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10.3389/fmed.2021.679030

http://scihub22266oqcxt.onion/10.3389/fmed.2021.679030
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suck abstract from ncbi


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pmid34368185      Front+Med+(Lausanne) 2021 ; 8 (ä): 679030
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  • Potential Implications of a Type 1 Interferon Gene Signature on COVID-19 Severity and Chronic Inflammation in Sickle Cell Disease #MMPMID34368185
  • Madany E; Okwan-Duodu D; Balbuena-Merle R; Hendrickson JE; Gibb DR
  • Front Med (Lausanne) 2021[]; 8 (ä): 679030 PMID34368185show ga
  • At the onset of the corona virus disease 19 (COVID-19) pandemic, there were concerns that patients with sickle cell disease (SCD) might be especially vulnerable to severe sequelae of SARS-CoV-2 infection. While two reports support this conclusion, multiple studies have reported unexpectedly favorable outcomes in patients with SCD. However, mechanisms explaining these disparate conclusions are lacking. Here, we review recent studies indicating that the majority of patients with SCD express elevated levels of anti-viral type 1 interferons (IFNalpha/beta) and interferon stimulated genes, independent of COVID-19, during their baseline state of health. We also present our data from the pre-COVID-19 era, illustrating elevated expression of a well-characterized interferon stimulated gene in a cohort of patients with SCD, compared to race-matched controls. These type 1 interferons and interferon stimulated genes have the potential to contribute to the variable progression of COVID-19 and other viral infections in patients with SCD. While the majority of evidence supports a protective role, the role of IFNalpha/beta in COVID-19 severity in the general population remains an area of current investigation. We conclude that type 1 interferon responses in patients with SCD may contribute to the variable COVID-19 responses reported in prior studies. Additional studies investigating the mechanisms underlying IFNalpha/beta production and other clinical consequences of IFNalpha/beta-mediated inflammation in SCD disease are warranted.
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