
| 10.1016/j.chom.2020.07.005
http://scihub22266oqcxt.onion/10.1016/j.chom.2020.07.005
 32707096!7368656!32707096
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Cell+Host+Microbe 2020 ; 28 (3): 455-464.e2 Nephropedia Template TP
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Retrospective Multicenter Cohort Study Shows Early Interferon Therapy Is Associated with Favorable Clinical Responses in COVID-19 Patients #MMPMID32707096Wang N; Zhan Y; Zhu L; Hou Z; Liu F; Song P; Qiu F; Wang X; Zou X; Wan D; Qian X; Wang S; Guo Y; Yu H; Cui M; Tong G; Xu Y; Zheng Z; Lu Y; Hong PCell Host Microbe 2020[Sep]; 28 (3): 455-464.e2 PMID32707096show ga
Interferons (IFNs) are widely used in treating coronavirus disease 2019 (COVID-19) patients. However, a recent report of ACE2, the host factor mediating SARS-Cov-2 infection, identifying it as interferon-stimulated raised considerable safety concern. To examine the association between the use and timing of IFN-alpha2b and clinical outcomes, we analyzed in a retrospective multicenter cohort study of 446 COVID-19 patients in Hubei, China. Regression models estimated that early administration (|*Betacoronavirus[MESH]|Adolescent[MESH]|Adult[MESH]|Aged[MESH]|Aged, 80 and over[MESH]|Antiviral Agents/*administration & dosage/therapeutic use[MESH]|COVID-19[MESH]|COVID-19 Drug Treatment[MESH]|Child[MESH]|China/epidemiology[MESH]|Cohort Studies[MESH]|Coronavirus Infections/*drug therapy/epidemiology/mortality[MESH]|Drug Therapy, Combination[MESH]|Female[MESH]|Hospital Mortality[MESH]|Host Microbial Interactions/drug effects[MESH]|Humans[MESH]|Indoles/administration & dosage[MESH]|Interferon alpha-2[MESH]|Interferon-alpha/administration & dosage/*therapeutic use[MESH]|Length of Stay[MESH]|Lopinavir/administration & dosage[MESH]|Male[MESH]|Middle Aged[MESH]|Pandemics[MESH]|Pneumonia, Viral/*drug therapy/epidemiology/mortality[MESH]|Retrospective Studies[MESH]|Ritonavir/administration & dosage[MESH]|SARS-CoV-2[MESH]|Treatment Outcome[MESH]
  
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