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Chronic cigarette smoke exposure primes NK cell activation in a mouse model of chronic obstructive pulmonary disease.慢性香烟烟雾暴露使慢性阻塞性肺疾病小鼠模型中的自然杀伤细胞活化。
J Immunol. 2010 Apr 15;184(8):4460-9. doi: 10.4049/jimmunol.0903654. Epub 2010 Mar 12.
2
Secondhand smoke and infectious disease in adults: A global women's health concern: Comment on "Passive Smoking and Tuberculosis".成人中的二手烟与传染病:一项全球女性健康问题:评《被动吸烟与结核病》
Arch Intern Med. 2010 Feb 8;170(3):292-3. doi: 10.1001/archinternmed.2009.501.
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Immunity to avian influenza A viruses.对甲型禽流感病毒的免疫力。
Rev Sci Tech. 2009 Apr;28(1):175-85. doi: 10.20506/rst.28.1.1857.
4
Association between tobacco smoking and active tuberculosis in Taiwan: prospective cohort study.台湾地区吸烟与活动性肺结核之间的关联:前瞻性队列研究。
Am J Respir Crit Care Med. 2009 Sep 1;180(5):475-80. doi: 10.1164/rccm.200904-0549OC. Epub 2009 Jun 19.
5
Vaccination strategies to enhance local immunity and protection against Mycobacteriun tuberculosis.增强局部免疫力及预防结核分枝杆菌感染的疫苗接种策略。
Vaccine. 2009 Mar 13;27(12):1816-24. doi: 10.1016/j.vaccine.2009.01.119.
6
The 1918 "Spanish flu" in Spain.1918年西班牙的“西班牙流感”。
Clin Infect Dis. 2008 Sep 1;47(5):668-73. doi: 10.1086/590567.
7
CREB, ATF, and AP-1 transcription factors regulate IFN-gamma secretion by human T cells in response to mycobacterial antigen.CREB、ATF和AP-1转录因子通过人类T细胞响应分枝杆菌抗原调节γ-干扰素的分泌。
J Immunol. 2008 Aug 1;181(3):2056-64. doi: 10.4049/jimmunol.181.3.2056.
8
Cigarette smoke worsens lung inflammation and impairs resolution of influenza infection in mice.香烟烟雾会加重小鼠的肺部炎症,并损害流感感染的消退。
Respir Res. 2008 Jul 15;9(1):53. doi: 10.1186/1465-9921-9-53.
9
Cigarette smoke-induced oxidative stress suppresses generation of dendritic cell IL-12 and IL-23 through ERK-dependent pathways.香烟烟雾诱导的氧化应激通过ERK依赖途径抑制树突状细胞IL-12和IL-23的产生。
J Immunol. 2008 Jul 15;181(2):1536-47. doi: 10.4049/jimmunol.181.2.1536.
10
High-dose but not low-dose mainstream cigarette smoke suppresses allergic airway inflammation by inhibiting T cell function.高剂量而非低剂量的主流香烟烟雾通过抑制T细胞功能来抑制过敏性气道炎症。
Am J Physiol Lung Cell Mol Physiol. 2008 Sep;295(3):L412-21. doi: 10.1152/ajplung.00392.2007. Epub 2008 Jun 20.

暴露于香烟烟雾会抑制肺部对流感病毒和结核分枝杆菌的 T 细胞反应。

Exposure to cigarette smoke inhibits the pulmonary T-cell response to influenza virus and Mycobacterium tuberculosis.

机构信息

Center for Pulmonary and Infectious Disease Control, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, USA.

出版信息

Infect Immun. 2011 Jan;79(1):229-37. doi: 10.1128/IAI.00709-10. Epub 2010 Oct 25.

DOI:10.1128/IAI.00709-10
PMID:20974820
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3019896/
Abstract

Smoking is associated with increased susceptibility to tuberculosis and influenza. However, little information is available on the mechanisms underlying this increased susceptibility. Mice were left unexposed or were exposed to cigarette smoke and then infected with Mycobacterium tuberculosis by aerosol or influenza A by intranasal infection. Some mice were given a DNA vaccine encoding an immunogenic M. tuberculosis protein. Gamma interferon (IFN-γ) production by T cells from the lungs and spleens was measured. Cigarette smoke exposure inhibited the lung T-cell production of IFN-γ during stimulation in vitro with anti-CD3, after vaccination with a construct expressing an immunogenic mycobacterial protein, and during infection with M. tuberculosis and influenza A virus in vivo. Reduced IFN-γ production was mediated through the decreased phosphorylation of transcription factors that positively regulate IFN-γ expression. Cigarette smoke exposure increased the bacterial burden in mice infected with M. tuberculosis and increased weight loss and mortality in mice infected with influenza virus. This study provides the first demonstration that cigarette smoke exposure directly inhibits the pulmonary T-cell response to M. tuberculosis and influenza virus in a physiologically relevant animal model, increasing susceptibility to both pathogens.

摘要

吸烟会增加感染结核病和流感的易感性。然而,目前对于这种易感性增加的机制知之甚少。将小鼠暴露于或不暴露于香烟烟雾中,然后通过气溶胶感染结核分枝杆菌或通过鼻腔感染流感 A 病毒。一些小鼠给予编码免疫原性结核分枝杆菌蛋白的 DNA 疫苗。测量来自肺部和脾脏的 T 细胞产生的γ干扰素(IFN-γ)。在体外用抗 CD3 刺激、用表达免疫原性分枝杆菌蛋白的构建物接种疫苗以及在体内感染结核分枝杆菌和流感 A 病毒期间,香烟烟雾暴露抑制了肺 T 细胞产生 IFN-γ。IFN-γ 产生减少是通过正调节 IFN-γ 表达的转录因子的磷酸化减少介导的。香烟烟雾暴露增加了感染结核分枝杆菌的小鼠的细菌负荷,并增加了感染流感病毒的小鼠的体重减轻和死亡率。这项研究首次证明,香烟烟雾暴露直接抑制生理相关动物模型中肺 T 细胞对结核分枝杆菌和流感病毒的反应,增加了对这两种病原体的易感性。