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10.3389/fimmu.2020.01708

http://scihub22266oqcxt.onion/10.3389/fimmu.2020.01708
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32754163!7365923!32754163
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suck abstract from ncbi


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pmid32754163      Front+Immunol 2020 ; 11 (ä): 1708
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  • Cytokine Storm in COVID-19: The Current Evidence and Treatment Strategies #MMPMID32754163
  • Tang Y; Liu J; Zhang D; Xu Z; Ji J; Wen C
  • Front Immunol 2020[]; 11 (ä): 1708 PMID32754163show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) is the pathogen that causes coronavirus disease 2019 (COVID-19). As of 25 May 2020, the outbreak of COVID-19 has caused 347,192 deaths around the world. The current evidence showed that severely ill patients tend to have a high concentration of pro-inflammatory cytokines, such as interleukin (IL)-6, compared to those who are moderately ill. The high level of cytokines also indicates a poor prognosis in COVID-19. Besides, excessive infiltration of pro-inflammatory cells, mainly involving macrophages and T-helper 17 cells, has been found in lung tissues of patients with COVID-19 by postmortem examination. Recently, increasing studies indicate that the "cytokine storm" may contribute to the mortality of COVID-19. Here, we summarize the clinical and pathologic features of the cytokine storm in COVID-19. Our review shows that SARS-Cov-2 selectively induces a high level of IL-6 and results in the exhaustion of lymphocytes. The current evidence indicates that tocilizumab, an IL-6 inhibitor, is relatively effective and safe. Besides, corticosteroids, programmed cell death protein (PD)-1/PD-L1 checkpoint inhibition, cytokine-adsorption devices, intravenous immunoglobulin, and antimalarial agents could be potentially useful and reliable approaches to counteract cytokine storm in COVID-19 patients.
  • |Adrenal Cortex Hormones/therapeutic use[MESH]
  • |Animals[MESH]
  • |Antibodies, Monoclonal, Humanized/pharmacology/therapeutic use[MESH]
  • |Antimalarials/therapeutic use[MESH]
  • |Artesunate/therapeutic use[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*drug therapy/*immunology/virology[MESH]
  • |Hemoperfusion/methods[MESH]
  • |Humans[MESH]
  • |Hydroxychloroquine/therapeutic use[MESH]
  • |Immunoglobulins, Intravenous/therapeutic use[MESH]
  • |Interleukin-6/antagonists & inhibitors/*metabolism[MESH]
  • |Mice[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/*immunology/virology[MESH]
  • |Programmed Cell Death 1 Receptor/antagonists & inhibitors[MESH]


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