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10.1016/j.ejphar.2022.175051

http://scihub22266oqcxt.onion/10.1016/j.ejphar.2022.175051
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35618037!9124632!35618037
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suck abstract from ncbi


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pmid35618037      Eur+J+Pharmacol 2022 ; 927 (ä): 175051
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  • Type-I interferons in the immunopathogenesis and treatment of Coronavirus disease 2019 #MMPMID35618037
  • Khorramdelazad H; Kazemi MH; Azimi M; Aghamajidi A; Mehrabadi AZ; Shahba F; Aghamohammadi N; Falak R; Faraji F; Jafari R
  • Eur J Pharmacol 2022[Jul]; 927 (ä): 175051 PMID35618037show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), is currently the major global health problem. Still, it continues to infect people globally and up to the end of February 2022, over 436 million confirmed cases of COVID-19, including 5.95 million deaths, were reported to the world health organization (WHO). No specific treatment is currently available for COVID-19, and the discovery of effective therapeutics requires understanding the effective immunologic and immunopathologic mechanisms behind this infection. Type-I interferons (IFN-Is), as the critical elements of the immediate immune response against viral infections, can inhibit the replication and spread of the viruses. However, the available evidence shows that the antiviral IFN-I response is impaired in patients with the severe form of COVID-19. Moreover, the administration of exogenous IFN-I in different phases of the disease can lead to various outcomes. Therefore, understanding the role of IFN-I molecules in COVID-19 development and its severity can provide valuable information for better management of this disease. This review summarizes the role of IFN-Is in the pathogenesis of COIVD-19 and discusses the importance of autoantibodies against this cytokine in the spreading of SARS-CoV-2 and control of the subsequent excessive inflammation.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Interferon Type I/therapeutic use[MESH]
  • |Cytokines[MESH]
  • |Humans[MESH]


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