Evidence map›Paper›PMID 39203970›Full record

ArticleVaccines2024

Comparison of Post-Vaccination Response (Humoral and Cellular) to BNT162b2 in Clinical Cases, Kidney and Pancreas Transplant Recipient with Immunocompetent Subjects over Almost Two Years of Parallel Monitoring.

Jaroslaw Walory, Iza Ksiazek, Karolina Wegrzynska, Anna Baraniak

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

4 authors.

Jaroslaw WaloryDepartment of Pharmaceutical Microbiology and Laboratory Diagnostics, National Medicines Institute, 00-725 Warsaw, Poland.ORCID 0000-0003-2352-2621
Iza KsiazekDepartment of Biochemistry and Biopharmaceuticals, National Medicines Institute, 00-725 Warsaw, Poland.ORCID 0000-0002-4315-6991
Karolina WegrzynskaDepartment of Pharmaceutical Microbiology and Laboratory Diagnostics, National Medicines Institute, 00-725 Warsaw, Poland.ORCID 0000-0003-4030-6795
Anna BaraniakDepartment of Pharmaceutical Microbiology and Laboratory Diagnostics, National Medicines Institute, 00-725 Warsaw, Poland.ORCID 0000-0001-9996-8553

Funding

National Medicines Institute DS12/2024
6 · The paper itself

Abstract

backgroundVaccination is one of the most effective medical interventions to prevent infectious diseases. The introduction of vaccines against coronavirus acute respiratory syndrome 2 (SARS-CoV-2) was aimed at preventing severe illness and death due to coronavirus disease 2019 (COVID-19). Solid organ transplant recipients (SOTRs) are at high risk of infection with SARS-CoV-2 and serious effects associated with COVID-19, mainly due to the use of immunosuppressive therapies, which further cause suboptimal response to COVID-19 vaccination. AIM OF THE STUDY: We aimed to compare post-vaccination response to BNT162b2 in kidney-pancreas transplant recipient, specifically in immunocompetent individuals, over two years of simultaneous monitoring.

methodsTo determine the humoral response, the levels of the IgG and IgA anti-S1 antibodies were measured. To assess the cellular response to SARS-CoV-2, the released IFN-γ-S1 was determinate. RESULTS AND

conclusionAfter primary vaccination, compared to immunocompetent subjects, SOTR showed lower seroconversion for both antibody classes. Only the additional dose produced antibodies at the level reached by the control group after the baseline vaccination. During the monitored period, SOTR did not achieve a positive cellular response in contrast to immunocompetent individuals, so in order to obtain longer protection, including immune memory, the adoption of booster doses of the vaccine should be considered.

Indexed as

anti-SARS-CoV-2 antibodiescellular responsehumoral responseIFN γimmunocompromised patientimmunosuppressionmRNA vaccine

Identifiers

PMID39203970
PMCPMC11360542

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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.