Alexis M Duray, Leigh M Miller, Brooke P Dresden, Flavia Rago, Danielle Antos, Kevin J McHugh, John F Alcorn
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Additionally, Nrf2-/- mice had increased abundance of conventional type 1 dendritic cells (DCs). We then tested the interaction between DCs and T cells using an in vitro model of bone marrow-derived DCs with OVA and OT-II T cells. In this system, Nrf2-/- DCs promoted a Th2/regulatory T cell response as opposed to a Th1/Th17 response by WT DCs. This was recapitulated in vivo with superinfected Nrf2-/- mice having increased regulatory T cell populations. We also observed an increased median survival time of Nrf2-/- superinfected mice, due at least in part to increased IL-10 signaling, as anti-IL-10R Ab treatment reduced median survival time to levels seen in WT mice. Overall, these data suggest that loss of Nrf2 promotes differential T cell skewing mediated by DCs that promote a regulatory phenotype, increasing superinfection survival time, despite increased bacterial burden.</p>","PeriodicalId":16045,"journal":{"name":"Journal of immunology","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nrf2 Regulates Inflammation by Modulating Dendritic Cell-T Cell Crosstalk during Viral-Bacterial Superinfection.\",\"authors\":\"Alexis M Duray, Leigh M Miller, Brooke P Dresden, Flavia Rago, Danielle Antos, Kevin J McHugh, John F Alcorn\",\"doi\":\"10.4049/jimmunol.2400322\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Every year millions of people are infected with influenza, which can be complicated by secondary bacterial pneumonia. 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引用次数: 0
摘要
每年都有数百万人感染流感,并可能并发继发性细菌性肺炎。导致继发性细菌感染易感性增加的一个因素可能是炎症细胞因子的调节。NF 红细胞 2 相关因子 2(Nrf2)已被证明是抗氧化反应和各种炎症细胞因子的主调节因子。为了测试 Nrf2 在病毒-细菌超级感染过程中的作用,我们使用野生型(WT)或 Nrf2 缺失型(Nrf2-/-)小鼠建立了流感-金黄色葡萄球菌超级感染小鼠模型。在超级感染期间,Nrf2 的缺失降低了流感负荷,增加了金黄色葡萄球菌负荷。此外,Nrf2-/-小鼠的常规1型树突状细胞(DC)数量增加。然后,我们使用骨髓源性 DC 与 OVA 和 OT-II T 细胞的体外模型测试了 DC 与 T 细胞之间的相互作用。在这一系统中,Nrf2-/-DCs促进了Th2/调节性T细胞反应,而WT DCs则促进了Th1/Th17反应。这在体内得到了再现,超级感染的Nrf2-/-小鼠具有更多的调节性T细胞群。我们还观察到,Nrf2-/-超级感染小鼠的中位存活时间延长了,这至少部分归因于IL-10信号的增加,因为抗IL-10R Ab治疗使中位存活时间减少到了WT小鼠的水平。总之,这些数据表明,尽管细菌负荷增加,但Nrf2的缺失会促进由DC介导的不同T细胞倾斜,从而促进调节表型,延长超级感染存活时间。
Nrf2 Regulates Inflammation by Modulating Dendritic Cell-T Cell Crosstalk during Viral-Bacterial Superinfection.
Every year millions of people are infected with influenza, which can be complicated by secondary bacterial pneumonia. One factor that may contribute to increased susceptibility to secondary bacterial infection is the modulation of inflammatory cytokines. NF erythroid 2-related factor 2 (Nrf2) has been shown to be a master regulator of the antioxidant response and various inflammatory cytokines. To test the role of Nrf2 during viral-bacterial superinfection, we used a mouse model of influenza-Staphylococcus aureus superinfection with wild-type (WT) or Nrf2-deficient (Nrf2-/-) mice. Loss of Nrf2 reduced influenza burden and increased S. aureus burden during superinfection. Additionally, Nrf2-/- mice had increased abundance of conventional type 1 dendritic cells (DCs). We then tested the interaction between DCs and T cells using an in vitro model of bone marrow-derived DCs with OVA and OT-II T cells. In this system, Nrf2-/- DCs promoted a Th2/regulatory T cell response as opposed to a Th1/Th17 response by WT DCs. This was recapitulated in vivo with superinfected Nrf2-/- mice having increased regulatory T cell populations. We also observed an increased median survival time of Nrf2-/- superinfected mice, due at least in part to increased IL-10 signaling, as anti-IL-10R Ab treatment reduced median survival time to levels seen in WT mice. Overall, these data suggest that loss of Nrf2 promotes differential T cell skewing mediated by DCs that promote a regulatory phenotype, increasing superinfection survival time, despite increased bacterial burden.
期刊介绍:
The JI publishes novel, peer-reviewed findings in all areas of experimental immunology, including innate and adaptive immunity, inflammation, host defense, clinical immunology, autoimmunity and more. Special sections include Cutting Edge articles, Brief Reviews and Pillars of Immunology. The JI is published by The American Association of Immunologists (AAI)