Evidence map›Paper›PMID 36895570›Full record

ArticleFrontiers in immunology2023

Complementarity determining regions in SARS-CoV-2 hybrid immunity.

Glynis Frans, Doreen Dillaerts, Tom Dehaemers, Jan Van Elslande, Jonas De Leeuw, Lise Boon, Wim Maes, Nico Callewaert, Bas Calcoen, Lina Ancheva and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

17 authors at 3 institutions in 1 country.

Glynis FransDepartment of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.
Doreen DillaertsClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Tom DehaemersClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Jan Van ElslandeDepartment of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.
Jonas De LeeuwClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Lise BoonClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Wim MaesPharmAbs: The KU Leuven Antibody Center, KU Leuven, Leuven, Belgium.
Nico CallewaertClinical Laboratory, AZ Groeninge Hospital, Kortrijk, Belgium.
Bas CalcoenLaboratory for Thrombosis Research, KU Leuven Kulak Kortrijk, Kortrijk, Belgium.
Lina AnchevaClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Maaike CockxClinical and Diagnostic Immunology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Nick GeukensPharmAbs: The KU Leuven Antibody Center, KU Leuven, Leuven, Belgium.
Kusay AratSyBioMa, KU Leuven, Leuven, Belgium.
Rita DeruaSyBioMa, KU Leuven, Leuven, Belgium.
Pieter VermeerschDepartment of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.
Sebastien Christian CarpentierSyBioMa, KU Leuven, Leuven, Belgium.
Xavier BossuytDepartment of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.
KU Leuven · BEAZ Groeninge · BEResearch Institute for Chromatography · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pre-vaccination SARS-CoV-2 infection can boost protection elicited by COVID-19 vaccination and post-vaccination breakthrough SARS-CoV-2 infection can boost existing immunity conferred by COVID-19 vaccination. Such 'hybrid immunity' is effective against SARS-CoV-2 variants. In order to understand 'hybrid immunity' at the molecular level we studied the complementarity determining regions (CDR) of anti-RBD (receptor binding domain) antibodies isolated from individuals with 'hybrid immunity' as well as from 'naive' (not SARS-CoV-2 infected) vaccinated individuals. CDR analysis was done by liquid chromatography/mass spectrometry-mass spectrometry. Principal component analysis and partial least square differential analysis showed that COVID-19 vaccinated people share CDR profiles and that pre-vaccination SARS-CoV-2 infection or breakthrough infection further shape the CDR profile, with a CDR profile in hybrid immunity that clustered away from the CDR profile in vaccinated people without infection. Thus, our results show a CDR profile in hybrid immunity that is distinct from the vaccination-induced CDR profile.

Indexed as

COVID-19SARS-CoV-2Complementarity Determining RegionsCOVID-19 VaccinesHumansComplementarity Determining RegionsCOVID-19 Vaccinescomplementary determining regionCOVID-19hybrid immunitySARS-CoV-2vaccination

Identifiers

PMID36895570
PMCPMC9990870
OpenAlexW4321458424

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.