Evidence map›Paper›PMID 35720400›Full record

ArticleFrontiers in immunology2022

Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study.

Adrian M Shields, Sian E Faustini, Harriet J Hill, Saly Al-Taei, Chloe Tanner, Fiona Ashford, Sarita Workman, Fernando Moreira, Nisha Verma, Hollie Wagg and 18 more

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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

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  15. Detection of specific RBDFrontiers in immunology · 2023
    Article
  16. Article
  17. Cohort profile:BMJ open · 2022
    Article
  18. Functional immunity against SARS-CoV-2 in the general population after a booster campaign and the Delta and Omicron waves, Switzerland, March 2022.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2022
    Article
  19. Article
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

28 authors at 12 institutions in 1 country.

Adrian M ShieldsClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Sian E FaustiniClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Harriet J HillInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Saly Al-TaeiClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Chloe TannerClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Fiona AshfordClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Sarita WorkmanDepartment of Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Fernando MoreiraDepartment of Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Nisha VermaDepartment of Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Hollie WaggInstitute of Translational Medicine, University of Birmingham, Birmingham, United Kingdom.
Gail HeritageInstitute of Translational Medicine, University of Birmingham, Birmingham, United Kingdom.
Naomi CamptonInstitute of Translational Medicine, University of Birmingham, Birmingham, United Kingdom.
Zania StamatakiInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Mark T DraysonClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Paul KlenermanNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
James E D ThaventhiranMedical Research Council Toxicology Unit, University of Cambridge, Cambridge, United Kingdom.
Shuayb ElkhalifaDepartment of Immunology, Salford Royal NHS Foundation Trust, Salford, United Kingdom.
Sarah GoddardDepartment of Clinical Immunology, University Hospitals North Midlands, Stoke-on-Trent, United Kingdom.
Sarah JohnstonDepartment of Clinical Immunology, North Bristol NHS Trust, Bristol, United Kingdom.
Aarnoud HuissoonDepartment of Clinical Immunology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.
Claire BethuneDepartment of Allergy and Clinical Immunology, University Hospitals Plymouth NHS Trust, Plymouth, United Kingdom.
Suzanne ElcombeDepartment of Allergy and Clinical Immunology, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, United Kingdom.
David M LoweDepartment of Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Smita Y PatelNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Sinisa SavicDepartment of Allergy and Clinical Immunology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Alex G RichterClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Siobhan O BurnsDepartment of Immunology, Royal Free London NHS Foundation Trust, London, United Kingdom.
COV-AD consortium
University of Birmingham · GBRoyal Free London NHS Foundation Trust · GBUniversity College London · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Oxford · GBLeeds Teaching Hospitals NHS Trust · GBMedical Research Council · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBNorth Bristol NHS Trust · GBSalford Royal NHS Foundation Trust · GBUniversity Hospitals of North Midlands NHS Trust · GBUniversity Hospitals Plymouth NHS Trust · GB

Funding

Medical Research Council MR/W002663/1MRF_ MRF-169-0001-F-STAM-C0826
6 · The paper itself

Abstract

Background: Patients with primary and secondary antibody deficiency are vulnerable to COVID-19 and demonstrate diminished responses following two-dose SARS-CoV-2 vaccine schedules. Third primary vaccinations have been deployed to enhance their humoral and cellular immunity. Objectives: To determine the immunogenicity of the third primary SARS-CoV-2 immunisation in a heterogeneous cohort of patients with antibody deficiency. Methods: Participants enrolled in the COV-AD study were sampled before and after their third vaccine dose. Serological and cellular responses were determined using ELISA, live-virus neutralisation and ELISPOT assays. Results: Following a two-dose schedule, 100% of healthy controls mounted a serological response to SARS-CoV-2 vaccination, however, 38.6% of individuals with antibody deficiency remained seronegative. A third primary SARS-CoV-2 vaccine significantly increased anti-spike glycoprotein antibody seroprevalence from 61.4% to 76.0%, the magnitude of the antibody response, its neutralising capacity and induced seroconversion in individuals who were seronegative after two vaccine doses. Vaccine-induced serological responses were broadly cross-reactive against the SARS-CoV-2 B.1.1.529 variant of concern, however, seroprevalence and antibody levels remained significantly lower than healthy controls. No differences in serological responses were observed between individuals who received AstraZeneca ChAdOx1 nCoV-19 and Pfizer BioNTech 162b2 during their initial two-dose vaccine schedule. SARS-CoV-2 infection-naive participants who had received a heterologous vaccine as a third dose were significantly more likely to have a detectable T cell response following their third vaccine dose (61.5% vs 11.1%). Conclusion: These data support the widespread use of third primary immunisations to enhance humoral immunity against SARS-CoV-2 in individuals with antibody deficiency.

Indexed as

COVID-19Viral VaccinesAntibodies, ViralAntibody FormationChAdOx1 nCoV-19COVID-19 VaccinesHumansSARS-CoV-2Seroepidemiologic StudiesVaccinationAntibodies, ViralChAdOx1 nCoV-19COVID-19 VaccinesViral VaccinesCOVID-19CVIDinborn errors of immunityprimary immunodeficiencySARS-CoV-2secondary immunodeficiencyvaccination

Identifiers

PMID35720400
PMCPMC9201027
OpenAlexW4285742145

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.