<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Matthiesen S</submitter><funding>Bundesministerium für Bildung und Forschung</funding><pagination>e0032322</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9933720</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>91(2)</volume><pubmed_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.</pubmed_abstract><journal>Infection and immunity</journal><pubmed_title>TGF-β/IFN-γ Antagonism in Subversion and Self-Defense of Phase II Coxiella burnetii&lt;i>-&lt;/i>Infected Dendritic Cells.</pubmed_title><pmcid>PMC9933720</pmcid><funding_grant_id>01KI1726C</funding_grant_id><pubmed_authors>Karger A</pubmed_authors><pubmed_authors>Franzke K</pubmed_authors><pubmed_authors>Jahnke R</pubmed_authors><pubmed_authors>Christiansen B</pubmed_authors><pubmed_authors>Zaeck LM</pubmed_authors><pubmed_authors>Knittler MR</pubmed_authors><pubmed_authors>Matthiesen S</pubmed_authors><pubmed_authors>Finke S</pubmed_authors></additional><is_claimable>false</is_claimable><name>TGF-β/IFN-γ Antagonism in Subversion and Self-Defense of Phase II Coxiella burnetii&lt;i>-&lt;/i>Infected Dendritic Cells.</name><description>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.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-06-08T06:41:28.609Z</modification><creation>2024-12-04T07:36:00.369Z</creation></dates><accession>S-EPMC9933720</accession><cross_references><pubmed>36688662</pubmed><doi>10.1128/iai.00323-22</doi></cross_references></HashMap>