Evidence map›Paper›PMID 40266125›Full record

ArticleVaccines2025

Impact of Extended Dosing Intervals and Ipsilateral Versus Contralateral Boosting on mRNA Vaccine Immunogenicity in Mice.

Bin Lu, Omkar Chaudhary, Balaji Banoth, Janhavi Nadkarni, Wei Zong, Emilie Mausser, Hillary Danz, Mona Motwani, Sophie Ruiz, Donghui Zhang and 5 more

Abstract read
In one paragraph

Article in Vaccines, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Bin LumRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Omkar ChaudharymRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Balaji BanothFormer Employee of Sanofi, 200 West St., Waltham, MA 02451, USA.
Janhavi NadkarnimRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Wei ZongTranslational and Early Development Biostatistics, Sanofi, 200 West St., Waltham, MA 02451, USA.
Emilie MaussermRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.ORCID 0000-0001-5920-8808
Hillary DanzmRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Mona MotwanimRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Sophie RuizmRNA Center of Excellence, Sanofi, 1541 Avenue Marcel Mérieux, 69280 MarcyL'Etoile, France.ORCID 0000-0002-1919-3100
Donghui ZhangTranslational and Early Development Biostatistics, Sanofi, 200 West St., Waltham, MA 02451, USA.
Gopinath NageshwaranGlobal Antigen Design, Sanofi, 200 West St., Waltham, MA 02451, USA.ORCID 0000-0002-2682-381X
Bachra RokbiGlobal Antigen Design, Sanofi, 1541 Avenue Marcel Mérieux, 69280 Marcy L'Etoile, France.
William WarrenGlobal Antigen Design, Sanofi, 200 West St., Waltham, MA 02451, USA.
Frank DeRosamRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.
Sudha ChivukulamRNA Center of Excellence, Sanofi, 200 West St., Waltham, MA 02451, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough mRNA vaccines have the potential to be developed and deployed rapidly to combat infectious diseases, the ideal method of administration and boosting schedule strategy for generating optimal immunogenicity is an area of active research. We compared the immune responses resulting from different schedules for prime-boost and boosting either ipsilaterally or contralaterally in relation to the initial vaccine dose.

methodsInfluenza hemagglutinin (HA) was used as a model antigen for different vaccination regimens in mice using both mRNA lipid nanoparticles (mRNA-LNP) and AF03-adjuvanted recombinant protein (rHA-AF03) vaccines.

resultsIncreasing the prime-boost interval resulted in higher levels of serum anti-HA IgG and functional antibody hemagglutination inhibition (HAI) responses in mRNA-LNP-vaccinated animals, which correlated with an induction of germinal center (GC) B cells and follicular helper T (Tfh) cells in lymph nodes. In addition, longer prime-boost intervals resulted in higher levels of IL-2 and TNF-α producing CD4+ T cells two weeks after boosting. The number of Ig-secreting long-lived plasma cells increased with the length of prime-boost intervals. Contralateral boosting resulted in an increase in HAI titers and GC B cells compared to an ipsilateral boost. However, significantly higher numbers of GC B cells were induced in the draining lymph nodes following ipsilateral boosting than in the non-draining lymph nodes.

conclusionsOverall, our data provides insights into the immune mechanisms of action of mRNA-LNP to develop the optimal vaccine regimen for mRNA vaccine platforms.

Indexed as

contralateralimmunogenicityinfluenzaipsilateralmRNA-LNPprime–boost intervalvaccines

Identifiers

PMID40266125
PMCPMC11946721

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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.