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10.1684/ecn.2020.0453

http://scihub22266oqcxt.onion/10.1684/ecn.2020.0453
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33270024!ä!33270024

suck abstract from ncbi


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pmid33270024      Eur+Cytokine+Netw 2020 ; ä (ä): ä
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  • Therapeutic targeting of interleukin-6 for the treatment of COVID-19 #MMPMID33270024
  • Wang Y; Liu C; Miao X; Kong D; Zhao Y; Gong W; Ding X
  • Eur Cytokine Netw 2020[Dec]; ä (ä): ä PMID33270024show ga
  • Coronavirus disease 19 (COVID-19), caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first identified in China and has spread worldwide with a significant rate of infection. Considering the elevated levels of proinflammatory cytokines in COVID-19, it is suggested that cytokine storms play a critical role in its pathogenesis, including acute respiratory distress syndrome (ARDS). However, there is no specific drug for preventing the cytokine release syndrome (CRS) caused by COVID-19. Indeed, interleukin 6 (IL-6) has been highlighted for its many biological functions, such as immune regulation, inflammatory response, and metabolism. Therapeutic blockade of the IL-6 signaling pathway is expected to reduce the excessive immune reponse observed in COVID-19. Currently, the IL-6 receptor antagonists tocilizumab and sarilumab, have been adopted for preventing CRS during the progression of COVID-19, and remarkable beneficial effects were observed by using these humanized monoclonal antibodies. Based on the pathogenesis of COVID-19, we reviewed the biological mechanism of IL-6 blockade in the treatment of SARS-CoV-2 infection and evaluated its clinical applications.
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