Persistence of neutralizing antibodies a year after SARS‐CoV‐2 infection in humans
Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV...
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Published in | European journal of immunology Vol. 51; no. 12; pp. 3202 - 3213 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
01.12.2021
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0014-2980 1521-4141 1521-4141 |
DOI | 10.1002/eji.202149535 |
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Abstract | Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV‐2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS‐CoV‐2 spike IgG (S‐IgG) and nucleoprotein IgG (N‐IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants (n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S‐IgG in 97% of subjects for at least 13 months after infection. Only 36% had N‐IgG by 13 months. The mean S‐IgG concentrations declined from 8 to 13 months by less than one third; N‐IgG concentrations declined by two‐thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs.
A year after WT SARS‐CoV‐2 infection high seropositivity rate was observed: 89% of subjects had persisting neutralizing antibodies and up to 97% had anti‐spike IgG antibodies. Compared to the WT virus, neutralizing antibody titers were reduced for variants of concern Alpha, Beta, and Delta. |
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AbstractList | Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV‐2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS‐CoV‐2 spike IgG (S‐IgG) and nucleoprotein IgG (N‐IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants (n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S‐IgG in 97% of subjects for at least 13 months after infection. Only 36% had N‐IgG by 13 months. The mean S‐IgG concentrations declined from 8 to 13 months by less than one third; N‐IgG concentrations declined by two‐thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs.
A year after WT SARS‐CoV‐2 infection high seropositivity rate was observed: 89% of subjects had persisting neutralizing antibodies and up to 97% had anti‐spike IgG antibodies. Compared to the WT virus, neutralizing antibody titers were reduced for variants of concern Alpha, Beta, and Delta. Most subjects develop antibodies to SARS-CoV-2 following infection. In order to estimate the duration of immunity induced by SARS-CoV-2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS-CoV-2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS-CoV-2 spike IgG (S-IgG) and nucleoprotein IgG (N-IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants (n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S-IgG in 97% of subjects for at least 13 months after infection. Only 36% had N-IgG by 13 months. The mean S-IgG concentrations declined from 8 to 13 months by less than one third; N-IgG concentrations declined by two-thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs.Most subjects develop antibodies to SARS-CoV-2 following infection. In order to estimate the duration of immunity induced by SARS-CoV-2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS-CoV-2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS-CoV-2 spike IgG (S-IgG) and nucleoprotein IgG (N-IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants (n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S-IgG in 97% of subjects for at least 13 months after infection. Only 36% had N-IgG by 13 months. The mean S-IgG concentrations declined from 8 to 13 months by less than one third; N-IgG concentrations declined by two-thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs. Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV‐2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS‐CoV‐2 spike IgG (S‐IgG) and nucleoprotein IgG (N‐IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants (n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S‐IgG in 97% of subjects for at least 13 months after infection. Only 36% had N‐IgG by 13 months. The mean S‐IgG concentrations declined from 8 to 13 months by less than one third; N‐IgG concentrations declined by two‐thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs. Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV‐2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS‐CoV‐2 spike IgG (S‐IgG) and nucleoprotein IgG (N‐IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants ( n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S‐IgG in 97% of subjects for at least 13 months after infection. Only 36% had N‐IgG by 13 months. The mean S‐IgG concentrations declined from 8 to 13 months by less than one third; N‐IgG concentrations declined by two‐thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs. Most subjects develop antibodies to SARS‐CoV‐2 following infection. In order to estimate the duration of immunity induced by SARS‐CoV‐2 it is important to understand for how long antibodies persist after infection in humans. Here, we assessed the persistence of serum antibodies following WT SARS‐CoV‐2 infection at 8 and 13 months after diagnosis in 367 individuals. The SARS‐CoV‐2 spike IgG (S‐IgG) and nucleoprotein IgG (N‐IgG) concentrations and the proportion of subjects with neutralizing antibodies (NAb) were assessed. Moreover, the NAb titers among a smaller subset of participants ( n = 78) against a WT virus (B) and variants of concern (VOCs): Alpha (B.1.1.7), Beta (B.1.351), and Delta (B.1.617.2) were determined. We found that NAb against the WT virus persisted in 89% and S‐IgG in 97% of subjects for at least 13 months after infection. Only 36% had N‐IgG by 13 months. The mean S‐IgG concentrations declined from 8 to 13 months by less than one third; N‐IgG concentrations declined by two‐thirds. Subjects with severe infection had markedly higher IgG and NAb levels and are expected to remain seropositive for longer. Significantly lower NAb titers against the variants compared to the WT virus, especially after a mild disease, suggests reduced protection against VOCs. A year after WT SARS‐CoV‐2 infection high seropositivity rate was observed: 89% of subjects had persisting neutralizing antibodies and up to 97% had anti‐spike IgG antibodies. Compared to the WT virus, neutralizing antibody titers were reduced for variants of concern Alpha, Beta, and Delta. |
Author | Isosaari, Elina Haveri, Anu Österlund, Pamela Virta, Camilla Nohynek, Hanna Ekström, Nina Melin, Merit Solastie, Anna Palmu, Arto A |
AuthorAffiliation | 1 Department of Health Security Finnish Institute for Health and Welfare Helsinki Finland 2 Department of Public Health and Welfare Finnish Institute for Health and Welfare Helsinki Finland |
AuthorAffiliation_xml | – name: 2 Department of Public Health and Welfare Finnish Institute for Health and Welfare Helsinki Finland – name: 1 Department of Health Security Finnish Institute for Health and Welfare Helsinki Finland |
Author_xml | – sequence: 1 givenname: Anu orcidid: 0000-0003-4620-7536 surname: Haveri fullname: Haveri, Anu email: anu.haveri@thl.fi organization: Finnish Institute for Health and Welfare – sequence: 2 givenname: Nina orcidid: 0000-0003-2220-9027 surname: Ekström fullname: Ekström, Nina email: nina.ekstrom@thl.fi organization: Finnish Institute for Health and Welfare – sequence: 3 givenname: Anna surname: Solastie fullname: Solastie, Anna organization: Finnish Institute for Health and Welfare – sequence: 4 givenname: Camilla surname: Virta fullname: Virta, Camilla organization: Finnish Institute for Health and Welfare – sequence: 5 givenname: Pamela surname: Österlund fullname: Österlund, Pamela organization: Finnish Institute for Health and Welfare – sequence: 6 givenname: Elina surname: Isosaari fullname: Isosaari, Elina organization: Finnish Institute for Health and Welfare – sequence: 7 givenname: Hanna surname: Nohynek fullname: Nohynek, Hanna organization: Finnish Institute for Health and Welfare – sequence: 8 givenname: Arto A surname: Palmu fullname: Palmu, Arto A organization: Finnish Institute for Health and Welfare – sequence: 9 givenname: Merit surname: Melin fullname: Melin, Merit organization: Finnish Institute for Health and Welfare |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34580856$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1007/s00508‐021‐01922‐y 10.1038/s41467-021-24285-4 10.1002/eji.202048970 10.1056/NEJMc2100362 10.1080/22221751.2020.1780951 10.1126/sciimmunol.abe0367 10.1038/s41564-020-00813-8 10.1084/jem.20202515 10.1016/S0140-6736(21)01290-3 10.1089/vim.2020.0321 10.1126/science.abd7728 10.1126/science.abc6284 10.1038/s41586-021-03207-w 10.1128/JVI.01828-20 10.1038/s41467-020-16256-y 10.3390/vaccines9050517 10.1038/s41467-021-22351-5 10.1101/2021.07.28.21260990 10.1038/s41591‐021‐01377‐8 10.1038/s41586‐021‐03696‐9 10.1056/NEJMoa2022483 10.1038/s41586-020-2380-z 10.1128/JCM.02107-20 10.1016/j.lanepe.2021.100150 10.1001/jama.2020.27124 10.1038/s41586-021-03647-4 10.1056/NEJMc2103740 10.1016/j.cell.2021.03.036 10.1126/sciimmunol.abj1750 10.1056/NEJMc2107799 10.1126/scitranslmed.abd2223 10.1038/s41598-021-81862-9 10.1038/s41591-021-01318-5 10.1038/s41586-021-03693-y 10.1038/s41467-021-21111-9 10.1016/S0140-6736(21)00675-9 10.1038/s41586-020-03041-6 10.1056/NEJMc2103916 10.1038/s41586-021-03777-9 10.1056/NEJMoa2027906 10.1093/infdis/jiab127 10.1016/j.trsl.2021.02.006 10.1101/2021.06.23.21259327 10.1126/science.abf4063 10.1056/NEJMoa2028436 10.1128/mBio.00902-21 10.1093/cid/ciab607 10.1093/infdis/jiab255 10.2807/1560-7917.ES.2020.25.11.2000266 10.1101/2021.06.05.447177 10.3346/jkms.2021.36.e157 10.1093/cid/ciab004 |
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References_xml | – volume: 5 start-page: 1598 year: 2020 end-page: 1607 article-title: Longitudinal observation and decline of neutralizing antibody responses in the three months following SARS‐CoV‐2 infection in humans publication-title: Nat. Microbiol. – volume: 595 start-page: 421 year: 2021 end-page: 425 article-title: SARS‐CoV‐2 infection induces long‐lived bone marrow plasma cells in humans publication-title: Nature – year: 2021 article-title: Long‐term persistence of spike antibody and predictive modeling of antibody dynamics following infection with SARS‐CoV‐2 publication-title: Clin. Infect. Dis. – volume: 6 year: 2021 article-title: SARS‐CoV‐2 variants of concern partially escape humoral but not T‐cell responses in COVID‐19 convalescent donors and vaccinees publication-title: Sci Immunol – year: 2021 article-title: Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS‐CoV‐2 infection publication-title: Nat. Med. – volume: 584 start-page: 115 year: 2020 end-page: 119 article-title: Human neutralizing antibodies elicited by SARS‐CoV‐2 infection publication-title: Nature – volume: 34 start-page: 201 year: 2021 end-page: 209 article-title: Antibody (IgA, IgG, and IgG Subtype) Responses to SARS‐CoV‐2 in Severe and Nonsevere COVID‐19 Patients publication-title: Viral Immunol. – volume: 325 start-page: 529 year: 2021 end-page: 531 article-title: Genetic variants of SARS‐CoV‐2‐what do they mean? publication-title: JAMA – year: 2021 article-title: Persistence of Antibody and Cellular Immune Responses in COVID‐19 patients over Nine Months after Infection publication-title: J. Infect. Dis. – volume: 13 year: 2021 article-title: IgA dominates the early neutralizing antibody response to SARS‐CoV‐2 publication-title: Sci. Transl. Med. – volume: 9 start-page: 1497 year: 2020 end-page: 1505 article-title: Serological differentiation between COVID‐19 and SARS infections publication-title: Emerg Microbes Infect – volume: 596 start-page: 276 year: 2021 end-page: 280 article-title: Reduced sensitivity of SARS‐CoV‐2 variant Delta to antibody neutralization publication-title: Nature – volume: 383 start-page: 2427 year: 2020 end-page: 2438 article-title: Safety and immunogenicity of SARS‐CoV‐2 mRNA‐1273 vaccine in older adults publication-title: N. Engl. J. Med. – volume: 2 start-page: 313 year: 2021 end-page: 320.e4 article-title: Stable neutralizing antibody levels 6 months after mild and severe COVID‐19 episodes publication-title: Med (N Y) – start-page: 1 year: 2021 end-page: 11 article-title: Safety and immunogenicity of an mRNA‐lipid nanoparticle vaccine candidate against SARS‐CoV‐2 : A phase 1 randomized clinical trial publication-title: Wien Klin Wochenschr – volume: 184 start-page: 2384 year: 2021 end-page: 2393.e12 article-title: SARS‐CoV‐2 variants B.1.351 and P.1 escape from neutralizing antibodies publication-title: Cell – volume: 7 year: 2021 article-title: Decreased infectivity following BNT162b2 vaccination: A prospective cohort study in Israel publication-title: Lancet Reg Health Eur – volume: 12 start-page: 844 year: 2021 end-page: 849 article-title: Rapid decline of neutralizing antibodies against SARS‐CoV‐2 among infected healthcare workers publication-title: Nat. Commun. – volume: 383 start-page: 2439 year: 2020 end-page: 2450 article-title: Safety and immunogenicity of two RNA‐based Covid‐19 vaccine candidates publication-title: N. Engl. J. Med. – volume: 384 start-page: 1866 year: 2021 end-page: 1868 article-title: New SARS‐CoV‐2 variants ‐ clinical, public health, and vaccine implications publication-title: N. Engl. J. Med. – volume: 383 start-page: 1920 year: 2020 end-page: 1931 article-title: An mRNA vaccine against SARS‐CoV‐2 ‐ Preliminary report publication-title: N. Engl. J. Med. – year: 2021 article-title: Neutralization against B.1.351 and B.1.617.2 with sera of COVID‐19 recovered cases and vaccinees of BBV152 publication-title: bioRxiv – volume: 385 start-page: 664 year: 2021 end-page: 666 article-title: Infection and vaccine‐induced neutralizing‐antibody responses to the SARS‐CoV‐2 B.1.617 variants publication-title: N. Engl. J. Med. – year: 2021 article-title: Sex differences in the evolution of neutralizing antibodies to SARS‐CoV‐2 publication-title: J. Infect. Dis. – volume: 36 year: 2021 article-title: Antibody responses one year after mild SARS‐CoV‐2 infection publication-title: J. Korean Med. Sci. – volume: 369 start-page: 806 year: 2020 end-page: 811 article-title: DNA vaccine protection against SARS‐CoV‐2 in rhesus macaques publication-title: Science – volume: 11 start-page: 2608 year: 2021 end-page: 2609 article-title: SARS‐CoV‐2 infection elicits a rapid neutralizing antibody response that correlates with disease severity publication-title: Sci. Rep. – volume: 12 start-page: 2117 year: 2021 end-page: 2115 article-title: Seroprevalence and correlates of SARS‐CoV‐2 neutralizing antibodies from a population‐based study in Bonn, Germany publication-title: Nat. Commun. – volume: 590 start-page: 630 year: 2021 end-page: 634 article-title: Correlates of protection against SARS‐CoV‐2 in rhesus macaques publication-title: Nature – volume: 591 start-page: 639 year: 2021 end-page: 644 article-title: Evolution of antibody immunity to SARS‐CoV‐2 publication-title: Nature – volume: 50 start-page: 2025 year: 2020 end-page: 2040 article-title: Seroprevalence of anti‐SARS‐CoV‐2 antibodies in COVID‐19 patients and healthy volunteers up to 6 months post disease onset publication-title: Eur. J. Immunol. – volume: 384 start-page: 2352 year: 2021 end-page: 2354 article-title: Neutralization of SARS‐CoV‐2 variants B.1.429 and B.1.351 publication-title: N. Engl. J. Med. – volume: 397 start-page: 1459 year: 2021 end-page: 1469 article-title: SARS‐CoV‐2 infection rates of antibody‐positive compared with antibody‐negative health‐care workers in England: a large, multicentre, prospective cohort study (SIREN) publication-title: Lancet – volume: 95 start-page: e01828 year: 2021 end-page: 20 article-title: Changes in SARS‐CoV‐2 Spike versus Nucleoprotein Antibody Responses Impact the Estimates of Infections in Population‐Based Seroprevalence Studies publication-title: J. Virol. – volume: 397 start-page: 2331 year: 2021 end-page: 2333 article-title: Neutralising antibody activity against SARS‐CoV‐2 VOCs B.1.617.2 and B.1.351 by BNT162b2 vaccination publication-title: Lancet – volume: 11 start-page: 2251 year: 2020 article-title: A human monoclonal antibody blocking SARS‐CoV‐2 infection publication-title: Nat. Commun. – volume: 9 year: 2021 article-title: Neutralizing antibody response of vaccinees to SARS‐CoV‐2 variants publication-title: Vaccines (Basel) – volume: 25 year: 2020 article-title: Serological and molecular findings during SARS‐CoV‐2 infection: the first case study in Finland, January to February 2020 publication-title: Euro Surveill – volume: 73 start-page: e699 year: 2021 end-page: e709 article-title: The duration, dynamics and determinants of SARS‐CoV‐2 antibody responses in individual healthcare workers publication-title: Clin. Infect. Dis. – volume: 5 year: 2020 article-title: Persistence and decay of human antibody responses to the receptor binding domain of SARS‐CoV‐2 spike protein in COVID‐19 patients publication-title: Sci Immunol – volume: 232 start-page: 60 year: 2021 end-page: 74 article-title: Immunogenicity and crossreactivity of antibodies to the nucleocapsid protein of SARS‐CoV‐2: utility and limitations in seroprevalence and immunity studies publication-title: Transl. Res. – volume: 384 start-page: 2259 year: 2021 end-page: 2261 article-title: Antibody Persistence through 6 Months after the Second Dose of mRNA‐1273 Vaccine for Covid‐19 publication-title: N. Engl. J. Med. – volume: 218 year: 2021 article-title: Persistent cellular immunity to SARS‐CoV‐2 infection publication-title: J. Exp. Med. – volume: 27 start-page: 917 year: 2021 end-page: 924 article-title: Sensitivity of infectious SARS‐CoV‐2 B.1.1.7 and B.1.351 variants to neutralizing antibodies publication-title: Nat. Med. – volume: 12 start-page: e00902 year: 2021 end-page: 21 article-title: A generic, scalable, and rapid time‐resolved förster resonance energy transfer‐based assay for antigen detection‐SARS‐CoV‐2 as a proof of concept publication-title: mBio – volume: 370 start-page: 1227 year: 2020 end-page: 1230 article-title: Robust neutralizing antibodies to SARS‐CoV‐2 infection persist for months publication-title: Science – year: 2021 article-title: Naturally enhanced neutralizing breadth against SARS‐CoV‐2 one year after infection publication-title: Nature – volume: 371 year: 2021 article-title: Immunological memory to SARS‐CoV‐2 assessed for up to 8 months after infection publication-title: Science – year: 2021 article-title: Reduced neutralisation of the Delta (B.1.617.2) SARS‐CoV‐2 variant of concern following vaccination publication-title: medRxiv – volume: 12 start-page: 3991 year: 2021 end-page: 3994 article-title: COVID‐19 mRNA vaccine induced antibody responses against three SARS‐CoV‐2 variants publication-title: Nat. Commun. – year: 2020 – volume: 58 start-page: e02107 year: 2020 end-page: 20 article-title: Neutralizing antibodies correlate with protection from SARS‐CoV‐2 in humans during a fishery vessel outbreak with a high attack rate publication-title: J Clin Microbiol – year: 2021 article-title: Analytical and clinical evaluation of antibody tests for SARS‐CoV‐2 serosurveillance studies used in Finland in 2020 publication-title: medRxiv – year: 2021 article-title: A highly sensitive and specific SARS‐CoV‐2 spike‐ and nucleoprotein‐based fluorescent multiplex immunoassay (FMIA) to measure IgG, IgA and IgM class antibodies publication-title: medRxiv – volume: 596 start-page: 273 year: 2021 end-page: 275 article-title: BNT162b2‐elicited neutralization of B.1.617 and other SARS‐CoV‐2 variants publication-title: Nature – ident: e_1_2_10_49_1 doi: 10.1007/s00508‐021‐01922‐y – ident: e_1_2_10_24_1 doi: 10.1038/s41467-021-24285-4 – ident: e_1_2_10_6_1 doi: 10.1002/eji.202048970 – ident: e_1_2_10_21_1 doi: 10.1056/NEJMc2100362 – ident: e_1_2_10_36_1 doi: 10.1080/22221751.2020.1780951 – ident: e_1_2_10_17_1 doi: 10.1126/sciimmunol.abe0367 – ident: e_1_2_10_19_1 doi: 10.1038/s41564-020-00813-8 – ident: e_1_2_10_35_1 doi: 10.1084/jem.20202515 – ident: e_1_2_10_42_1 doi: 10.1016/S0140-6736(21)01290-3 – ident: e_1_2_10_15_1 doi: 10.1089/vim.2020.0321 – ident: e_1_2_10_2_1 doi: 10.1126/science.abd7728 – ident: e_1_2_10_29_1 doi: 10.1126/science.abc6284 – ident: e_1_2_10_8_1 doi: 10.1038/s41586-021-03207-w – ident: e_1_2_10_37_1 doi: 10.1128/JVI.01828-20 – ident: e_1_2_10_3_1 doi: 10.1038/s41467-020-16256-y – ident: e_1_2_10_22_1 doi: 10.3390/vaccines9050517 – ident: e_1_2_10_39_1 doi: 10.1038/s41467-021-22351-5 – ident: e_1_2_10_56_1 doi: 10.1101/2021.07.28.21260990 – ident: e_1_2_10_5_1 doi: 10.1038/s41591‐021‐01377‐8 – ident: e_1_2_10_13_1 doi: 10.1038/s41586‐021‐03696‐9 – ident: e_1_2_10_48_1 doi: 10.1056/NEJMoa2022483 – ident: e_1_2_10_4_1 doi: 10.1038/s41586-020-2380-z – ident: e_1_2_10_27_1 doi: 10.1128/JCM.02107-20 – ident: e_1_2_10_31_1 doi: 10.1016/j.lanepe.2021.100150 – ident: e_1_2_10_20_1 doi: 10.1001/jama.2020.27124 – ident: e_1_2_10_34_1 doi: 10.1038/s41586-021-03647-4 – ident: e_1_2_10_40_1 doi: 10.1056/NEJMc2103740 – ident: e_1_2_10_41_1 doi: 10.1016/j.cell.2021.03.036 – ident: e_1_2_10_23_1 doi: 10.1126/sciimmunol.abj1750 – ident: e_1_2_10_25_1 doi: 10.1056/NEJMc2107799 – ident: e_1_2_10_16_1 doi: 10.1126/scitranslmed.abd2223 – ident: e_1_2_10_32_1 doi: 10.1038/s41598-021-81862-9 – ident: e_1_2_10_14_1 doi: 10.1038/s41591-021-01318-5 – ident: e_1_2_10_45_1 doi: 10.1038/s41586-021-03693-y – ident: e_1_2_10_18_1 doi: 10.1038/s41467-021-21111-9 – ident: e_1_2_10_28_1 doi: 10.1016/S0140-6736(21)00675-9 – ident: e_1_2_10_30_1 doi: 10.1038/s41586-020-03041-6 – ident: e_1_2_10_51_1 doi: 10.1056/NEJMc2103916 – ident: e_1_2_10_26_1 doi: 10.1038/s41586-021-03777-9 – ident: e_1_2_10_47_1 doi: 10.1056/NEJMoa2027906 – ident: e_1_2_10_11_1 doi: 10.1093/infdis/jiab127 – ident: e_1_2_10_38_1 doi: 10.1016/j.trsl.2021.02.006 – ident: e_1_2_10_44_1 doi: 10.1101/2021.06.23.21259327 – ident: e_1_2_10_54_1 – ident: e_1_2_10_9_1 doi: 10.1126/science.abf4063 – ident: e_1_2_10_46_1 doi: 10.1056/NEJMoa2028436 – ident: e_1_2_10_55_1 doi: 10.1128/mBio.00902-21 – ident: e_1_2_10_33_1 doi: 10.1093/cid/ciab607 – volume: 2 start-page: 313 year: 2021 ident: e_1_2_10_7_1 article-title: Stable neutralizing antibody levels 6 months after mild and severe COVID‐19 episodes publication-title: Med (N Y) – ident: e_1_2_10_10_1 doi: 10.1093/infdis/jiab255 – ident: e_1_2_10_52_1 doi: 10.2807/1560-7917.ES.2020.25.11.2000266 – ident: e_1_2_10_43_1 doi: 10.1101/2021.06.05.447177 – year: 2021 ident: e_1_2_10_53_1 article-title: Analytical and clinical evaluation of antibody tests for SARS‐CoV‐2 serosurveillance studies used in Finland in 2020 publication-title: medRxiv – ident: e_1_2_10_12_1 doi: 10.3346/jkms.2021.36.e157 – ident: e_1_2_10_50_1 doi: 10.1093/cid/ciab004 |
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SubjectTerms | Adolescent Adult Aged Antibodies Antibodies, Neutralizing - metabolism Antibodies, Viral - metabolism Clinical Cohort Studies Coronavirus Nucleocapsid Proteins - immunology COVID-19 - epidemiology COVID-19 - immunology Female Finland - epidemiology Humans IgG antibodies Immunity to infection Immunoglobulin G Immunoglobulin G - metabolism Infections Male Middle Aged neutralizing antibodies SARS-CoV-2 - physiology SARS‐CoV‐2 Seroepidemiologic Studies seroprevalence Severe acute respiratory syndrome coronavirus 2 Spike Glycoprotein, Coronavirus - immunology Time Factors variants of concern Viruses Young Adult |
Title | Persistence of neutralizing antibodies a year after SARS‐CoV‐2 infection in humans |
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