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10.1007/s12016-020-08797-3

http://scihub22266oqcxt.onion/10.1007/s12016-020-08797-3
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32468411!8830198!32468411
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suck abstract from ncbi


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pmid32468411      Clin+Rev+Allergy+Immunol 2020 ; 59 (1): 78-88
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  • COVID-19 and Asthma: Reflection During the Pandemic #MMPMID32468411
  • Liu S; Zhi Y; Ying S
  • Clin Rev Allergy Immunol 2020[Aug]; 59 (1): 78-88 PMID32468411show ga
  • Coronavirus disease 2019 (COVID-19) is a global pandemic infectious disease caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), and abnormal, overactivated innate immunity and "cytokine storms" have been proposed as potential pathological mechanisms for rapid COVID-19 progression. Theoretically, asthmatic patients should have increased susceptibility and severity for SARS-CoV-2 infection due to a deficient antiviral immune response and the tendency for exacerbation elicited by common respiratory viruses. However, existing studies have not shown an expected prevalence of asthmatic individuals among COVID-19 patients. Certain aspects of type 2 immune response, including type 2 cytokines (IL-4, IL-13, etc.) and accumulation of eosinophils, might provide potential protective effects against COVID-19. Furthermore, conventional therapeutics for asthma, including inhaled corticosteroids, allergen immunotherapy (AIT), and anti-IgE monoclonal antibody, might also reduce the risks of asthmatics suffering infection of the virus through alleviating inflammation or enhancing antiviral defense. The interactions between COVID-19 and asthma deserve further attention and clarification.
  • |Administration, Inhalation[MESH]
  • |Adrenal Cortex Hormones/therapeutic use[MESH]
  • |Anti-Asthmatic Agents/therapeutic use[MESH]
  • |Asthma/*epidemiology/immunology/therapy[MESH]
  • |B-Lymphocytes/immunology[MESH]
  • |Betacoronavirus[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*epidemiology/immunology[MESH]
  • |Cytokines/immunology[MESH]
  • |Desensitization, Immunologic[MESH]
  • |Disease Progression[MESH]
  • |Eosinophils/immunology[MESH]
  • |Humans[MESH]
  • |Interleukin-13/immunology[MESH]
  • |Interleukin-4/immunology[MESH]
  • |Killer Cells, Natural/immunology[MESH]
  • |Lymphocytes/immunology[MESH]
  • |Macrophages/immunology[MESH]
  • |Natural Killer T-Cells/immunology[MESH]
  • |Omalizumab/therapeutic use[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*epidemiology/immunology[MESH]
  • |Protective Factors[MESH]
  • |Risk Factors[MESH]
  • |SARS-CoV-2[MESH]


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