Evidence map›Paper›PMID 37592804›Full record

ArticleThe Journal of infectious diseases2024

Vaccine Take of RV3-BB Rotavirus Vaccine Observed in Indonesian Infants Regardless of HBGA Status.

Celeste M Donato, Amanda Handley, Sean G Byars, Nada Bogdanovic-Sakran, Eleanor A Lyons, Emma Watts, Darren S Ong, Daniel Pavlic, Jarir At Thobari, Cahya Dewi Satria and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 6 institutions in 3 countries.

Celeste M DonatoEnteric Diseases Group, Murdoch Children's Research Institute.ORCID 0000-0001-9262-6550
Amanda HandleyEnteric Diseases Group, Murdoch Children's Research Institute.
Sean G ByarsFlorey Institute of Neuroscience and Mental Health, Parkville, Australia.
Nada Bogdanovic-SakranEnteric Diseases Group, Murdoch Children's Research Institute.
Eleanor A LyonsEnteric Diseases Group, Murdoch Children's Research Institute.
Emma WattsEnteric Diseases Group, Murdoch Children's Research Institute.
Darren S OngEnteric Diseases Group, Murdoch Children's Research Institute.
Daniel PavlicEnteric Diseases Group, Murdoch Children's Research Institute.
Jarir At ThobariDepartment of Pharmacology and Therapy.
Cahya Dewi SatriaDepartment of Paediatrics.
Hera NirwatiCenter for Child Health.
Yati SoenartoCenter for Child Health.
Julie E BinesEnteric Diseases Group, Murdoch Children's Research Institute.
Murdoch Children's Research Institute · AUUniversitas Gadjah Mada · IDCenter for Global Development · USFlorey Institute of Neuroscience and Mental Health · AURoyal Children's Hospital · AUThe University of Melbourne · AU

Funding

Gates Foundation OPP1127967
6 · The paper itself

Abstract

backgroundHisto-blood group antigen (HBGA) status may affect vaccine efficacy due to rotavirus strains binding to HBGAs in a P genotype-dependent manner. This study aimed to determine if HBGA status affected vaccine take of the G3P[6] neonatal vaccine RV3-BB.

methodsDNA was extracted from stool samples collected in a subset (n = 164) of the RV3-BB phase IIb trial in Indonesian infants. FUT2 and FUT3 genes were amplified and sequenced, with any single-nucleotide polymorphisms analyzed to infer Lewis and secretor status. Measures of positive cumulative vaccine take were defined as serum immune response (immunoglobulin A or serum-neutralizing antibody) and/or stool excretion of RV3-BB virus. Participants were stratified by HBGA status and measures of vaccine take.

resultsIn 147 of 164 participants, Lewis and secretor phenotype were determined. Positive vaccine take was recorded for 144 (97.9%) of 147 participants with the combined phenotype determined. Cumulative vaccine take was not significantly associated with secretor status (relative risk, 1.00 [95% CI, .94-1.06]; P = .97) or Lewis phenotype (relative risk, 1.03 [95% CI, .94-1.14]; P = .33), nor was a difference observed when analyzed by each component of vaccine take.

conclusionsThe RV3-BB vaccine produced positive cumulative vaccine take, irrespective of HBGA status in Indonesian infants.

Indexed as

Blood Group AntigensRotavirusRotavirus InfectionsRotavirus VaccinesGenotypeHumansIndonesiaInfantInfant, NewbornBlood Group AntigensRotavirus Vaccineshisto-blood group antigenIndonesianeonatal vaccinationrotavirusvaccine take

Identifiers

PMID37592804
PMCPMC11011179
OpenAlexW4385969681

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LicenceCC BY
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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.