Neutralizing antibody responses to SARS-CoV-2 in symptomatic COVID-19 is persistent and critical for survival.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
11 05 2021
Historique:
received: 27 01 2021
accepted: 11 04 2021
entrez: 12 5 2021
pubmed: 13 5 2021
medline: 22 5 2021
Statut: epublish

Résumé

Understanding how antibody responses to SARS-CoV-2 evolve during infection may provide important insight into therapeutic approaches and vaccination for COVID-19. Here we profile the antibody responses of 162 COVID-19 symptomatic patients in the COVID-BioB cohort followed longitudinally for up to eight months from symptom onset to find SARS-CoV-2 neutralization, as well as antibodies either recognizing SARS-CoV-2 spike antigens and nucleoprotein, or specific for S2 antigen of seasonal beta-coronaviruses and hemagglutinin of the H1N1 flu virus. The presence of neutralizing antibodies within the first weeks from symptoms onset correlates with time to a negative swab result (p = 0.002), while the lack of neutralizing capacity correlates with an increased risk of a fatal outcome (p = 0.008). Neutralizing antibody titers progressively drop after 5-8 weeks but are still detectable up to 8 months in the majority of recovered patients regardless of age or co-morbidities, with IgG to spike antigens providing the best correlate of neutralization. Antibody responses to seasonal coronaviruses are temporarily boosted, and parallel those to SARS-CoV-2 without dampening the specific response or worsening disease progression. Our results thus suggest compromised immune responses to the SARS-CoV-2 spike to be a major trait of COVID-19 patients with critical conditions, and thereby inform on the planning of COVID-19 patient care and therapy prioritization.

Identifiants

pubmed: 33976165
doi: 10.1038/s41467-021-22958-8
pii: 10.1038/s41467-021-22958-8
pmc: PMC8113594
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2670

Subventions

Organisme : Ministero della Salute (Ministry of Health, Italy)
ID : COVID-2020-12371617
Organisme : EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020)
ID : 681137
Organisme : North Atlantic Treaty Organization (NATO)
ID : G5817

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Auteurs

Stefania Dispinseri (S)

Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Massimiliano Secchi (M)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.
DNA Enzymology & Molecular Virology Unit, Institute of Molecular Genetics, National Research Council, Pavia, Italy.

Maria Franca Pirillo (MF)

National Center for Global Health, Istituto Superiore di Sanità, Rome, Italy.

Monica Tolazzi (M)

Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Martina Borghi (M)

Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.

Cristina Brigatti (C)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Maria Laura De Angelis (ML)

Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.

Marco Baratella (M)

Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Elena Bazzigaluppi (E)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Giulietta Venturi (G)

Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.

Francesca Sironi (F)

Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Andrea Canitano (A)

National Center for Global Health, Istituto Superiore di Sanità, Rome, Italy.

Ilaria Marzinotto (I)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Cristina Tresoldi (C)

Molecular Hematology Unit, IRCCS Ospedale San Raffaele, Milan, Italy.

Fabio Ciceri (F)

Hematology and Bone Marrow Transplantation Unit, IRCCS Ospedale San Raffaele, Milan, Italy.
School of Medicine and Surgery, Università Vita-Salute San Raffaele, Milan, Italy.

Lorenzo Piemonti (L)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.
School of Medicine and Surgery, Università Vita-Salute San Raffaele, Milan, Italy.

Donatella Negri (D)

Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.

Andrea Cara (A)

National Center for Global Health, Istituto Superiore di Sanità, Rome, Italy.

Vito Lampasona (V)

Diabetes Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Gabriella Scarlatti (G)

Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, Milan, Italy. scarlatti.gabriella@hsr.it.

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Classifications MeSH