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10.1016/j.celrep.2021.108890

http://scihub22266oqcxt.onion/10.1016/j.celrep.2021.108890
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33713594!7936541!33713594
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suck abstract from ncbi


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pmid33713594      Cell+Rep 2021 ; 34 (12): 108890
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  • The effect of spike mutations on SARS-CoV-2 neutralization #MMPMID33713594
  • Rees-Spear C; Muir L; Griffith SA; Heaney J; Aldon Y; Snitselaar JL; Thomas P; Graham C; Seow J; Lee N; Rosa A; Roustan C; Houlihan CF; Sanders RW; Gupta RK; Cherepanov P; Stauss HJ; Nastouli E; Doores KJ; van Gils MJ; McCoy LE
  • Cell Rep 2021[Mar]; 34 (12): 108890 PMID33713594show ga
  • Multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines show protective efficacy, which is most likely mediated by neutralizing antibodies recognizing the viral entry protein, spike. Because new SARS-CoV-2 variants are emerging rapidly, as exemplified by the B.1.1.7, B.1.351, and P.1 lineages, it is critical to understand whether antibody responses induced by infection with the original SARS-CoV-2 virus or current vaccines remain effective. In this study, we evaluate neutralization of a series of mutated spike pseudotypes based on divergence from SARS-CoV and then compare neutralization of the B.1.1.7 spike pseudotype and individual mutations. Spike-specific monoclonal antibody neutralization is reduced dramatically; in contrast, polyclonal antibodies from individuals infected in early 2020 remain active against most mutated spike pseudotypes, but potency is reduced in a minority of samples. This work highlights that changes in SARS-CoV-2 spike can alter neutralization sensitivity and underlines the need for effective real-time monitoring of emerging mutations and their effect on vaccine efficacy.
  • |Antibodies, Monoclonal/genetics/immunology[MESH]
  • |Antibodies, Neutralizing/*immunology[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |Antibody Formation[MESH]
  • |COVID-19 Vaccines/immunology[MESH]
  • |COVID-19/immunology/metabolism/*virology[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Neutralization Tests/methods[MESH]
  • |Point Mutation[MESH]
  • |Receptors, Virus/genetics/metabolism[MESH]
  • |SARS-CoV-2/*genetics/*immunology[MESH]


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