Evidence map›Paper›PMID 37234151›Full record

ArticleFrontiers in immunology2023

T cell immunity following COVID-19 vaccination in adult patients with primary antibody deficiency - a 22-month follow-up.

Antti Hurme, Pinja Jalkanen, Minna Marttila-Vaara, Jemna Heroum, Heidi Jokinen, Saimi Vara, Oona Liedes, Johanna Lempainen, Merit Melin, Ilkka Julkunen and 1 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  4. Review
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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

11 authors at 3 institutions in 1 country.

Antti HurmeDepartment of Infectious Diseases, Turku University Hospital and University of Turku, Turku, Finland.
Pinja JalkanenInstitute of Biomedicine, University of Turku, Turku, Finland.
Minna Marttila-VaaraDepartment of Infectious Diseases, Turku University Hospital and University of Turku, Turku, Finland.
Jemna HeroumInstitute of Biomedicine, University of Turku, Turku, Finland.
Heidi JokinenClinical Microbiology, Turku University Hospital, Turku, Finland.
Saimi VaraDepartment of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
Oona LiedesDepartment of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
Johanna LempainenInstitute of Biomedicine, University of Turku, Turku, Finland.
Merit MelinDepartment of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
Ilkka JulkunenInstitute of Biomedicine, University of Turku, Turku, Finland.
Leena KainulainenDepartment of Infectious Diseases, Turku University Hospital and University of Turku, Turku, Finland.
Turku University Hospital · FIUniversity of Turku · FIFinnish Institute for Health and Welfare · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary antibody deficiencies, such as common variable immunodeficiency (CVID), are heterogenous disease entities consisting of primary hypogammaglobulinemia and impaired antibody responses to vaccination and natural infection. CVID is the most common primary immunodeficiency in adults, presenting with recurrent bacterial infections, enteropathy, autoimmune disorders, interstitial lung diseases and increased risk of malignancies. Patients with CVID are recommended to be vaccinated against SARS-CoV-2, but there are relatively few studies investigating humoral and cellular responses to immunization. We studied the dynamics of humoral and cell-mediated immunity responses up to 22 months in 28 patients with primary immunodeficiency and three patients with secondary immunodeficiency receiving ChAdOx1, BNT162b2 and mRNA-1273 COVID-19 vaccines. Despite inadequate humoral response to immunization, we demonstrate a robust T cell activation likely protecting from severe COVID-19.

Indexed as

Common Variable ImmunodeficiencyCOVID-19Primary Immunodeficiency DiseasesAdultBNT162 VaccineCOVID-19 VaccinesFollow-Up StudiesHumansSARS-CoV-2T-LymphocytesVaccinationBNT162 VaccineCOVID-19 Vaccinescommon variable immunodeficiencyCOVID-19humoral immunityT cell mediated immunityvaccine

Identifiers

PMID37234151
PMCPMC10206403
OpenAlexW4378348350

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.