Cargando…
Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies
Convergent evolution of SARS-CoV-2 Omicron BA.2, BA.4 and BA.5 lineages has led to the emergence of several new subvariants, including BA.2.75.2, BA.4.6. and BQ.1.1. The subvariants BA.2.75.2 and BQ.1.1 are expected to become predominant in many countries in November 2022. They carry an additional a...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681044/ https://www.ncbi.nlm.nih.gov/pubmed/36415455 http://dx.doi.org/10.1101/2022.11.17.516888 |
_version_ | 1784834531244638208 |
---|---|
author | Planas, Delphine Bruel, Timothée Staropoli, Isabelle Guivel-Benhassine, Florence Porrot, Françoise Maes, Piet Grzelak, Ludivine Prot, Matthieu Mougari, Said Planchais, Cyril Puech, Julien Saliba, Madelina Sahraoui, Riwan Fémy, Florent Morel, Nathalie Dufloo, Jérémy Sanjuán, Rafael Mouquet, Hugo André, Emmanuel Hocqueloux, Laurent Simon-Loriere, Etienne Veyer, David Prazuck, Thierry Péré, Hélène Schwartz, Olivier |
author_facet | Planas, Delphine Bruel, Timothée Staropoli, Isabelle Guivel-Benhassine, Florence Porrot, Françoise Maes, Piet Grzelak, Ludivine Prot, Matthieu Mougari, Said Planchais, Cyril Puech, Julien Saliba, Madelina Sahraoui, Riwan Fémy, Florent Morel, Nathalie Dufloo, Jérémy Sanjuán, Rafael Mouquet, Hugo André, Emmanuel Hocqueloux, Laurent Simon-Loriere, Etienne Veyer, David Prazuck, Thierry Péré, Hélène Schwartz, Olivier |
author_sort | Planas, Delphine |
collection | PubMed |
description | Convergent evolution of SARS-CoV-2 Omicron BA.2, BA.4 and BA.5 lineages has led to the emergence of several new subvariants, including BA.2.75.2, BA.4.6. and BQ.1.1. The subvariants BA.2.75.2 and BQ.1.1 are expected to become predominant in many countries in November 2022. They carry an additional and often redundant set of mutations in the spike, likely responsible for increased transmissibility and immune evasion. Here, we established a viral amplification procedure to easily isolate Omicron strains. We examined their sensitivity to 6 therapeutic monoclonal antibodies (mAbs) and to 72 sera from Pfizer BNT162b2-vaccinated individuals, with or without BA.1/BA.2 or BA.5 breakthrough infection. Ronapreve (Casirivimab and Imdevimab) and Evusheld (Cilgavimab and Tixagevimab) lost any antiviral efficacy against BA.2.75.2 and BQ.1.1, whereas Xevudy (Sotrovimab) remained weakly active. BQ.1.1 was also resistant to Bebtelovimab. Neutralizing titers in triply vaccinated individuals were low to undetectable against BQ.1.1 and BA.2.75.2, 4 months after boosting. A BA.1/BA.2 breakthrough infection increased these titers, which remained about 18-fold lower against BA.2.75.2 and BQ.1.1, than against BA.1. Reciprocally, a BA.5 breakthrough infection increased more efficiently neutralization against BA.5 and BQ.1.1 than against BA.2.75.2. Thus, the evolution trajectory of novel Omicron subvariants facilitated their spread in immunized populations and raises concerns about the efficacy of most currently available mAbs. |
format | Online Article Text |
id | pubmed-9681044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-96810442022-11-23 Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies Planas, Delphine Bruel, Timothée Staropoli, Isabelle Guivel-Benhassine, Florence Porrot, Françoise Maes, Piet Grzelak, Ludivine Prot, Matthieu Mougari, Said Planchais, Cyril Puech, Julien Saliba, Madelina Sahraoui, Riwan Fémy, Florent Morel, Nathalie Dufloo, Jérémy Sanjuán, Rafael Mouquet, Hugo André, Emmanuel Hocqueloux, Laurent Simon-Loriere, Etienne Veyer, David Prazuck, Thierry Péré, Hélène Schwartz, Olivier bioRxiv Article Convergent evolution of SARS-CoV-2 Omicron BA.2, BA.4 and BA.5 lineages has led to the emergence of several new subvariants, including BA.2.75.2, BA.4.6. and BQ.1.1. The subvariants BA.2.75.2 and BQ.1.1 are expected to become predominant in many countries in November 2022. They carry an additional and often redundant set of mutations in the spike, likely responsible for increased transmissibility and immune evasion. Here, we established a viral amplification procedure to easily isolate Omicron strains. We examined their sensitivity to 6 therapeutic monoclonal antibodies (mAbs) and to 72 sera from Pfizer BNT162b2-vaccinated individuals, with or without BA.1/BA.2 or BA.5 breakthrough infection. Ronapreve (Casirivimab and Imdevimab) and Evusheld (Cilgavimab and Tixagevimab) lost any antiviral efficacy against BA.2.75.2 and BQ.1.1, whereas Xevudy (Sotrovimab) remained weakly active. BQ.1.1 was also resistant to Bebtelovimab. Neutralizing titers in triply vaccinated individuals were low to undetectable against BQ.1.1 and BA.2.75.2, 4 months after boosting. A BA.1/BA.2 breakthrough infection increased these titers, which remained about 18-fold lower against BA.2.75.2 and BQ.1.1, than against BA.1. Reciprocally, a BA.5 breakthrough infection increased more efficiently neutralization against BA.5 and BQ.1.1 than against BA.2.75.2. Thus, the evolution trajectory of novel Omicron subvariants facilitated their spread in immunized populations and raises concerns about the efficacy of most currently available mAbs. Cold Spring Harbor Laboratory 2022-11-21 /pmc/articles/PMC9681044/ /pubmed/36415455 http://dx.doi.org/10.1101/2022.11.17.516888 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Planas, Delphine Bruel, Timothée Staropoli, Isabelle Guivel-Benhassine, Florence Porrot, Françoise Maes, Piet Grzelak, Ludivine Prot, Matthieu Mougari, Said Planchais, Cyril Puech, Julien Saliba, Madelina Sahraoui, Riwan Fémy, Florent Morel, Nathalie Dufloo, Jérémy Sanjuán, Rafael Mouquet, Hugo André, Emmanuel Hocqueloux, Laurent Simon-Loriere, Etienne Veyer, David Prazuck, Thierry Péré, Hélène Schwartz, Olivier Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title | Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title_full | Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title_fullStr | Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title_full_unstemmed | Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title_short | Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies |
title_sort | resistance of omicron subvariants ba.2.75.2, ba.4.6 and bq.1.1 to neutralizing antibodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9681044/ https://www.ncbi.nlm.nih.gov/pubmed/36415455 http://dx.doi.org/10.1101/2022.11.17.516888 |
work_keys_str_mv | AT planasdelphine resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT brueltimothee resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT staropoliisabelle resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT guivelbenhassineflorence resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT porrotfrancoise resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT maespiet resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT grzelakludivine resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT protmatthieu resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT mougarisaid resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT planchaiscyril resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT puechjulien resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT salibamadelina resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT sahraouiriwan resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT femyflorent resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT morelnathalie resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT dufloojeremy resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT sanjuanrafael resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT mouquethugo resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT andreemmanuel resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT hocquelouxlaurent resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT simonloriereetienne resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT veyerdavid resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT prazuckthierry resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT perehelene resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies AT schwartzolivier resistanceofomicronsubvariantsba2752ba46andbq11toneutralizingantibodies |