机制:转录组学方法揭示毒力机制和寻找新的药物靶点。
FEMS Microbiol Rev. 2012 Mar;36(2):463-85. doi: 10.1111/j.1574-6976.2011.00302.x. Epub 2011 Sep 15.
4
Increased IL-17A expression in granulomas and in circulating memory T cells in sarcoidosis.结节病患者肉芽肿和循环记忆 T 细胞中白细胞介素-17A 的表达增加。
Rheumatology (Oxford). 2012 Jan;51(1):37-46. doi: 10.1093/rheumatology/ker316. Epub 2011 Nov 10.
5
Mycobacterium tuberculosis infection induces non-apoptotic cell death of human dendritic cells.结核分枝杆菌感染诱导人树突状细胞发生非凋亡性细胞死亡。
BMC Microbiol. 2011 Oct 24;11:237. doi: 10.1186/1471-2180-11-237.
6
Cellular immune responses to nine Mycobacterium tuberculosis vaccine candidates following intranasal vaccination.经鼻腔接种后九种结核分枝杆菌候选疫苗的细胞免疫应答。
PLoS One. 2011;6(7):e22718. doi: 10.1371/journal.pone.0022718. Epub 2011 Jul 25.
7
Nanoparticle conjugation and pulmonary delivery enhance the protective efficacy of Ag85B and CpG against tuberculosis.纳米颗粒缀合和肺部递药增强 Ag85B 和 CpG 对结核病的保护效力。
Vaccine. 2011 Sep 16;29(40):6959-66. doi: 10.1016/j.vaccine.2011.07.039. Epub 2011 Jul 23.
8
Mycobacterium tuberculosislpdC, Rv0462, induces dendritic cell maturation and Th1 polarization.结核分枝杆菌 lpdC(Mycobacterium tuberculosislpdC, Rv0462)诱导树突状细胞成熟和 Th1 极化。
Biochem Biophys Res Commun. 2011 Aug 5;411(3):642-7. doi: 10.1016/j.bbrc.2011.07.013. Epub 2011 Jul 18.
9
Dendritic Cells Activate and Mature after Infection with Mycobacterium tuberculosis.结核分枝杆菌感染后,树突状细胞被激活并成熟。
BMC Res Notes. 2011 Jul 21;4:247. doi: 10.1186/1756-0500-4-247.
10
Effects of Mycobacterium tuberculosis ESAT-6/CFP-10 fusion protein on the autophagy function of mouse macrophages.结核分枝杆菌 ESAT-6/CFP-10 融合蛋白对小鼠巨噬细胞自噬功能的影响。
DNA Cell Biol. 2012 Feb;31(2):171-9. doi: 10.1089/dna.2011.1290. Epub 2011 Jul 8.

黏膜免疫在抗结核分枝杆菌感染中的作用。

Roles of Mucosal Immunity against Mycobacterium tuberculosis Infection.

作者信息

Li Wu, Deng Guangcun, Li Min, Liu Xiaoming, Wang Yujiong

机构信息

Key Laboratory of Ministry of Education for Conservation and Utilization of Special Biological Resources in the Western, Ningxia University, Yinchuan, Ningxia 750021, China ; College of Life Science, Ningxia University, 539 W. Helanshan Road, Xixia District, Yinchuan, Ningxia 750021, China.

出版信息

Tuberc Res Treat. 2012;2012:791728. doi: 10.1155/2012/791728. Epub 2012 Nov 1.

DOI:10.1155/2012/791728
PMID:23213508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3504404/
Abstract

Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), is one of the world's leading infectious causes of morbidity and mortality. As a mucosal-transmitted pathogen, Mtb infects humans and animals mainly through the mucosal tissue of the respiratory tract. Apart from providing a physical barrier against the invasion of pathogen, the major function of the respiratory mucosa may be to serve as the inductive sites to initiate mucosal immune responses and sequentially provide the first line of defense for the host to defend against this pathogen. A large body of studies in the animals and humans have demonstrated that the mucosal immune system, rather than the systemic immune system, plays fundamental roles in the host's defense against Mtb infection. Therefore, the development of new vaccines and novel delivery routes capable of directly inducing respiratory mucosal immunity is emphasized for achieving enhanced protection from Mtb infection. In this paper, we outline the current state of knowledge regarding the mucosal immunity against Mtb infection, including the development of TB vaccines, and respiratory delivery routes to enhance mucosal immunity are discussed.

摘要

结核分枝杆菌(Mtb)是结核病(TB)的病原体,是全球导致发病和死亡的主要感染原因之一。作为一种通过黏膜传播的病原体,Mtb主要通过呼吸道的黏膜组织感染人类和动物。除了提供抵御病原体入侵的物理屏障外,呼吸道黏膜的主要功能可能是作为启动黏膜免疫反应的诱导部位,并依次为宿主抵御这种病原体提供第一道防线。大量在动物和人类中的研究表明,黏膜免疫系统而非全身免疫系统在宿主抵御Mtb感染中发挥着基础性作用。因此,强调开发能够直接诱导呼吸道黏膜免疫的新型疫苗和新型给药途径,以实现增强对Mtb感染的保护。在本文中,我们概述了关于针对Mtb感染的黏膜免疫的当前知识状态,包括结核病疫苗的发展,并讨论了增强黏膜免疫的呼吸道给药途径。