Evidence map›Paper›PMID 35891255›Full record

ArticleVaccines2022

Durability of Antibody Response after Primary Pneumococcal Double-Dose Prime-Boost Vaccination in Adult Kidney Transplant Recipients and Candidates: 18-Month Follow-Up in a Non-Blinded, Randomised Clinical Trial.

Lykke Larsen, Claus Bistrup, Søren Schwartz Sørensen, Lene Boesby, Charlotte Sværke Jørgensen, Christian Nielsen, Isik Somuncu Johansen

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 5 institutions in 1 country.

Lykke LarsenDepartment of Infectious Diseases, Odense University Hospital, 5000 Odense, Denmark.ORCID 0000-0002-4113-4182
Claus BistrupDepartment of Nephrology, Odense University Hospital, 5000 Odense, Denmark.ORCID 0000-0002-9280-916X
Søren Schwartz SørensenDepartment of Nephrology, Rigshospitalet, Copenhagen University Hospital, 2100 Copenhagen, Denmark.ORCID 0000-0001-5898-8048
Lene BoesbyDepartment of Medicine, Zealand University Hospital Roskilde, 4000 Roskilde, Denmark.ORCID 0000-0002-6326-3671
Charlotte Sværke JørgensenDepartment of Virus and Microbiological Special Diagnostics, Statens Serum Institut, 2300 Copenhagen, Denmark.ORCID 0000-0002-7156-1986
Christian NielsenDepartment of Clinical Immunology, Odense University Hospital, 5000 Odense, Denmark.ORCID 0000-0002-5711-6595
Isik Somuncu JohansenDepartment of Infectious Diseases, Odense University Hospital, 5000 Odense, Denmark.ORCID 0000-0002-2189-9823
University of Southern Denmark · DKOdense University Hospital · DKStatens Serum Institut · DKUniversity of Copenhagen · DKZealand University Hospital · DK

Funding

Aase & Ejnar Danielsen foundation 10-001896Augustinus Foundation 17-0185Foundation for "Lægevidenskabens Fremme" 16-212Grosserer L. F. Foghts foundation 21.262Helen & Ejnar Bjørnows foundation 04121Juchum foundation 34599Odense University Hospital A1399Region of Southern Denmark's PhD foundation SDUSF-2016-131University of Southern Denmark
6 · The paper itself

Abstract

backgroundPneumococcal prime-boost vaccination is recommended for solid organ transplant recipients and candidates. The long-term durability of the antibody (AB) response is unknown. The same applies to a dose-dependent immune response.

methodsWe studied the durability of the vaccine response after 18 months in kidney transplant recipients (KTRs) and patients on the kidney transplant waiting list (WLPs). Both groups received either a normal dose (ND) or a double dose (DD) of the 13-valent pneumococcal conjugate vaccine and the 23-valent pneumococcal polysaccharide vaccine. The average pneumococcal AB geometric mean concentration (GMC) was evaluated. A level ≥ 1 mg/L was considered protective against invasive pneumococcal disease (IPD).

resultsSixty WLPs and 70 KTRs were included. The proportion of participants protected declined from 52% to 33% in WLPs and from 29% to 16% in KTRs, with the previously significant dose-effect in WLPs no longer present (40% DD vs. 27% ND;

conclusionsAt follow-up, the pneumococcal prime-boost vaccination still provided significantly elevated average pneumococcal AB GMCs in both populations. Though the proportion of participants protected against IPD in WLP-DD and WLP-ND were statistically comparable, a DD may still be recommended for WLPs (EudraCT: 2016-004123-23).

Indexed as

13-valent pneumococcal conjugate vaccine23-valent pneumococcal polysaccharideimmunogenicitykidney transplant recipient

Identifiers

PMID35891255
PMCPMC9323946
OpenAlexW4284891827

What OpenQuestion holds

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LicenceCC BY
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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.