Evidence map›Paper›PMID 34061367›Full record

ArticleJournal of medical virology2021

Longitudinal detection of SARS-CoV-2-specific antibody responses with different serological methods.

Petra Emmerich, Ronald von Possel, Christoph Josef Hemmer, Carlos Fritzsche, Hilte Geerdes-Fenge, Babett Menge, Claudia Messing, Viola Borchardt-Lohölter, Christina Deschermeier, Katja Steinhagen

Abstract readComparative Study
In one paragraph

Article in Journal of medical virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  14. Cancer Occurrence as the Upcoming Complications of COVID-19.Frontiers in molecular biosciences · 2021
    Review
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

10 authors.

Petra EmmerichDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, WHO Collaborating Center for Arbovirus and Hemorrhagic Fever Reference and Research, Hamburg, Germany.
Ronald von PosselDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, WHO Collaborating Center for Arbovirus and Hemorrhagic Fever Reference and Research, Hamburg, Germany.
Christoph Josef HemmerDepartment of Tropical Medicine and Infectious Diseases, Center for Internal Medicine, University of Rostock, Rostock, Germany.
Carlos FritzscheDepartment of Tropical Medicine and Infectious Diseases, Center for Internal Medicine, University of Rostock, Rostock, Germany.
Hilte Geerdes-FengeDepartment of Tropical Medicine and Infectious Diseases, Center for Internal Medicine, University of Rostock, Rostock, Germany.
Babett MengeInstitute for Experimental Immunology, Affiliated with EUROIMMUN Medizinische Labordiagnostika AG, Luebeck, Germany.
Claudia MessingInstitute for Experimental Immunology, Affiliated with EUROIMMUN Medizinische Labordiagnostika AG, Luebeck, Germany.
Viola Borchardt-LohölterInstitute for Experimental Immunology, Affiliated with EUROIMMUN Medizinische Labordiagnostika AG, Luebeck, Germany.
Christina DeschermeierDepartment for Infectious Disease Diagnostics, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Katja SteinhagenInstitute for Experimental Immunology, Affiliated with EUROIMMUN Medizinische Labordiagnostika AG, Luebeck, Germany.

Funding

Bundesministerium für Bildung und Forschung 01KI20210
6 · The paper itself

Abstract

Serological testing for anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies is used to detect ongoing or past SARS-CoV-2 infections. To study the kinetics of anti-SARS-CoV-2 antibodies and to assess the diagnostic performances of eight serological assays, we used 129 serum samples collected on known days post symptom onset (dpso) from 42 patients with polymerase chain reaction-confirmed coronavirus disease 2019 (COVID-19) and 54 serum samples from healthy blood donors, and children infected with seasonal coronaviruses. The sera were analyzed for the presence of immunoglobulin G (IgG), immunoglobulin M (IgM), and immunoglobulin A (IgA) antibodies using indirect immunofluorescence testing (IIFT) based on SARS-CoV-2-infected cells. They were further tested for antibodies against the S1 domain of the SARS-CoV-2 spike protein (IgG, IgA) and against the viral nucleocapsid protein (IgG, IgM) using enzyme-linked immunosorbent assays. The assay specificities were 94.4%-100%. The sensitivities varied largely between assays, reflecting their respective purposes. The sensitivities of IgA and IgM assays were the highest between 11 and 20 dpso, whereas the sensitivities of IgG assays peaked between 20 and 60 dpso. IIFT showed the highest sensitivities due to the use of the whole SARS-CoV-2 as substrate and provided information on whether or not the individual has been infected with SARS-CoV-2. Enzyme-linked immunosorbent assays provided further information about both the prevalence and concentration of specific antibodies against selected antigens of SARS-CoV-2.

Indexed as

COVID-19 Serological TestingAdultAgedAged, 80 and overAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19Enzyme-Linked Immunosorbent AssayFemaleFluorescent Antibody Technique, IndirectHumansImmunoglobulin IsotypesKineticsMaleMiddle AgedPhosphoproteinsAntibodies, ViralCoronavirus Nucleocapsid ProteinsImmunoglobulin Isotypesnucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibodiesCOVID-19ELISAimmunofluorescenceSARS-CoV-2serology

Identifiers

PMID34061367
PMCPMC8242665

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.