Sotrovimab therapy elicits antiviral activities against Omicron BQ.1.1 and XBB.1.5 in sera of immunocompromised patients

Antibodies effective against the recent Omicron sublineages are missing. By taking advantage of a multi-centric prospective cohort of immunocompromised individuals treated for mild-to-moderate COVID-19, Bruel et al. show that administration of 500 mg of sotrovimab induces serum neutralization and an...

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Published inMed (New York, N.Y. : Online) Vol. 4; no. 10; pp. 664 - 667
Main Authors Bruel, Timothée, Vrignaud, Lou-Léna, Porrot, Françoise, Planas, Delphine, Puech, Julien, Munier, Sandie, Soulié, Cathia, Zafilaza, Karen, Molino, Diana, Péré, Hélène, Yordanov, Youri, Veyer, David, Carrat, Fabrice, Schwartz, Olivier, Marcelin, Anne-Geneviève, Giraud, Valentin, Cazenave-Roblot, Fance, Martellosio Anne-Marie Ronchetti, Jean-Philippe, Gabas, Thomas, Housset, Pierre, Pardon, Agathe, Faucon, Anne-Laure, Alric, Laurent, Mourguet, Morgane, Bonnet, Delphine, Delobel, Pierre, Beck, Colleen, Boumaza, Xavier, Delage, Claire, Pires, Elisabete Gomes, Cheminant, Morgane, Anthony Chauvin, Nathalie Chavarot, Cresta, Mélanie, Pélagie Thibaut, Romain Gueneau, Siguier, Martin, Faycal, Antoine, Brin, Cécile, Djebara, Siham, Sayon, Sophie, Leducq, Vincent, Malet, Isabelle, Teyssou, Elisa, Karine Lacombe, Adélie Gothland, Chiarabini, Thibault, Valin, Nadia, Boize, Julien, Thiébaud, Pierre-Clément, Moreau, Marie, Nathalie De Castro, Charlotte Billard, Denis, Blandine, Molina, Jean-Michel, André Cabié, Lucia Etheve, Cabras, Ornella, François Vincent Dubee, Sandrine Pierre, Pistone, Thierry, Desclaux, Arnaud, Festou, Benjamin, Nathan Peiffer- Smadja, Delphine Chainier, Thy, Michael, Godard, Cindy, Bouzid, Donia, Ing, Vittiaroat, Pereira, Laurent, Pavlowsky, Thomas, Boutoille, David, Deschanvres, Colin, Cailleaux, Marine, Benezit, François, Maillard, Anne, François Coustilleres, Pierre Tattevin, Vidal, Magali, Sauvat, Léo, Baronnet, Guillaume, Florence Ader, Agnès Didier, Perpoint, Thomas, Conrad, Anne, Chabert, Paul, Loubet, Paul, Mazet, Julien, Remillon, Aline, Albert Trinh-Duc, Pauline Bouquet, Philippe Petua, Patrick Rispal, Aurore Perrot, Julien Carillo, Cougoul, Pierre, Dion, Jérémie, Mathieu Blot, Odile Rauzy, Sixt, Thibault, Moretto, Florian, Charles, Carole, Sophie Circosta, Lionel Piroth, Leger, Lydia, Arulananthan, Arulvani, Lascoux, Carine, Yazdan Yazdanpanah, Leia Becam, Petrov-Sanchez, Ventzislava, Le Mestre, Soizic, Chau, Frédéric, Soltana, Brahim, Caille, Yvanie
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 13.10.2023
Cell Press
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Summary:Antibodies effective against the recent Omicron sublineages are missing. By taking advantage of a multi-centric prospective cohort of immunocompromised individuals treated for mild-to-moderate COVID-19, Bruel et al. show that administration of 500 mg of sotrovimab induces serum neutralization and antibody-dependent cellular cytotoxicity of BQ.1.1 and XBB.1.5. Therefore, sotrovimab may remain a therapeutic option against these variants. Antibodies effective against the recent Omicron sublineages are missing. By taking advantage of a multi-centric prospective cohort of immunocompromised individuals treated for mild-to-moderate COVID-19, Bruel et al. show that administration of 500 mg of sotrovimab induces serum neutralization and antibody-dependent cellular cytotoxicity of BQ.1.1 and XBB.1.5. Therefore, sotrovimab may remain a therapeutic option against these variants.
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content type line 23
PMCID: PMC11232389
Lead Contact
T.B., O.S., A.G.M. and G.M.B. designed the overall experiments, wrote the article, and had unrestricted access to all data. T.B., L.L.V, F.P, I.S, D.P, F.G., O.S. performed the experiments. C.S., K.Z., C.L.N, M.L.M., C.D., D.M., Y.Y., F. C., A.G.M., G.M.B., & C.S.G. managed the cohort. J.P., M.P., S.M., H.P., E.S.L., & D.V. provided key reagents and/or viral strains. T.B., C.L.N., M.L.N., O.S., A.G.M. & G.M.B. performed statistical analyses. All authors read and approved the final article and take responsibility for its content.
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ISSN:2666-6340
2666-6359
2666-6340
DOI:10.1016/j.medj.2023.07.007