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10.1016/j.gene.2021.145574

http://scihub22266oqcxt.onion/10.1016/j.gene.2021.145574
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suck abstract from ncbi


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pmid33737124      Gene 2021 ; 783 (ä): 145574
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  • Epidemiological transcriptomic data supports BCG protection in viral diseases including COVID-19 #MMPMID33737124
  • Sharma A
  • Gene 2021[May]; 783 (ä): 145574 PMID33737124show ga
  • Epidemiological and clinical evidence suggests that Bacille Calmette-Guerin (BCG) vaccine induced trained immunity protects against non-specific infections. Multiple clinical trials are currently underway to assess effectiveness of the vaccine in the coronavirus disease 2019 (COVID-19). However, the durability and mechanism of BCG trained immunity remain unclear. Here, an integrative analysis of available epidemiological transcriptomic data related to BCG vaccination and respiratory tract viral infections as well as of reported transcriptomic alterations in COVID-19 is presented toward addressing this gap. Results suggest that the vaccine induces very long-lasting transcriptomic changes that mimic viral infections by, consistent with the present concept of trained immunity, upregulation of antiviral defense response, and oppose viral infections by, inconsistent with the concept, downregulation of myeloid cell activation. These durability and mechanistic insights argue against possible indiscriminate use of the vaccine and activated innate immune response associated safety concerns in COVID-19, in that order.
  • |*COVID-19 Drug Treatment[MESH]
  • |Adult[MESH]
  • |Antiviral Agents/*therapeutic use[MESH]
  • |BCG Vaccine/immunology/*therapeutic use[MESH]
  • |COVID-19/epidemiology/immunology[MESH]
  • |Child[MESH]
  • |Datasets as Topic[MESH]
  • |Gene Expression Profiling[MESH]
  • |Humans[MESH]
  • |Immunity, Innate/drug effects[MESH]
  • |Infant[MESH]
  • |Respiratory Tract Infections/drug therapy/immunology[MESH]
  • |Transcriptome[MESH]


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