Evidence map›Paper›PMID 35603265›Full record

ArticleCommunications medicine2022

A rapid antibody screening haemagglutination test for predicting immunity to SARS-CoV-2 variants of concern.

Nina Urke Ertesvåg, Julie Xiao, Fan Zhou, Sonja Ljostveit, Helene Sandnes, Sarah Lartey, Marianne Sævik, Lena Hansen, Anders Madsen, Kristin G I Mohn and 21 more

Open access · goldAbstract read
In one paragraph

Article in Communications medicine, 2022. 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 28% 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, 8 citations in OpenAlex.

  1. Article
  2. Cross-reactive humoral and CD4Frontiers in immunology · 2023
    Article
  3. 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

31 authors at 9 institutions in 2 countries.

Nina Urke Ertesvåg *Influenza Centre, University of Bergen, Bergen, Norway.ORCID 0000-0001-5243-9101
Julie Xiao *MRC Human Immunology Unit, MRC Weatherall Institute, John Radcliffe Hospital, Oxford, UK.
Fan ZhouInfluenza Centre, University of Bergen, Bergen, Norway.ORCID 0000-0001-9918-3422
Sonja LjostveitInfluenza Centre, University of Bergen, Bergen, Norway.
Helene SandnesDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Sarah LarteyInfluenza Centre, University of Bergen, Bergen, Norway.
Marianne SævikDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-4670-4957
Lena HansenInfluenza Centre, University of Bergen, Bergen, Norway.
Anders MadsenInfluenza Centre, University of Bergen, Bergen, Norway.
Kristin G I MohnInfluenza Centre, University of Bergen, Bergen, Norway.ORCID 0000-0002-3249-1719
Elisabeth FjelltveitInfluenza Centre, University of Bergen, Bergen, Norway.
Jan Stefan OlofssonInfluenza Centre, University of Bergen, Bergen, Norway.ORCID 0000-0002-9772-4923
Tiong Kit TanMRC Human Immunology Unit, MRC Weatherall Institute, John Radcliffe Hospital, Oxford, UK.ORCID 0000-0001-8746-8308
Pramila RijalMRC Human Immunology Unit, MRC Weatherall Institute, John Radcliffe Hospital, Oxford, UK.ORCID 0000-0002-9214-9851
Lisa SchimanskiMRC Human Immunology Unit, MRC Weatherall Institute, John Radcliffe Hospital, Oxford, UK.
Siri ØyenEidsvåg Family Practice, Bergen, Norway.
Karl Albert BrokstadBroegelmann Research Laboratory, University of Bergen, Bergen, Norway.
Susanna DunachieOxford University Hospitals NHS Foundation Trust, Oxford, UK.ORCID 0000-0001-5665-6293
Anni JämsénNIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
William S JamesSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE UK.ORCID 0000-0002-2506-1198
Adam C HardingSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE UK.
Heli HarvalaMicrobiology Services, NHS Blood and Transplant, Colindale, UK.
Dung NguyenNuffield Department of Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, UK.
David RobertsClinical, Research and Development, NHS Blood and Transplant, Oxford, UK.
PHE Virology group
Maria ZambonVirology Reference Department, National Infection Service, Public Health England, Colindale, UK.ORCID 0000-0002-8897-7881
Oxford collaborative group
Alain Townsend *MRC Human Immunology Unit, MRC Weatherall Institute, John Radcliffe Hospital, Oxford, UK.
Bergen COVID-19 Research Group
Nina Langeland *Department of Clinical Science, University of Bergen, Bergen, Norway.ORCID 0000-0003-0278-1616
Rebecca Jane Cox *Influenza Centre, University of Bergen, Bergen, Norway.ORCID 0000-0002-8341-4078
Haukeland University Hospital · NOUniversity of Oxford · GBUniversity of Bergen · NOJohn Radcliffe Hospital · GBNHS Blood and Transplant · GBPublic Health England · GBMedawar Building for Pathogen Research · GBOxford University Hospitals NHS Trust · GBWestern Norway University of Applied Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Evaluation of susceptibility to emerging SARS-CoV-2 variants of concern (VOC) requires rapid screening tests for neutralising antibodies which provide protection. Methods: Firstly, we developed a receptor-binding domain-specific haemagglutination test (HAT) to Wuhan and VOC (alpha, beta, gamma and delta) and compared to pseudotype, microneutralisation and virus neutralisation assays in 835 convalescent sera. Secondly, we investigated the antibody response using the HAT after two doses of mRNA (BNT162b2) vaccination. Sera were collected at baseline, three weeks after the first and second vaccinations from older (80-99 years, Results: Here we show that HAT antibodies highly correlated with neutralising antibodies (R = 0.72-0.88) in convalescent sera. Home-dwelling older individuals have significantly lower antibodies to the Wuhan strain after one and two doses of BNT162b2 vaccine than younger adult vaccinees and naturally infected individuals. Moverover, a second vaccine dose boosts and broadens the antibody repertoire to VOC in naïve, not previously infected older and younger adults. Most (72-76%) older adults respond after two vaccinations to alpha and delta, but only 58-62% to beta and gamma, compared to 96-97% of younger vaccinees and 68-76% of infected individuals. Previously infected older individuals have, similarly to younger adults, high antibody titres after one vaccination. Conclusions: Overall, HAT provides a surrogate marker for neutralising antibodies, which can be used as a simple inexpensive, rapid test. HAT can be rapidly adaptable to emerging VOC for large-scale evaluation of potentially decreasing vaccine effectiveness.

Indexed as

Predictive markersRNA vaccinesViral infection

Identifiers

PMID35603265
PMCPMC9053181
OpenAlexW4226354556

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.