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10.1084/jem.20211818

http://scihub22266oqcxt.onion/10.1084/jem.20211818
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34757384!8590200!34757384
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suck abstract from ncbi


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pmid34757384      J+Exp+Med 2022 ; 219 (1): ä
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  • A stem-loop RNA RIG-I agonist protects against acute and chronic SARS-CoV-2 infection in mice #MMPMID34757384
  • Mao T; Israelow B; Lucas C; Vogels CBF; Gomez-Calvo ML; Fedorova O; Breban MI; Menasche BL; Dong H; Linehan M; Wilen CB; Landry ML; Grubaugh ND; Pyle AM; Iwasaki A
  • J Exp Med 2022[Jan]; 219 (1): ä PMID34757384show ga
  • As SARS-CoV-2 continues to cause morbidity and mortality around the world, there is an urgent need for the development of effective medical countermeasures. Here, we assessed the antiviral capacity of a minimal RIG-I agonist, stem-loop RNA 14 (SLR14), in viral control, disease prevention, post-infection therapy, and cross-variant protection in mouse models of SARS-CoV-2 infection. A single dose of SLR14 prevented viral infection in the lower respiratory tract and development of severe disease in a type I interferon (IFN-I)-dependent manner. SLR14 demonstrated remarkable prophylactic protective capacity against lethal SARS-CoV-2 infection and retained considerable efficacy as a therapeutic agent. In immunodeficient mice carrying chronic SARS-CoV-2 infection, SLR14 elicited near-sterilizing innate immunity in the absence of the adaptive immune system. In the context of infection with variants of concern (VOCs), SLR14 conferred broad protection against emerging VOCs. These findings demonstrate the therapeutic potential of SLR14 as a host-directed, broad-spectrum antiviral for early post-exposure treatment and treatment of chronically infected immunosuppressed patients.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |COVID-19/metabolism[MESH]
  • |Disease Models, Animal[MESH]
  • |Immunity, Innate/drug effects[MESH]
  • |Interferon Type I/metabolism[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]
  • |RNA/*metabolism[MESH]


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