Matches in SemOpenAlex for { <https://semopenalex.org/work/W3201232207> ?p ?o ?g. }
- W3201232207 endingPage "97" @default.
- W3201232207 startingPage "49" @default.
- W3201232207 abstract "Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections trigger viral RNA sensors such as TLR7 and RIG-I, thereby leading to production of type I interferon (IFN) and other inflammatory mediators. Expression of viral proteins in the context of this inflammation leads to stereotypical antigen-specific antibody and T cell responses that clear the virus. Immunity is then maintained through long-lived antibody-secreting plasma cells and by memory B and T cells that can initiate anamnestic responses. Each of these steps is consistent with prior knowledge of acute RNA virus infections. Yet there are certain concepts, while not entirely new, that have been resurrected by the biology of severe SARS-CoV-2 infections and deserve further attention. These include production of anti-IFN autoantibodies, early inflammatory processes that slow adaptive humoral immunity, immunodominance of antibody responses, and original antigenic sin. Moreover, multiple different vaccine platforms allow for comparisons of pathways that promote robust and durable adaptive immunity." @default.
- W3201232207 created "2021-09-27" @default.
- W3201232207 creator A5011630697 @default.
- W3201232207 creator A5067384764 @default.
- W3201232207 date "2021-01-01" @default.
- W3201232207 modified "2023-09-30" @default.
- W3201232207 title "Immunology of SARS-CoV-2 infections and vaccines" @default.
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