Evidence map›Paper›PMID 33984048›Full record

ArticlePloS one2021

SARS-CoV-2 antibody immunoassays in serial samples reveal earlier seroconversion in acutely ill COVID-19 patients developing ARDS.

Marie-Luise Buchholtz, Florian M Arend, Peter Eichhorn, Michael Weigand, Alisa Kleinhempel, Kurt Häusler, Mathias Bruegel, Lesca M Holdt, Daniel Teupser

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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.

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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Marie-Luise BuchholtzInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Florian M ArendInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Peter EichhornInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Michael WeigandInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Alisa KleinhempelInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Kurt HäuslerInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Mathias BruegelInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Lesca M HoldtInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Daniel TeupserInstitute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0001-9843-0145
LMU Klinikum · DE

Funding

RETINAL MECHANISMS IN VISIONR01EY001711 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MACLEOD, DONALD I · 1985 to 2011
$3.2M
NEI NIH HHS R01 EY001711
6 · The paper itself

Abstract

objectivesDuring the COVID-19 pandemic, SARS-CoV-2 antibody testing has been suggested for (1) screening populations for disease prevalence, (2) diagnostics, and (3) guiding therapeutic applications. Here, we conducted a detailed clinical evaluation of four Anti-SARS-CoV-2 immunoassays in samples from acutely ill COVID-19 patients and in two negative cohorts.

methods443 serum specimens from serial sampling of 29 COVID-19 patients were used to determine clinical sensitivities. Patients were stratified for the presence of acute respiratory distress syndrome (ARDS). Individual serum specimens from a pre-COVID-19 cohort of 238 healthy subjects and from a PCR-negative clinical cohort of 257 patients were used to determine clinical specificities. All samples were measured side-by-side with the Anti-SARS-CoV-2-ELISA (IgG), Anti-SARS-CoV-2-ELISA (IgA) and Anti-SARS-CoV-2-NCP-ELISA (IgG) (Euroimmun AG, Lübeck, Germany) and the Elecsys Anti-SARS-CoV-2 ECLIA (Roche Diagnostics International, Rotkreuz, Switzerland).

resultsMedian seroconversion occurred earlier in ARDS patients (8-9 days) than in non-ARDS patients (11-17 days), except for EUR N-IgG. Rates of positivity and mean signal ratios in the ARDS group were significantly higher than in the non-ARDS group. Sensitivities between the four tested immunoassays were equivalent. In the set of negative samples, the specificity of the Anti-SARS-CoV-2-ELISA (IgA) was lower (93.9%) compared to all other assays (≥98.8%) and the specificity of Anti-SARS-CoV-2-NCP-ELISA (IgG) was lower (98.8%) than that of Elecsys Anti-SARS-CoV-2 (100%).

conclusionsSerial sampling in COVID-19 patients revealed earlier seroconversion and higher signal ratios of SARS-CoV-2 antibodies as a potential risk marker for the development of ARDS, suggesting a utility for antibody testing in acutely diseased patients.

Indexed as

SeroconversionAdultAgedAged, 80 and overAntibodies, ViralCOVID-19COVID-19 Serological TestingFemaleHumansImmunoassayImmunoglobulin GMaleMiddle AgedRespiratory Distress SyndromeSARS-CoV-2Antibodies, ViralImmunoglobulin G

Identifiers

PMID33984048
PMCPMC8118560
OpenAlexW3133247579

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.