Evidence map›Paper›PMID 35493512›Full record

ArticleFrontiers in immunology2022

High Titers of Low Affinity Antibodies in COVID-19 Patients Are Associated With Disease Severity.

Jan Hendriks, Richard Schasfoort, Michelle Koerselman, Maureen Dannenberg, Alexander Daniel Cornet, Albertus Beishuizen, Job van der Palen, Johannes Krabbe, Alide H L Mulder, Marcel Karperien

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Cross-reactive humoral and CD4Frontiers in immunology · 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

10 authors at 3 institutions in 1 country.

Jan HendriksDepartment of Developmental BioEngineering, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Richard SchasfoortDepartment of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Michelle KoerselmanDepartment of Developmental BioEngineering, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Maureen DannenbergDepartment of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Alexander Daniel CornetIntensive Care Center, Medisch Spectrum Twente, Enschede, Netherlands.
Albertus BeishuizenIntensive Care Center, Medisch Spectrum Twente, Enschede, Netherlands.
Job van der PalenMedical School, Medisch Spectrum Twente, Enschede, Netherlands.
Johannes KrabbeDepartment of Clinical Chemistry, Medlon BV, Enschede, Netherlands.
Alide H L MulderDepartment of Clinical Chemistry, Medlon BV, Enschede, Netherlands.
Marcel KarperienDepartment of Developmental BioEngineering, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
University of Twente · NLMedisch Spectrum Twente · NLZiekenhuis Groep Twente · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Almost 2 years from the beginning of the coronavirus disease 2019 (COVID-19) pandemic, there is still a lot unknown how the humoral response affects disease progression. In this study, we investigated humoral antibody responses against specific SARS-CoV2 proteins, their strength of binding, and their relationship with COVID severity and clinical information. Furthermore, we studied the interactions of the specific receptor-binding domain (RBD) in more depth by characterizing specific antibody response to a peptide library. Materials and Methods: We measured specific antibodies of isotypes IgM, IgG, and IgA, as well as their binding strength against the SARS-CoV2 antigens RBD, NCP, S1, and S1S2 in sera of 76 COVID-19 patients using surface plasmon resonance imaging. In addition, these samples were analyzed using a peptide epitope mapping assay, which consists of a library of peptides originating from the RBD. Results: A positive association was observed between disease severity and IgG antibody titers against all SARS-CoV2 proteins and additionally for IgM and IgA antibodies directed against RBD. Interestingly, in contrast to the titer of antibodies, the binding strength went down with increasing disease severity. Within the critically ill patient group, a positive association with pulmonary embolism, d-dimer, and antibody titers was observed. Conclusion: In critically ill patients, antibody production is high, but affinity is low, and maturation is impaired. This may play a role in disease exacerbation and could be valuable as a prognostic marker for predicting severity.

Indexed as

COVID-19Critical IllnessHumansImmunoglobulin AImmunoglobulin MRNA, ViralSARS-CoV-2Severity of Illness IndexImmunoglobulin AImmunoglobulin MRNA, ViralantibodiesCOVID-19immunoassayinfectious diseasesSPRi (surface plasmon resonance imagery)viral infection

Identifiers

PMID35493512
PMCPMC9043688
OpenAlexW4223946412

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.