Evidence map›Paper›PMID 37328651›Full record

ArticleCommunications medicine2023

Hybrid immunity in older adults is associated with reduced SARS-CoV-2 infections following BNT162b2 COVID-19 immunisation.

Scott J C Pallett, Joseph Heskin, Fergus Keating, Andrea Mazzella, Hannah Taylor, Aatish Patel, Georgia Lamb, Deborah Sturdy, Natalie Eisler, Sarah Denny and 13 more

Abstract read
In one paragraph

Article in Communications medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
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  7. Post-Vaccination COVID-19 Infection among Health Care Workers: Description, Determinants, and Event-History Analysis.Indian journal of community medicine : official publication of Indian Association of Preventive & Social Medicine
    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

23 authors.

Scott J C Pallett *Clinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-9465-5299
Joseph Heskin *Clinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Fergus KeatingRoyal Hospital Chelsea, Royal Hospital Road, London, UK.
Andrea MazzellaInstitute for Infection and Immunity, St George's University of London, London, UK.ORCID http://orcid.org/0000-0003-1560-7465
Hannah TaylorArmy Health Branch, Army Headquarters, Andover, UK.
Aatish PatelClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-2503-2602
Georgia LambClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Deborah SturdyRoyal Hospital Chelsea, Royal Hospital Road, London, UK.
Natalie EislerRoyal Hospital Chelsea, Royal Hospital Road, London, UK.
Sarah DennyClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Esmita CharaniClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-5938-1202
Paul RandellNorth West London Pathology, London, UK.
Nabeela MughalClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Eleanor ParkerDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-9898-8568
Carolina Rosadas de OliveiraDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Michael RaymentClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Rachael JonesClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.
Richard TedderDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Myra McClureDepartment of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Elisabetta GroppelliInstitute for Infection and Immunity, St George's University of London, London, UK.
Gary W DaviesClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0001-9945-4616
Matthew K O'SheaCentre of Defence Pathology, Royal Centre for Defence Medicine, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
Luke S P MooreClinical Infection Department, Chelsea and Westminster NHS Foundation Trust, London, UK. luke.moore@nhs.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOlder adults, particularly in long-term care facilities (LTCF), remain at considerable risk from SARS-CoV-2. Data on the protective effect and mechanisms of hybrid immunity are skewed towards young adults precluding targeted vaccination strategies.

methodsA single-centre longitudinal seroprevalence vaccine response study was conducted with 280 LCTF participants (median 82 yrs, IQR 76-88 yrs; 95.4% male). Screening by SARS-CoV-2 polymerase chain reaction with weekly asymptomatic/symptomatic testing (March 2020-October 2021) and serology pre-/post-two-dose Pfizer-BioNTech BNT162b2 vaccination for (i) anti-nucleocapsid, (ii) quantified anti-receptor binding domain (RBD) antibodies at three time-intervals, (iii) pseudovirus neutralisation, and (iv) inhibition by anti-RBD competitive ELISA were conducted. Neutralisation activity: antibody titre relationship was assessed via beta linear-log regression and RBD antibody-binding inhibition: post-vaccine infection relationship by Wilcoxon rank sum test.

resultsHere we show neutralising antibody titres are 9.2-fold (95% CI 5.8-14.5) higher associated with hybrid immunity (p < 0.00001); +7.5-fold (95% CI 4.6-12.1) with asymptomatic infection; +20.3-fold, 95% (CI 9.7-42.5) with symptomatic infection. A strong association is observed between antibody titre: neutralising activity (p < 0.00001) and rising anti-RBD antibody titre: RBD antibody-binding inhibition (p < 0.001), although 18/169 (10.7%) participants with high anti-RBD titre (>100BAU/ml), show inhibition <75%. Higher RBD antibody-binding inhibition values are associated with hybrid immunity and reduced likelihood of infection (p = 0.003).

conclusionsHybrid immunity in older adults was associated with considerably higher antibody titres, neutralisation and inhibition capacity. Instances of high anti-RBD titre with lower inhibition suggests antibody quantity and quality as independent potential correlates of protection, highlighting added value of measuring inhibition over antibody titre alone to inform vaccine strategy.

Identifiers

PMID37328651
PMCPMC10275930

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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.