Institute of Immunology, Friedrich-Loeffler-Institut, Federal Research Institute of Animal Health, Isle of Riems, Germany.
Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute of Animal Health, Isle of Riems, Germany.
Infect Immun. 2023 Feb 16;91(2):e0032322. doi: 10.1128/iai.00323-22. Epub 2023 Jan 23.
Dendritic cells (DCs) belong to the first line of innate defense and come into early contact with invading pathogens, including the zoonotic bacterium Coxiella burnetii, the causative agent of Q fever. However, the pathogen-host cell interactions in C. burnetii-infected DCs, particularly the role of mechanisms of immune subversion beyond virulent phase I lipopolysaccharide (LPS), as well as the contribution of cellular self-defense strategies, are not understood. Using phase II Coxiella-infected DCs, we show that impairment of DC maturation and MHC I downregulation is caused by autocrine release and action of immunosuppressive transforming growth factor-β (TGF-β). Our study demonstrates that IFN-γ reverses TGF-β impairment of maturation/MHC I presentation in infected DCs and activates bacterial elimination, predominantly by inducing iNOS/NO. Induced NO synthesis strongly affects bacterial growth and infectivity. Moreover, our studies hint that Coxiella-infected DCs might be able to protect themselves from mitotoxic NO by switching from oxidative phosphorylation to glycolysis, thus ensuring survival in self-defense against C. burnetii. Our results provide new insights into DC subversion by Coxiella and the IFN-γ-mediated targeting of C. burnetii during early steps in the innate immune response.
树突状细胞 (DCs) 属于先天防御的第一道防线,它们会与入侵病原体(包括引起 Q 热的动物源性细菌柯克斯体)早期接触。然而,柯克斯体感染的 DC 中病原体-宿主细胞的相互作用,特别是除了毒力相 I 脂多糖 (LPS) 以外的免疫抑制机制的作用,以及细胞自身防御策略的贡献,目前尚不清楚。我们使用相 II 柯克斯体感染的 DC 表明,自分泌释放和免疫抑制性转化生长因子-β (TGF-β) 的作用导致 DC 成熟和 MHC I 下调受损。我们的研究表明,IFN-γ 逆转了感染的 DC 中 TGF-β 对成熟/MHC I 呈递的损害,并通过诱导 iNOS/NO 激活细菌清除。诱导的 NO 合成强烈影响细菌的生长和感染力。此外,我们的研究表明,柯克斯体感染的 DC 可能能够通过从氧化磷酸化切换到糖酵解来保护自身免受细胞毒性 NO 的侵害,从而确保在针对柯克斯体的先天免疫反应早期自我防御中存活。我们的研究结果为柯克斯体对 DC 的抑制以及 IFN-γ 在先天免疫反应早期针对柯克斯体的靶向提供了新的见解。