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

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  • Stefania Dispinseri

    (Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele)

  • Massimiliano Secchi

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele
    DNA Enzymology & Molecular Virology Unit, Institute of Molecular Genetics, National Research Council)

  • Maria Franca Pirillo

    (National Center for Global Health, Istituto Superiore di Sanità)

  • Monica Tolazzi

    (Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele)

  • Martina Borghi

    (Department of Infectious Diseases, Istituto Superiore di Sanità)

  • Cristina Brigatti

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele)

  • Maria Laura Angelis

    (Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità)

  • Marco Baratella

    (Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele)

  • Elena Bazzigaluppi

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele)

  • Giulietta Venturi

    (Department of Infectious Diseases, Istituto Superiore di Sanità)

  • Francesca Sironi

    (Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele)

  • Andrea Canitano

    (National Center for Global Health, Istituto Superiore di Sanità)

  • Ilaria Marzinotto

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele)

  • Cristina Tresoldi

    (Molecular Hematology Unit, IRCCS Ospedale San Raffaele)

  • Fabio Ciceri

    (Hematology and Bone Marrow Transplantation Unit, IRCCS Ospedale San Raffaele
    School of Medicine and Surgery, Università Vita-Salute San Raffaele)

  • Lorenzo Piemonti

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele
    School of Medicine and Surgery, Università Vita-Salute San Raffaele)

  • Donatella Negri

    (Department of Infectious Diseases, Istituto Superiore di Sanità)

  • Andrea Cara

    (National Center for Global Health, Istituto Superiore di Sanità)

  • Vito Lampasona

    (Diabetes Research Institute, IRCCS Ospedale San Raffaele)

  • Gabriella Scarlatti

    (Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele)

Abstract

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.

Suggested Citation

  • Stefania Dispinseri & Massimiliano Secchi & Maria Franca Pirillo & Monica Tolazzi & Martina Borghi & Cristina Brigatti & Maria Laura Angelis & Marco Baratella & Elena Bazzigaluppi & Giulietta Venturi , 2021. "Neutralizing antibody responses to SARS-CoV-2 in symptomatic COVID-19 is persistent and critical for survival," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-22958-8
    DOI: 10.1038/s41467-021-22958-8
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    Cited by:

    1. Dennis Lapuente & Jana Fuchs & Jonas Willar & Ana Vieira Antão & Valentina Eberlein & Nadja Uhlig & Leila Issmail & Anna Schmidt & Friederike Oltmanns & Antonia Sophia Peter & Sandra Mueller-Schmucker, 2021. "Protective mucosal immunity against SARS-CoV-2 after heterologous systemic prime-mucosal boost immunization," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
    2. Kenneth Danh & Donna Grace Karp & Malvika Singhal & Akshaya Tankasala & David Gebhart & Felipe Jesus Cortez & Devangkumar Tandel & Peter V. Robinson & David Seftel & Mars Stone & Graham Simmons & Anil, 2022. "Detection of neutralizing antibodies against multiple SARS-CoV-2 strains in dried blood spots using cell-free PCR," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    3. Simone Lanini & Stefano Milleri & Emanuele Andreano & Sarah Nosari & Ida Paciello & Giulia Piccini & Alessandra Gentili & Adhuna Phogat & Inesa Hyseni & Margherita Leonardi & Alessandro Torelli & Eman, 2022. "Safety and serum distribution of anti-SARS-CoV-2 monoclonal antibody MAD0004J08 after intramuscular injection," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    4. Grace Kenny & Sophie O’Reilly & Neil Wrigley Kelly & Riya Negi & Colette Gaillard & Dana Alalwan & Gurvin Saini & Tamara Alrawahneh & Nathan Francois & Matthew Angeliadis & Alejandro Abner Garcia Leon, 2023. "Distinct receptor binding domain IgG thresholds predict protective host immunity across SARS-CoV-2 variants and time," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    5. Sun Jin Kim & Zhong Yao & Morgan C. Marsh & Debra M. Eckert & Michael S. Kay & Anna Lyakisheva & Maria Pasic & Aiyush Bansal & Chaim Birnboim & Prabhat Jha & Yannick Galipeau & Marc-André Langlois & J, 2022. "Homogeneous surrogate virus neutralization assay to rapidly assess neutralization activity of anti-SARS-CoV-2 antibodies," Nature Communications, Nature, vol. 13(1), pages 1-9, December.

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