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      <dc:title>Inborn Error of STAT2-Dependent IFN-I Immunity in a Patient Presented with Hemophagocytic Lymphohistiocytosis and Multisystem Inflammatory Syndrome in Children</dc:title>
      <dc:creator>López-Nevado, Marta</dc:creator>
      <dc:creator>Sevilla, Julián</dc:creator>
      <dc:creator>Almendro-Vázquez, Patricia</dc:creator>
      <dc:creator>Gil-Etayo, Francisco J.</dc:creator>
      <dc:creator>Garcinuño, Sara</dc:creator>
      <dc:creator>Serrano-Hernández, Antonio</dc:creator>
      <dc:creator>Paz Artal, Estela Natividad</dc:creator>
      <dc:creator>González Granado, Luis Ignacio</dc:creator>
      <dc:creator>Allende Martínez, Luis Miguel</dc:creator>
      <dc:description>Human inborn errors of immunity (IEI) affecting the type I interferon (IFN-I) induction pathway have been associated with predisposition to severe viral infections. Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening systemic hyperinflammatory syndrome that has been increasingly associated with inborn errors of IFN-I-mediated innate immunity. Here is reported a novel case of complete deficiency of STAT2 in a 3-year-old child that presented with typical features of HLH after mumps, measles, and rubella vaccination at the age of 12 months. Due to the life-threatening risk of viral infection, she received SARS-CoV-2 mRNA vaccination. Unfortunately, she developed multisystem inflammatory syndrome in children (MIS-C) after SARS-CoV-2 infection, 4 months after the last dose. Functional studies showed an impaired IFN-I-induced response and a defective IFNα expression at later stages of STAT2 pathway induction. These results suggest a possible more complex mechanism for hyperinflammatory reactions in this type of patients involving a possible defect in the IFN-I production. Understanding the cellular and molecular links between IFN-I-induced signaling and hyperinflammatory syndromes can be critical for the diagnosis and tailored management of these patients with predisposition to severe viral infection.</dc:description>
      <dc:date>2025-01-14T08:30:18Z</dc:date>
      <dc:date>2025-01-14T08:30:18Z</dc:date>
      <dc:date>2023-04-19</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>López-Nevado M, Sevilla J, Almendro-Vázquez P, Gil-Etayo FJ, Garcinuño S, Serrano-Hernández A, Paz-Artal E, González-Granado LI, Allende LM. Inborn Error of STAT2-Dependent IFN-I Immunity in a Patient Presented with Hemophagocytic Lymphohistiocytosis and Multisystem Inflammatory Syndrome in Children. J Clin Immunol. 2023 Aug;43(6):1278-1288. doi: 10.1007/s10875-023-01488-6. Epub 2023 Apr 19. PMID: 37074537; PMCID: PMC10113994.</dc:identifier>
      <dc:identifier>0271-9142</dc:identifier>
      <dc:identifier>1573-2592</dc:identifier>
      <dc:identifier>10.1007/s10875-023-01488-6</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/114117</dc:identifier>
      <dc:identifier>https://doi.org/10.1007/s10875-023-01488-6</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
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