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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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          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.

          Abstract

          Antibody responses are critical for protection from developing severe COVID-19 following SARS-CoV-2 infection. Here the authors show that antibody responses against SARS-CoV-2 spike protein correlate with neutralizing capacity and protection, are not affected by heterologous boosting of influenza or common cold immunity, and can last up to 8 months.

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          Most cited references23

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          Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

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            Tracking changes in SARS-CoV-2 Spike: evidence that D614G increases infectivity of the COVID-19 virus

            Summary A SARS-CoV-2 variant carrying the Spike protein amino acid change D614G has become the most prevalent form in the global pandemic. Dynamic tracking of variant frequencies revealed a recurrent pattern of G614 increase at multiple geographic levels: national, regional and municipal. The shift occurred even in local epidemics where the original D614 form was well established prior to the introduction of the G614 variant. The consistency of this pattern was highly statistically significant, suggesting that the G614 variant may have a fitness advantage. We found that the G614 variant grows to higher titer as pseudotyped virions. In infected individuals G614 is associated with lower RT-PCR cycle thresholds, suggestive of higher upper respiratory tract viral loads, although not with increased disease severity. These findings illuminate changes important for a mechanistic understanding of the virus, and support continuing surveillance of Spike mutations to aid in the development of immunological interventions.
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              Antibody responses to SARS-CoV-2 in patients with COVID-19

              We report acute antibody responses to SARS-CoV-2 in 285 patients with COVID-19. Within 19 days after symptom onset, 100% of patients tested positive for antiviral immunoglobulin-G (IgG). Seroconversion for IgG and IgM occurred simultaneously or sequentially. Both IgG and IgM titers plateaued within 6 days after seroconversion. Serological testing may be helpful for the diagnosis of suspected patients with negative RT-PCR results and for the identification of asymptomatic infections.
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                Author and article information

                Contributors
                scarlatti.gabriella@hsr.it
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                11 May 2021
                11 May 2021
                2021
                : 12
                : 2670
                Affiliations
                [1 ]GRID grid.18887.3e, ISNI 0000000417581884, Viral Evolution and Transmission Unit, IRCCS Ospedale San Raffaele, ; Milan, Italy
                [2 ]GRID grid.18887.3e, ISNI 0000000417581884, Diabetes Research Institute, IRCCS Ospedale San Raffaele, ; Milan, Italy
                [3 ]GRID grid.416651.1, ISNI 0000 0000 9120 6856, National Center for Global Health, Istituto Superiore di Sanità, ; Rome, Italy
                [4 ]GRID grid.416651.1, ISNI 0000 0000 9120 6856, Department of Infectious Diseases, Istituto Superiore di Sanità, ; Rome, Italy
                [5 ]GRID grid.416651.1, ISNI 0000 0000 9120 6856, Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, ; Rome, Italy
                [6 ]GRID grid.18887.3e, ISNI 0000000417581884, Molecular Hematology Unit, IRCCS Ospedale San Raffaele, ; Milan, Italy
                [7 ]GRID grid.18887.3e, ISNI 0000000417581884, Hematology and Bone Marrow Transplantation Unit, IRCCS Ospedale San Raffaele, ; Milan, Italy
                [8 ]GRID grid.15496.3f, School of Medicine and Surgery, Università Vita-Salute San Raffaele, ; Milan, Italy
                [9 ]GRID grid.5326.2, ISNI 0000 0001 1940 4177, Present Address: DNA Enzymology & Molecular Virology Unit, Institute of Molecular Genetics, National Research Council, ; Pavia, Italy
                Author information
                http://orcid.org/0000-0003-1495-6778
                http://orcid.org/0000-0002-9078-8350
                http://orcid.org/0000-0003-4967-1895
                http://orcid.org/0000-0003-2316-2689
                Article
                22958
                10.1038/s41467-021-22958-8
                8113594
                33976165
                86272b47-142d-46ad-acca-3e179d1fbd6a
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 January 2021
                : 11 April 2021
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100003196, Ministero della Salute (Ministry of Health, Italy);
                Award ID: COVID-2020-12371617
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100010661, EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020);
                Award ID: 681137
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100004415, North Atlantic Treaty Organization (NATO);
                Award ID: G5817
                Award Recipient :
                Funded by: Fondation Dormeur, Vaduz.
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                humoral immunity,antimicrobial responses,viral infection,infection
                Uncategorized
                humoral immunity, antimicrobial responses, viral infection, infection

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