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10.1016/j.chom.2021.03.009

http://scihub22266oqcxt.onion/10.1016/j.chom.2021.03.009
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suck abstract from ncbi


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pmid33798491      Cell+Host+Microbe 2021 ; 29 (4): 516-521.e3
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  • Infection- and vaccine-induced antibody binding and neutralization of the B 1 351 SARS-CoV-2 variant #MMPMID33798491
  • Edara VV; Norwood C; Floyd K; Lai L; Davis-Gardner ME; Hudson WH; Mantus G; Nyhoff LE; Adelman MW; Fineman R; Patel S; Byram R; Gomes DN; Michael G; Abdullahi H; Beydoun N; Panganiban B; McNair N; Hellmeister K; Pitts J; Winters J; Kleinhenz J; Usher J; O'Keefe JB; Piantadosi A; Waggoner JJ; Babiker A; Stephens DS; Anderson EJ; Edupuganti S; Rouphael N; Ahmed R; Wrammert J; Suthar MS
  • Cell Host Microbe 2021[Apr]; 29 (4): 516-521.e3 PMID33798491show ga
  • The emergence of SARS-CoV-2 variants with mutations in the spike protein is raising concerns about the efficacy of infection- or vaccine-induced antibodies. We compared antibody binding and live virus neutralization of sera from naturally infected and Moderna-vaccinated individuals against two SARS-CoV-2 variants: B.1 containing the spike mutation D614G and the emerging B.1.351 variant containing additional spike mutations and deletions. Sera from acutely infected and convalescent COVID-19 patients exhibited a 3-fold reduction in binding antibody titers to the B.1.351 variant receptor-binding domain of the spike protein and a 3.5-fold reduction in neutralizing antibody titers against SARS-CoV-2 B.1.351 variant compared to the B.1 variant. Similar results were seen with sera from Moderna-vaccinated individuals. Despite reduced antibody titers against the B.1.351 variant, sera from infected and vaccinated individuals containing polyclonal antibodies to the spike protein could still neutralize SARS-CoV-2 B.1.351, suggesting that protective humoral immunity may be retained against this variant.
  • |Antibodies, Neutralizing/*immunology[MESH]
  • |Antibodies, Viral/*immunology[MESH]
  • |Binding Sites[MESH]
  • |COVID-19 Vaccines/*immunology[MESH]
  • |COVID-19/*immunology/prevention & control[MESH]
  • |Humans[MESH]
  • |Neutralization Tests[MESH]
  • |Receptors, Virus/chemistry[MESH]


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