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SARS-CoV-2 induces a durable and antigen specific humoral immunity after asymptomatic to mild COVID-19 infection
Sebastian Havervall; August Jernbom Falk; Jonas Klingstrom; Henry Ng; Nina Greilert Norin; Lena Gabrielsson; Ann-Christine Salomonsson; Eva Isaksson; Ann-Sofie Rudberg; Cecilia Hellstrom; Eni Andersson; Jennie Olofsson; Lovisa Skoglund; Jamil Yousef; Elisa Pin; Wanda Christ; Mikaela Olausson; My Hedhammar; Hanna Tegel; Sara Mangsbo; Mia Phillipson; Anna Manberg; Sophia Hober; Peter Nilsson; Charlotte Thalin.
Affiliation
  • Sebastian Havervall; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
  • August Jernbom Falk; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Jonas Klingstrom; Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden
  • Henry Ng; Department of Medical Cell Biology, Uppsala University, SciLifeLab, Uppsala, Sweden
  • Nina Greilert Norin; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
  • Lena Gabrielsson; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
  • Ann-Christine Salomonsson; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
  • Eva Isaksson; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
  • Ann-Sofie Rudberg; Department of Neurology, Danderyd Hospital, Stockholm, Sweden
  • Cecilia Hellstrom; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Eni Andersson; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Jennie Olofsson; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Lovisa Skoglund; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Jamil Yousef; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Elisa Pin; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Wanda Christ; Centre for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institute, Stockholm, Sweden
  • Mikaela Olausson; Department of Microbiology, Public Health Agency of Sweden, Solna, Sweden
  • My Hedhammar; Division of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden
  • Hanna Tegel; Division of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden
  • Sara Mangsbo; Department of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, Uppsala, Sweden
  • Mia Phillipson; Department of Medical Cell Biology, Uppsala University, SciLifeLab, Uppsala, Sweden
  • Anna Manberg; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Sophia Hober; Division of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden
  • Peter Nilsson; Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden
  • Charlotte Thalin; Department of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden
Preprint in English | medRxiv | ID: ppmedrxiv-21249162
Journal article
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ABSTRACT
Current SARS-CoV-2 serological assays generate discrepant results, and the longitudinal characteristics of antibodies targeting various antigens after asymptomatic to mild COVID-19 are yet to be established. This longitudinal cohort study including 1965 healthcare workers, of which 381 participants exhibited antibodies against the SARS-CoV-2 spike antigen at study inclusion, reveal that these antibodies remain detectable in most participants, 96%, at least four months post infection, despite having had no or mild symptoms. Virus neutralization capacity was confirmed by microneutralization assay in 91% of study participants at least four months post infection. Contrary to antibodies targeting the spike protein, antibodies against the nucleocapsid protein were only detected in 80% of previously anti-nucleocapsid IgG positive healthcare workers. Both anti-spike and anti-nucleocapsid IgG levels were significantly higher in previously hospitalized COVID-19 patients four months post infection than in healthcare workers four months post infection (p=2*10-23 and 2*10-13 respectively). Although the magnitude of humoral response was associated with disease severity, our findings support a durable and functional humoral response after SARS-CoV-2 infection even after no or mild symptoms. We further demonstrate differences in antibody kinetics depending on the antigen, arguing against the use of the nucleocapsid protein as target antigen in population-based SARS-CoV-2 serological surveys.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study Language: English Year: 2021 Document type: Preprint
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