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10.1016/j.jinf.2020.07.016

http://scihub22266oqcxt.onion/10.1016/j.jinf.2020.07.016
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suck abstract from ncbi


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pmid32707230      J+Infect 2020 ; 81 (4): e1-e10
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  • Differential immune activation profile of SARS-CoV-2 and SARS-CoV infection in human lung and intestinal cells: Implications for treatment with IFN-beta and IFN inducer #MMPMID32707230
  • Shuai H; Chu H; Hou Y; Yang D; Wang Y; Hu B; Huang X; Zhang X; Chai Y; Cai JP; Chan JF; Yuen KY
  • J Infect 2020[Oct]; 81 (4): e1-e10 PMID32707230show ga
  • OBJECTIVES: Respiratory and intestinal tract are two primary target organs of SARS-CoV-2 infection. However, detailed characterization of the host-virus interplay in infected human lung and intestinal epithelial cells is lacking. METHODS: We utilized immunofluorescence assays, flow cytometry, and RT-qPCR to delineate the virological features and the innate immune response of the host cells against SARS-CoV-2 infection in two prototype human cell lines representing the human lung (Calu3) and intestinal (Caco2) epithelium when compared with SARS-CoV. RESULTS: Lung epithelial cells were significantly more susceptible to SARS-CoV-2 compared to SARS-CoV. However, SARS-CoV-2 infection induced an attenuated pro-inflammatory cytokines/chemokines induction and type I and type II IFN responses. A single dose of 10?U/mL interferon-beta (IFNbeta) pretreatment potently protected both Calu3 and Caco2 against SARS-CoV-2 infection. Interestingly, SARS-CoV-2 was more sensitive to the pretreatment with IFNbeta and IFN inducer than SARS-CoV in Calu3. CONCLUSIONS: Despite robust infection in both human lung and intestinal epithelial cells, SARS-CoV-2 could attenuate the virus-induced pro-inflammatory response and IFN response. Pre-activation of the type I IFN signaling pathway primed a highly efficient antiviral response in the host against SARS-CoV-2 infection, which could serve as a potential therapeutic and prophylactic maneuver to COVID-19 patients.
  • |Antiviral Agents/pharmacology[MESH]
  • |Betacoronavirus/immunology[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Caco-2 Cells[MESH]
  • |Cell Line, Tumor[MESH]
  • |Coronavirus Infections/drug therapy/*immunology[MESH]
  • |Epithelial Cells/virology[MESH]
  • |Humans[MESH]
  • |Immunity, Innate[MESH]
  • |Interferon Inducers/*pharmacology[MESH]
  • |Interferon-beta/*pharmacology[MESH]
  • |Intestinal Mucosa/*immunology[MESH]
  • |Lung/immunology[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*immunology[MESH]
  • |Respiratory Mucosa/*immunology[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*immunology[MESH]


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