Evidence map›Paper›PMID 37095240›Full record

ArticleCommunications medicine2023

Impact of age and comorbidities on SARS-CoV-2 vaccine-induced T cell immunity.

Lisa Loksø Dietz, Anna Karina Juhl, Ole Schmeltz Søgaard, Joanne Reekie, Henrik Nielsen, Isik Somuncu Johansen, Thomas Benfield, Lothar Wiese, Nina Breinholt Stærke, Tomas Østergaard Jensen and 19 more

Open access · goldAbstract 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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
11.9field-weighted citation impact, top 1% 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

32 citing papers in PubMed, 61 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

29 authors at 11 institutions in 1 country.

Lisa Loksø Dietz *Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark. lisdie@rm.dk.ORCID http://orcid.org/0000-0002-1797-5766
Anna Karina Juhl *Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark. anajuh@rm.dk.ORCID http://orcid.org/0000-0001-6079-5173
Ole Schmeltz SøgaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-9107-2023
Joanne ReekieCenter of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-8529-3559
Henrik NielsenDepartment of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
Isik Somuncu JohansenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0002-2189-9823
Thomas BenfieldDepartment of Infectious Diseases, Copenhagen University Hospital-Amager and Hvidovre, Hvidovre, Denmark.ORCID http://orcid.org/0000-0003-0698-9385
Lothar WieseDepartment of Medicine, Zealand University Hospital, Roskilde, Denmark.
Nina Breinholt StærkeDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-5834-2033
Tomas Østergaard JensenCenter of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-0398-4431
Stine Finne JakobsenCenter of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-2586-0248
Rikke OlesenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Kasper IversenDepartment of Cardiology and Department of Emergency Medicine, Herlev Hospital, Herlev, Denmark.
Kamille FoghDepartment of Cardiology and Department of Emergency Medicine, Herlev Hospital, Herlev, Denmark.
Jacob BodilsenDepartment of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
Kristine Toft PetersenDepartment of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
Lykke LarsenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0002-4113-4182
Lone Wulff MadsenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Susan Olaf LindvigDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Inge Kristine HoldenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Dorthe RabenCenter of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Sidsel Dahl AndersenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Astrid Korning HvidtDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Signe Rode AndreasenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Eva Anna Marianne BaerendsDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Jens LundgrenCenter of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-8901-7850
Lars ØstergaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
ENFORCE Study Group
University of Copenhagen · DKAarhus University · DKUniversity of Southern Denmark · DKAalborg University Hospital · DKAarhus University Hospital · DKHerlev Hospital · DKStatens Serum Institut · DKZealand University Hospital · DKHvidovre Hospital · DKNational Board of Health · DKOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOlder age and chronic disease are important risk factors for developing severe COVID-19. At population level, vaccine-induced immunity substantially reduces the risk of severe COVID-19 disease and hospitalization. However, the relative impact of humoral and cellular immunity on protection from breakthrough infection and severe disease is not fully understood.

methodsIn a study cohort of 655 primarily older study participants (median of 63 years (IQR: 51-72)), we determined serum levels of Spike IgG antibodies using a Multiantigen Serological Assay and quantified the frequency of SARS-CoV-2 Spike-specific CD4 + and CD8 + T cells using activation induced marker assay. This enabled characterization of suboptimal vaccine-induced cellular immunity. The risk factors of being a cellular hypo responder were assessed using logistic regression. Further follow-up of study participants allowed for an evaluation of the impact of T cell immunity on breakthrough infections.

resultsWe show reduced serological immunity and frequency of CD4 + Spike-specific T cells in the oldest age group (≥75 years) and higher Charlson Comorbidity Index (CCI) categories. Male sex, age group ≥75 years, and CCI > 0 is associated with an increased likelihood of being a cellular hypo-responder while vaccine type is a significant risk factor. Assessing breakthrough infections, no protective effect of T cell immunity is identified.

conclusionsSARS-CoV-2 Spike-specific immune responses in both the cellular and serological compartment of the adaptive immune system increase with each vaccine dose and are progressively lower with older age and higher prevalence of comorbidities. The findings contribute to the understanding of the vaccine response in individuals with increased risk of severe COVID-19 disease and hospitalization.

Identifiers

PMID37095240
PMCPMC10124939
OpenAlexW4366816754

What OpenQuestion holds

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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.