No retraction, correction or concern found when last checked on Oct 31, 2026.
SARS-CoV-2 escape from a highly neutralizing COVID-19 convalescent plasma
Emanuele Andreano, Giulia Piccini, Danilo Licastro and 15 more
Proceedings of the National Academy of Sciences · 2021 · CC BY
Abstract
Significance This work shows that, under strong immune pressure, SARS-CoV-2 can use mutations in both the N-terminal domain and the receptor-binding domain to escape potent polyclonal neutralizing responses. Indeed, after a long period under immune selective pressure, SARS-CoV-2 evolved to evade the immunity of a potent polyclonal serum from a COVID-19 convalescent donor. Only three mutations were sufficient to generate this escape variant. The new virus was resistant to 70% of the neutralizing antibodies tested and had a decreased susceptibility to all convalescent sera. Our data predict that, as the immunity in the population increases, following infection and vaccination, new variants will emerge, and therefore vaccines and monoclonal antibodies need to be developed to address them.
Cited by papers we hold 22
- The Substitutions L50F, E166A, and L167F in SARS-CoV-2 3CLpro Are Selected by a Protease Inhibitor In Vitro and Confer Resistance To Nirmatrelvir · 2023No notice
- Emergence of a novel SARS-CoV-2 Pango lineage B.1.1.526 in West Bengal, India · 2022Not checked
- The SARS-CoV-2 mutations versus vaccine effectiveness: New opportunities to new challenges · 2022No notice
- Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera · 2021No notice
- Vaccines against Covid-19: Comparison, Limitations, the Decrease of Pandemic and the Perspective of Viral Respiratory · 2021Not checked
- Prolonged evolution of the human B cell response to SARS-CoV-2 infection · 2021No notice
- SARS CoV-2 Delta variant exhibits enhanced infectivity and a minor decrease in neutralization sensitivity to convalescent or post-vaccination sera · 2021Not checked
- A Combination of Receptor-Binding Domain and N-Terminal Domain Neutralizing Antibodies Limits the Generation of SARS-CoV-2 Spike Neutralization-Escape Mutants · 2021Not checked
- Experimental Evidence for Enhanced Receptor Binding by Rapidly Spreading SARS-CoV-2 Variants · 2021No notice
- Within-host evolution of SARS-CoV-2 in an immunosuppressed COVID-19 patient as a source of immune escape variants · 2021No notice
- A novel diagnostic test to screen SARS-CoV-2 variants containing E484K and N501Y mutations · 2021Not checked
- Complete map of SARS-CoV-2 RBD mutations that escape the monoclonal antibody LY-CoV555 and its cocktail with LY-CoV016 · 2021No notice
- SARS-CoV-2 immune evasion by the B.1.427/B.1.429 variant of concern · 2021No notice
- Sensitivity of SARS-CoV-2 B.1.1.7 to mRNA vaccine-elicited antibodies · 2021Corrected
- Mapping mutations to the SARS-CoV-2 RBD that escape binding by different classes of antibodies · 2021No notice
- Potent and protective IGHV3-53/3-66 public antibodies and their shared escape mutant on the spike of SARS-CoV-2 · 2021No notice
- Immune Evasion of SARS-CoV-2 Emerging Variants: What Have We Learnt So Far? · 2021No notice
- SARS-CoV-2 one year on: evidence for ongoing viral adaptation · 2021No notice
- Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice · 2021No notice
- Scientific rationale for developing potent RBD-based vaccines targeting COVID-19 · 2021No notice
and 2 more
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.