SARS-CoV-2 B.1.1.7 sensitivity to mRNA vaccine-elicited, convalescent and monoclonal antibodies.

COVID-19 SARS-CoV-2 antibody mutation neutralising antibodies vaccine variant

Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
15 Feb 2021
Historique:
pubmed: 24 2 2021
medline: 24 2 2021
entrez: 23 2 2021
Statut: epublish

Résumé

Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) transmission is uncontrolled in many parts of the world, compounded in some areas by higher transmission potential of the B1.1.7 variant now seen in 50 countries. It is unclear whether responses to SARS-CoV-2 vaccines based on the prototypic strain will be impacted by mutations found in B.1.1.7. Here we assessed immune responses following vaccination with mRNA-based vaccine BNT162b2. We measured neutralising antibody responses following a single immunization using pseudoviruses expressing the wild-type Spike protein or the 8 amino acid mutations found in the B.1.1.7 spike protein. The vaccine sera exhibited a broad range of neutralising titres against the wild-type pseudoviruses that were modestly reduced against B.1.1.7 variant. This reduction was also evident in sera from some convalescent patients. Decreased B.1.1.7 neutralisation was also observed with monoclonal antibodies targeting the N-terminal domain (9 out of 10), the Receptor Binding Motif (RBM) (5 out of 31), but not in neutralising mAbs binding outside the RBM. Introduction of the E484K mutation in a B.1.1.7 background to reflect newly emerging viruses in the UK led to a more substantial loss of neutralising activity by vaccine-elicited antibodies and mAbs (19 out of 31) over that conferred by the B.1.1.7 mutations alone. E484K emergence on a B.1.1.7 background represents a threat to the vaccine BNT162b.

Identifiants

pubmed: 33619509
doi: 10.1101/2021.01.19.21249840
pmc: PMC7899479
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM120553
Pays : United States
Organisme : NIAID NIH HHS
ID : DP1 AI158186
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201700059C
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R008698/1
Pays : United Kingdom

Commentaires et corrections

Type : UpdateIn

Déclaration de conflit d'intérêts

Competing interests A.D.M., J.B., D.P., C.S.F., S.B., K.C., N.S., E.C., G.S., S.J., A.L., H.W.V., M.S.P., L.P. and D.C. are employees of Vir Biotechnology and may hold shares in Vir Biotechnology. H.W.V. is a founder of PierianDx and Casma Therapeutics. Neither company provided funding for this work or is performing related work. D.V. is a consultant for Vir Biotechnology Inc. The Veesler laboratory has received a sponsored research agreement from Vir Biotechnology Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. RKG has received consulting fees from UMOVIS Lab, Gilead and ViiV.

Auteurs

Dami A Collier (DA)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.
Division of Infection and Immunity, University College London, London, UK.

Anna De Marco (A)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Isabella A T M Ferreira (IATM)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.

Bo Meng (B)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.

Rawlings Datir (R)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.
Division of Infection and Immunity, University College London, London, UK.

Alexandra C Walls (AC)

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

Steven A Kemp S (SA)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.
Division of Infection and Immunity, University College London, London, UK.

Jessica Bassi (J)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Dora Pinto (D)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Chiara Silacci Fregni (CS)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Siro Bianchi (S)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

M Alejandra Tortorici (MA)

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

John Bowen (J)

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

Katja Culap (K)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Stefano Jaconi (S)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Elisabetta Cameroni (E)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Gyorgy Snell (G)

Vir Biotechnology, San Francisco, CA 94158, USA.

Matteo S Pizzuto (MS)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Alessandra Franzetti Pellanda (AF)

Clinic of Internal Medicine and Infectious Diseases, Clinica Luganese Moncucco, 6900 Lugano, Switzerland.

Christian Garzoni (C)

Clinic of Internal Medicine and Infectious Diseases, Clinica Luganese Moncucco, 6900 Lugano, Switzerland.

Agostino Riva (A)

Division of Infectious Diseases, Luigi Sacco Hospital, University of Milan, Milan, Italy.

Anne Elmer (A)

NIHR Cambridge Clinical Research Facility, Cambridge, UK.

Nathalie Kingston (N)

NIHR Bioresource, Cambridge, UK.

Barbara Graves (B)

NIHR Bioresource, Cambridge, UK.

Laura E McCoy (LE)

Division of Infection and Immunity, University College London, London, UK.

Kenneth Gc Smith (KG)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.

John R Bradley (JR)

Department of Medicine, University of Cambridge, Cambridge, UK.
NIHR Bioresource, Cambridge, UK.

Nigel Temperton (N)

University of Kent, Canturbury, UK.

Lourdes Ceron-Gutierrez L (L)

Department of Clinical Biochemistry and Immunology, Addenbrookes Hospital, UK.

Gabriela Barcenas-Morales (G)

Department of Clinical Biochemistry and Immunology, Addenbrookes Hospital, UK.
Laboratorio de Inmunologia, S-Cuautitlán, UNAM, Mexico.

William Harvey (W)

Institute of Biodiversity, University of Glasgow, Glasgow, UK.

Herbert W Virgin (HW)

Vir Biotechnology, San Francisco, CA 94158, USA.

Antonio Lanzavecchia (A)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Luca Piccoli (L)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Rainer Doffinger (R)

Department of Clinical Biochemistry and Immunology, Addenbrookes Hospital, UK.

Mark Wills (M)

Department of Medicine, University of Cambridge, Cambridge, UK.

David Veesler (D)

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

Davide Corti (D)

Humabs Biomed SA, a subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.

Ravindra K Gupta (RK)

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.
University of KwaZulu Natal, Durban, South Africa.
Africa Health Research Institute, Durban, South Africa.
Department of Infectious Diseases, Cambridge University Hospitals NHS Trust, Cambridge UK.

Classifications MeSH