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TGF-β/IFN-γ 拮抗作用在二期伯氏考克斯体感染树突状细胞中的颠覆和自卫。

TGF-β/IFN-γ Antagonism in Subversion and Self-Defense of Phase II Coxiella burnetiiInfected Dendritic Cells.

机构信息

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.

出版信息

Infect Immun. 2023 Feb 16;91(2):e0032322. doi: 10.1128/iai.00323-22. Epub 2023 Jan 23.

DOI:10.1128/iai.00323-22
PMID:36688662
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9933720/
Abstract

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.

摘要

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。