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               <dc:title>Differential kinetics of splenic CD169+ macrophage death is one underlying cause of virus infection fate regulation</dc:title>
               <dc:creator>Casella, Valentina</dc:creator>
               <dc:creator>Domenjo-Vila, Eva</dc:creator>
               <dc:creator>Esteve-Codina, Anna</dc:creator>
               <dc:creator>Pedragosa, Mireia</dc:creator>
               <dc:creator>Cebollada Rica, Paula</dc:creator>
               <dc:creator>Vidal, Enric</dc:creator>
               <dc:creator>de la Rubia, Ivan</dc:creator>
               <dc:creator>López-Rodríguez, Cristina</dc:creator>
               <dc:creator>Bocharov, Gennady</dc:creator>
               <dc:creator>Argilaguet, Jordi</dc:creator>
               <dc:creator>Meyerhans, Andreas</dc:creator>
               <dc:contributor>Producció Animal</dc:contributor>
               <dc:contributor>Sanitat Animal</dc:contributor>
               <dc:description>Acute infection and chronic infection are the two most common fates of pathogenic virus infections. While several factors that&#xd;
contribute to these fates are described, the critical control points and the mechanisms that underlie infection fate regulation are&#xd;
incompletely understood. Using the acute and chronic lymphocytic choriomeningitis virus (LCMV) infection model of mice, we find&#xd;
that the early dynamic pattern of the IFN-I response is a differentiating trait between both infection fates. Acute-infected mice&#xd;
generate a 2-wave IFN-I response while chronic-infected mice generate only a 1-wave response. The underlying cause is a temporal&#xd;
difference in CD8 T cell-mediated killing of splenic marginal zone CD169+ macrophages. It occurs later in acute infection and thus&#xd;
enables CD169+ marginal zone macrophages to produce the 2nd IFN-I wave. This is required for subsequent immune events&#xd;
including induction of inflammatory macrophages, generation of effector CD8+ T cells and virus clearance. Importantly, these&#xd;
benefits come at a cost for the host in the form of spleen fibrosis. Due to an earlier marginal zone destruction, these ordered&#xd;
immune events are deregulated in chronic infection. Our findings demonstrate the critical importance of kinetically wellcoordinated sequential immune events for acute infection control and highlights that it may come at a cost for the host organism.</dc:description>
               <dc:date>2025-10-22T11:24:14Z</dc:date>
               <dc:date>2025-10-22T11:24:14Z</dc:date>
               <dc:date>2023-12-18</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:identifier>Casella, Valentina, Eva Domenjo-Vila, Anna Esteve‐Codina, Mireia Pedragosa, Paula Cebollada Rica, Enríc Vidal, Ivan De La Rubia, et al. 2023. “Differential Kinetics of Splenic CD169+ Macrophage Death Is One Underlying Cause of Virus Infection Fate Regulation.” Cell Death and Disease 14 (12): 838. doi:10.1038/s41419-023-06374-y.</dc:identifier>
               <dc:identifier>2041-4889</dc:identifier>
               <dc:identifier>http://hdl.handle.net/20.500.12327/2855</dc:identifier>
               <dc:identifier>https://doi.org/10.1038/s41419-023-06374-y</dc:identifier>
               <dc:language>eng</dc:language>
               <dc:relation>Cell Death and Disease</dc:relation>
               <dc:relation>MICIU/Programa Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I y Programa Estatal de I+D+I orientada a los retos de la sociedad/PID2019-106323RB-I00/ES/Characterization and manipulation of control points of virus infection fates/</dc:relation>
               <dc:relation>MICINN/Programa Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I/PID2022-141395OB-I00/ES/COORDINACION Y COOPERACION DE CELULAS INMUNES DURANTE INFECCIONES VIRALES AGUDAS Y CRONICAS/</dc:relation>
               <dc:relation>MICIU/Programa Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I/CEX2018-000792-M/ES/ /</dc:relation>
               <dc:relation>ISCIII/ /PT17-0009-0019/ES/ /</dc:relation>
               <dc:relation>FEDER/ / /EU/ /</dc:relation>
               <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:rights>Attribution 4.0 International</dc:rights>
               <dc:publisher>Springer Nature</dc:publisher>
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