Evidence map›Paper›PMID 38090591›Full record

ArticleFrontiers in immunology2023

Humoral antibody response following mRNA vaccines against SARS-CoV-2 in solid organ transplant recipients; a status after a fifth and bivalent vaccine dose.

Emma Christophorou, Anna Christine Nilsson, Inge Petersen, Susan O Lindvig, Jesper R Davidsen, Rozeta Abazi, Mikael K Poulsen, Rune M Pedersen, Ulrik S Justesen, Nicolai E Johansen and 3 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-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

8 citing papers in PubMed, 7 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

13 authors at 2 institutions in 1 country.

Emma ChristophorouDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Anna Christine NilssonDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Inge PetersenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Susan O LindvigDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Jesper R DavidsenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Rozeta AbaziDepartment of Gastroenterology, Odense University Hospital, Odense, Denmark.
Mikael K PoulsenDepartment of Cardiology, Odense University Hospital, Odense, Denmark.
Rune M PedersenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Ulrik S JustesenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Nicolai E JohansenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Claus BistrupDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Lone W MadsenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Isik S JohansenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.
Odense University Hospital · DKUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In solid organ transplant (SOT) recipients, the humoral response following COVID-19 vaccination is reduced, as a result of their immunosuppressed treatment. In this study, we investigated antibody concentrations after booster vaccinations until the fifth dose, the latter by monovalent or bivalent BA1 or BA4/5 vaccines. In addition, we evaluated the efficacy of vaccination by recording breakthrough infections, hospitalizations, and deaths. Method: This prospective cohort study included 438 SOT recipients (>18 years) vaccinated with mRNA vaccines against COVID-19 from January 2021 until March 2023. Blood samples were drawn before and after each vaccination and tested for SARS-CoV-2 spike RBD IgG antibodies with the lowest and highest cut-off at 7.1 and 5,680 BAU/mL, respectively. Vaccine information, breakthrough infections, and hospitalizations were collected from the medical records. Results: Most participants received BNT162b2 and 61.4% received five vaccine doses. The response proportion in SOT recipients increased from 86.7% after the fourth dose to 93.0% following the fifth dose. Antibody concentration decreased with 142.7 BAU/mL between the third and fourth dose (median 132 days, Quartile 1: 123, Quartile 3: 148) and 234.3 BAU/mL between the fourth and fifth (median 250 days, Quartile 1: 241, Quartile 3: 262) dose among those without breakthrough infection (p=0.34). When comparing the Omicron BA.1 or Omicron BA.4/BA.5 adapted vaccines, no significant differences in antibody concentration were found, but 20.0% of SOT recipients receiving a monovalent fifth vaccine dose had a breakthrough infection compared to 4.0% and 7.9% among those who received BA.1 and BA.4/BA.5 adapted vaccines, respectively (p=0.04). Since January 2021, 240 (54.8%) participants had a breakthrough infection, and 22 were hospitalized, but no deaths were observed. Conclusions: The fifth COVID-19 vaccine dose raised antibody response to 93.0% of the study population. Additional booster doses, as well as bivalent vaccines, led to higher levels of antibody concentration in SOT recipients. We found a lower incidence of breakthrough infections among SOT recipients after receiving a bivalent vaccine as a fifth dose compared to those receiving a monovalent dose. Antibody concentrations did not wane when the time between doses was prolonged from four to eight months.

Indexed as

COVID-19COVID-19 VaccinesOrgan TransplantationAntibody FormationBNT162 VaccineBreakthrough InfectionsHumansImmunoglobulin GmRNA VaccinesProspective StudiesSARS-CoV-2Vaccines, CombinedBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GmRNA VaccinesVaccines, CombinedBA.1BA4/BA5bivalent vaccinesbreakthrough infectionsCOVID-19 vaccinationfifth dosehumoral responsesolid organ transplant

Identifiers

PMID38090591
PMCPMC10711048
OpenAlexW4389055732

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.