Evidence map›Paper›PMID 35020778›Full record

ArticlePloS one2022

SARS-CoV-2 induces a durable and antigen specific humoral immunity after asymptomatic to mild COVID-19 infection.

Sebastian Havervall, August Jernbom Falk, Jonas Klingström, Henry Ng, Nina Greilert-Norin, Lena Gabrielsson, Ann-Christin Salomonsson, Eva Isaksson, Ann-Sofie Rudberg, Cecilia Hellström and 15 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06784739 (COMMUNITY - the COVID-19 Immunity Study), which is not on this map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06784739 recruitingnot on this map

COMMUNITY - the COVID-19 Immunity Study

TypeobservationalSponsorDanderyd HospitalRan2020 to 2027Enrolled5,500ConditionsCOVID 19, Respiratory Synctial Virus, Influenza Virus, SARS-CoV-2 VirusArmsBlood sampling, Mucosal sampling, PCR-test
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

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  12. Symptom Burden and Immune Dynamics 6 to 18 Months Following Mild Severe Acute Respiratory Syndrome Coronavirus 2 Infection (SARS-CoV-2): A Case-control Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 1 country.

Sebastian HavervallDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
August Jernbom FalkDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0002-7773-1851
Jonas KlingströmCentre for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0001-9076-1441
Henry NgDepartment of Medical Cell Biology, Uppsala University, SciLifeLab, Uppsala, Sweden.ORCID 0000-0003-2873-9088
Nina Greilert-NorinDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
Lena GabrielssonDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
Ann-Christin SalomonssonDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
Eva IsakssonDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.ORCID 0000-0003-0289-8750
Ann-Sofie RudbergDepartment of Neurology, Danderyd Hospital, Stockholm, Sweden.
Cecilia HellströmDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0003-0880-5375
Eni AnderssonDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0002-5115-0637
Jennie OlofssonDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.
Lovisa SkoglundDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.
Jamil YousefDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0001-5915-1258
Elisa PinDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.
Wanda ChristCentre for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0003-3886-5248
Mikaela OlaussonDepartment of Microbiology, Public Health Agency of Sweden, Solna, Sweden.
My HedhammarDivision of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden.
Hanna TegelDivision of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden.
Sara MangsboDepartment of Pharmaceutical Biosciences, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Mia PhillipsonDepartment of Medical Cell Biology, Uppsala University, SciLifeLab, Uppsala, Sweden.
Anna MånbergDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.
Sophia HoberDivision of Protein Technology, Department of Protein Science, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0003-0605-8417
Peter NilssonDivision of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0002-4657-8532
Charlotte ThålinDepartment of Clinical Sciences, Karolinska Institute, Danderyd Hospital, Stockholm, Sweden.
Science for Life Laboratory · SEKarolinska Institutet · SEKTH Royal Institute of Technology · SEUppsala University · SEPublic Health Agency of Sweden · SEDanderyds sjukhus · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Immunity, HumoralAdultAntibodies, NeutralizingAntibodies, ViralAsymptomatic InfectionsCOVID-19FemaleHealth PersonnelHumansImmunoglobulin GLongitudinal StudiesMaleMiddle AgedNucleocapsidSARS-CoV-2Severity of Illness IndexAntibodies, NeutralizingAntibodies, ViralImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID35020778
PMCPMC8754314
OpenAlexW4226064735

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.