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10.1002/rmv.2231

http://scihub22266oqcxt.onion/10.1002/rmv.2231
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33724631!8250244!33724631
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suck abstract from ncbi


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pmid33724631      Rev+Med+Virol 2021 ; 31 (6): e2231
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  • Neutralising antibody escape of SARS-CoV-2 spike protein: Risk assessment for antibody-based Covid-19 therapeutics and vaccines #MMPMID33724631
  • Focosi D; Maggi F
  • Rev Med Virol 2021[Nov]; 31 (6): e2231 PMID33724631show ga
  • The Spike protein is the target of both antibody-based therapeutics (convalescent plasma, polyclonal serum, monoclonal antibodies) and vaccines. Mutations in Spike could affect efficacy of those treatments. Hence, monitoring of mutations is necessary to forecast and readapt the inventory of therapeutics. Different phylogenetic nomenclatures have been used for the currently circulating SARS-CoV-2 clades. The Spike protein has different hotspots of mutation and deletion, the most dangerous for immune escape being the ones within the receptor binding domain (RBD), such as K417N/T, N439K, L452R, Y453F, S477N, E484K, and N501Y. Convergent evolution has led to different combinations of mutations among different clades. In this review we focus on the main variants of concern, that is, the so-called UK (B.1.1.7), South African (B.1.351) and Brazilian (P.1) strains.
  • |Antibodies, Monoclonal/chemistry/metabolism/*therapeutic use[MESH]
  • |Antibodies, Neutralizing/chemistry/metabolism/*therapeutic use[MESH]
  • |Antibodies, Viral/chemistry/metabolism/therapeutic use[MESH]
  • |Brazil/epidemiology[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19 Vaccines/administration & dosage[MESH]
  • |COVID-19/epidemiology/immunology/*therapy/virology[MESH]
  • |Gene Expression[MESH]
  • |Humans[MESH]
  • |Immune Evasion[MESH]
  • |Immunization, Passive/methods[MESH]
  • |Mutation[MESH]
  • |Phylogeny[MESH]
  • |Protein Binding[MESH]
  • |Risk Assessment[MESH]
  • |SARS-CoV-2/classification/drug effects/*genetics/immunology[MESH]
  • |South Africa/epidemiology[MESH]
  • |Spike Glycoprotein, Coronavirus/*genetics/immunology[MESH]


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