Evidence map›Paper›PMID 42378964›Full record

ArticleEBioMedicine2026

Early-life gut microbiome composition and rotavirus vaccine-induced IgA responses in U.S. infants: a longitudinal cohort study.

Janiret Narváez-Miranda, Michael B Sohn, Daniel Velasquez-Portocarrero, Ann L Gill, Robert Beblavy, Darline Castro-Melendez, Kelechi Ejiofor, Xing Qiu, Nathan Laniewski, Brandon Groff and 9 more

Abstract read
In one paragraph

Article in EBioMedicine, 2026. 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
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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.

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

19 authors.

Janiret Narváez-MirandaDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Michael B SohnDepartments of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Daniel Velasquez-PortocarreroCenters for Disease Control and Prevention, Atlanta, GA, USA.
Ann L GillDepartment of Immunology, Microbiology and Virology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Robert BeblavyDepartments of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Darline Castro-MelendezDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Kelechi EjioforDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Xing QiuDepartments of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Nathan LaniewskiDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Brandon GroffClinical and Translational Sciences Institute, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Jessica BrunnerDepartment of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Meghan RasDepartment of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Alena LegerDepartment of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Allison MacomberDepartment of Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Sarah L CaddyBaker Institute for Animal Health, Cornell University, Ithaca, NY, USA.
Baoming JiangCenters for Disease Control and Prevention, Atlanta, GA, USA.
Tom O'ConnorDepartments of Psychiatry, Neuroscience, Obstetrics and Gynecology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Steven R GillDepartment of Immunology, Microbiology and Virology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Kristin ScheibleDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA. Electronic address: Kristin_Scheible@urmc.rochester.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRotavirus remains a leading cause of childhood mortality worldwide, despite the widespread introduction of oral rotavirus vaccines. Evidence linking the gut microbiome to vaccine response is inconsistent and limited in U.S. POPULATIONS: This study investigates the development of the infant gut microbiome and its association with immunogenicity following RotaTeq administration in U.S. infants.

methodsWe conducted a longitudinal analysis of infants in Rochester, New York, using 16S rRNA sequencing to assess microbiome composition at one (M1), sixth (M6), and twelfth (M12) months of age. Rotavirus-IgA serologies were measured at M6 and M12 to assess RotaTeq vaccine seroresponse. Clinical metadata were used to assess factors associated with microbial diversity and rotavirus-IgA titres over the first year of life. We examined associations between (1) M1 microbiome and M6 rotavirus-IgA; (2) M6 microbiome and M6 rotavirus-IgA; and (3) M6 microbiome and M12 rotavirus-IgA.

findingsHigher gut microbial alpha diversity at M1 was associated with higher rotavirus-IgA titres at M6 (N = 47, β: 2·06, 95% CI: [0·31-3·99], p = 0·024). Alpha diversity at M6 was not associated with concurrent rotavirus-IgA responses (N = 56, β: 0·73, 95% CI: [-0·856, 2·313], p = 0·36) but was associated with higher rotavirus-IgA at M12 (N = 52, β: 1·47, 95% CI: [0·127, 2·805], p = 0·033). Rotavirus-IgA responses were associated with specific microbial taxa across timepoints, with both positive and negative associations observed.

interpretationIn a healthy U.S. infant cohort, early-life gut microbiome diversity and composition were associated with rotavirus-IgA responses following RotaTeq vaccination. This study advances understanding of microbiome-vaccine interactions in high-income settings.

fundingOffice of the Director of the National Institutes of Health, National Institute of Mental Health of the National Institutes of Health, and the National Center for Advancing Translational Sciences of the National Institutes of Health.

Indexed as

Antibodies, ViralGastrointestinal MicrobiomeImmunoglobulin ARotavirusRotavirus InfectionsRotavirus VaccinesFemaleHumansInfantLongitudinal StudiesMaleRNA, Ribosomal, 16SUnited StatesVaccines, AttenuatedAntibodies, ViralImmunoglobulin ARNA, Ribosomal, 16SRotaTeqRotavirus VaccinesVaccines, AttenuatedEarly-life microbiomeImmunoglobulin AInfant microbiomeMicrobiotaRotavirus immunogenicityRotavirus vaccines

Identifiers

PMID42378964
PMCPMC13333288

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LicenceCC BY-NC-ND
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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.