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 inEuropean journal of immunology Vol. 51; no. 12; pp. 3202 - 3213
Main Authors Haveri, Anu, Ekström, Nina, Solastie, Anna, Virta, Camilla, Österlund, Pamela, Isosaari, Elina, Nohynek, Hanna, Palmu, Arto A, Melin, Merit
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.12.2021
John Wiley and Sons Inc
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Online AccessGet full text
ISSN0014-2980
1521-4141
1521-4141
DOI10.1002/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.
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
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  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
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  surname: Solastie
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  organization: Finnish Institute for Health and Welfare
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  surname: Palmu
  fullname: Palmu, Arto A
  organization: Finnish Institute for Health and Welfare
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  surname: Melin
  fullname: Melin, Merit
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/34580856$$D View this record in MEDLINE/PubMed
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Issue 12
Keywords IgG antibodies
seroprevalence
neutralizing antibodies
SARS-CoV-2
variants of concern
Language English
License Attribution
2021 The Authors. European Journal of Immunology published by Wiley-VCH GmbH.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Snippet 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...
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...
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StartPage 3202
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Feji.202149535
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https://pubmed.ncbi.nlm.nih.gov/PMC8646652
Volume 51
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