Evidence map›Paper›PMID 37033955›Full record

ArticleFrontiers in immunology2023

Cellular and humoral immunogenicity of the COVID-19 vaccine and COVID-19 disease severity in individuals with immunodeficiency.

C E Murray, C O'Brien, S Alamin, S H Phelan, R Argue, R Kiersey, M Gardiner, A Naughton, E Keogh, P Holmes 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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 2 institutions in 1 country.

C E MurrayDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
C O'BrienDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
S AlaminDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
S H PhelanDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
R ArgueDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
R KierseyDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
M GardinerDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
A NaughtonDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
E KeoghDepartment of Biochemistry, St. James's Hospital, Dublin, Ireland.
P HolmesDepartment of Biochemistry, St. James's Hospital, Dublin, Ireland.
S NaughtonDepartment of Biochemistry, St. James's Hospital, Dublin, Ireland.
A ScanlonDepartment of Biochemistry, St. James's Hospital, Dublin, Ireland.
A SloanDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
P McCreaDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
J SuiDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
J DunneDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
N ConlonDepartment of Immunology, St. James's Hospital, Dublin, Ireland.
St. James's Hospital · IETrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A well-coordinated adaptive immune response is crucial for limiting COVID-19 disease. Some individuals with immunodeficiency are at a high risk of developing severe COVID-19. Therefore, the development of standardized methods for measuring different arms of the vaccine response in the setting of immunodeficiency is of particular interest. In this study, we compared the vaccine response of individuals living with immunodeficiency with healthy controls in terms of interferon gamma (IFN-γ) production and spike protein-specific antibody level post primary COVID-19 vaccination and booster vaccines. Additionally, the disease severity of those individuals who contracted COVID-19 was assessed. Methods: Whole blood was stimulated overnight from 71 participants and 99 healthy controls. Commercially available PepTivator Results: 99% of healthy controls, 89% of individuals with IEI and 76% with secondary immunodeficiency (SID) had an IFN-γ level above the validated reference range after peptide mix stimulation following primary vaccination. There was an increase in IFN-γ levels in patients with inborn errors of immunity (IEI) following the booster vaccine (p = 0.0156). 100% of healthy controls, 70% of individuals living with IEI and 64% of individuals living with SID had detectable spike protein-specific antibody levels following the primary vaccination. 55% of immunodeficiency patients who had mild COVID-19 and 10% with moderate/severe COVID-19 had detectable antibody and IFN-γ levels post vaccine. The mean pre-infection IDDA 2.1 scores were higher in individuals who developed moderate/severe COVID-19 (25.2 compared to 9.41). Conclusions: Covid whole-blood IGRA is a highly accurate, straightforward and robust assay and can be easily adapted to measure cellular response to COVID-19. A complete evaluation of the vaccine response may be particularly important for individuals living with immunodeficiency. A clinical immunodeficiency score and a validated vaccine response score may be valuable tools in estimating COVID-19 disease risk and identifying individuals living with immunodeficiency who may benefit from enhanced vaccination schedules.

Indexed as

COVID-19Immunologic Deficiency SyndromesCOVID-19 VaccinesHumansInterferon-gammaPatient AcuitySARS-CoV-2Spike Glycoprotein, CoronavirusCOVID-19 VaccinesInterferon-gammaSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2clinical scoring systemsCOVID-19 vaccinationIGRA methodsimmunodeficiencies affecting cellular and humoral immunityspike protein specific ELISA

Identifiers

PMID37033955
PMCPMC10080028
OpenAlexW4360868553

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.