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10.3390/vaccines8040700

http://scihub22266oqcxt.onion/10.3390/vaccines8040700
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33233531!7711778!33233531
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suck abstract from ncbi


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pmid33233531      Vaccines+(Basel) 2020 ; 8 (4): ä
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  • Immunogenetic Association Underlying Severe COVID-19 #MMPMID33233531
  • McCoy K; Peterson A; Tian Y; Sang Y
  • Vaccines (Basel) 2020[Nov]; 8 (4): ä PMID33233531show ga
  • SARS-CoV2 has caused the current pandemic of new coronavirus disease 2019 (COVID-19) worldwide. Clinical outcomes of COVID-19 illness range broadly from asymptotic and mild to a life-threatening situation. This casts uncertainties for defining host determinants underlying the disease severity. Recent genetic analyses based on extensive clinical sample cohorts using genome-wide association studies (GWAS) and high throughput sequencing curation revealed genetic errors and gene loci associated with about 20% of life-threatening COVID-19 cases. Significantly, most of these critical genetic loci are enriched in two immune signaling pathways, i.e., interferon-mediated antiviral signaling and chemokine-mediated/inflammatory signaling. In line with these genetic profiling studies, the broad spectrum of COVID-19 illness could be explained by immuno-pathological regulation of these critical immunogenetic pathways through various epigenetic mechanisms, which further interconnect to other vital components such as those in the renin-angiotensin-aldosterone system (RAAS) because of its direct interaction with the virus causing COVID-19. Together, key genes unraveled by genetic profiling may provide targets for precisely early risk diagnosis and prophylactic design to relieve severe COVID-19. The confounding epigenetic mechanisms may be key to understanding the clinical broadness of COVID-19 illness.
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