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Exposure to Cigarette Smoke Inhibits the Pulmonary T-Cell Response to Influenza Virus and Mycobacterium tuberculosis

机译:暴露于香烟烟雾中可抑制肺部T细胞对流感病毒和结核分枝杆菌的反应

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摘要

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.
机译:吸烟与肺结核和流感的易感性增加有关。但是,关于这种易感性增加的机制的信息很少。小鼠不暴露或暴露于香烟中,然后通过气雾剂感染结核分枝杆菌或通过鼻内感染感染A型流感。一些小鼠接受了编码免疫原性结核分枝杆菌蛋白的DNA疫苗。测量了肺和脾中T细胞产生的γ-干扰素(IFN-γ)。在表达抗免疫分枝杆菌蛋白的构建体接种疫苗后,以及在体内感染结核分枝杆菌和甲型流感病毒期间,在用抗CD3进行体外刺激过程中,接触香烟烟雾抑制了肺T细胞产生IFN-γ。减少的IFN-γ产生是由积极调节IFN-γ表达的转录因子磷酸化程度降低介导的。接触香烟烟雾增加了感染结核分枝杆菌的小鼠的细菌负担,并增加了感染流感病毒的小鼠的体重减轻和死亡率。这项研究提供了第一个证明,即在生理相关的动物模型中,接触香烟烟雾直接抑制了肺部T细胞对结核分枝杆菌和流感病毒的反应,从而增加了对两种病原体的敏感性。

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