Evidence map›Paper›PMID 41087582›Full record

ArticleThe EMBO journal2025

Mechanisms of maternal antibody interference with rotavirus vaccination.

Tawny L Chandler, Sarah Woodyear, Valerie Chen, Tom M Lonergan, Natalie Baker, Katherine Harcourt, Simon Clare, Faraz Ahmed, Sarah L Caddy

Abstract read
In one paragraph

Article in The EMBO journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Probiotics as Potential Enhancers of Veterinary Vaccines.Probiotics and antimicrobial proteins · 2026
    Review
  4. Review
  5. Article
  6. 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

9 authors.

Tawny L Chandler *Baker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA.
Sarah Woodyear *Baker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA.ORCID http://orcid.org/0009-0006-5071-103X
Valerie ChenBaker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA.
Tom M LonerganBaker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA.
Natalie BakerBaker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA.ORCID http://orcid.org/0009-0001-0586-2828
Katherine HarcourtDepartment of Medicine, University of Cambridge, Cambridge, CB2 0QH, UK.
Simon ClareDepartment of Medicine, University of Cambridge, Cambridge, CB2 0QH, UK.
Faraz AhmedGenomics Innovation Hub and TREx Facility, Institute of Biotechnology, Cornell University, Ithaca, NY, 14850, USA.ORCID http://orcid.org/0000-0003-4774-8262
Sarah L CaddyBaker Institute for Animal Health, Cornell University, Ithaca, NY, 14850, USA. sarahcaddy@cornell.edu.ORCID http://orcid.org/0000-0002-9790-7420

Funding

Wellcome TrustWellcome Trust (WT) 211138/A/18/Z
6 · The paper itself

Abstract

Maternal antibodies are transferred transplacentally to fetuses and then through lactation to infants to protect them whilst their own immune system is still immature. However, these maternal antibodies also suppress neonatal B-cell responses, thereby impairing vaccine efficacy and leaving infants potentially vulnerable to life-threatening pathogens, such as rotaviruses. Currently available rotavirus vaccines are composed of live-attenuated viral strains administered to infants orally at 6-8 weeks old. Although high concentrations of maternal antibodies correlate with poor production of antibodies following vaccination (i.e., seroconversion), the immunological basis of this interference is unknown. To investigate the underlying mechanisms, we here developed a mouse model of neonatal oral rotavirus vaccination, in which vaccination only fails to induce seroconversion if maternal antibodies are present. Such antibodies are shown to block vaccine replication, while faster maternal antibody waning is observed in vaccinated compared to unvaccinated pups. FcγRIIB deletion does not overcome interference in pups, although pup IgG levels increase when maternal antibody titers are very low. Our findings show that maternal antibody-mediated vaccine clearance is a key mechanism of interference with oral rotavirus vaccines, with a minor role for FcγRIIB in neonatal IgG responses.

Indexed as

Antibodies, ViralImmunity, Maternally-AcquiredRotavirusRotavirus InfectionsRotavirus VaccinesAnimalsAnimals, NewbornFemaleImmunoglobulin GMiceMice, Inbred C57BLMice, KnockoutReceptors, IgGVaccinationAntibodies, ViralImmunoglobulin GReceptors, IgGRotavirus VaccinesFcγRIIBMaternal AntibodyRotavirusVaccine

Identifiers

PMID41087582
PMCPMC12623505

What OpenQuestion holds

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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.