Evidence map›Paper›PMID 39176090›Full record

ArticleFrontiers in immunology2024

Extracellular vesicles derived from antigen-presenting cells pulsed with foot and mouth virus vaccine-antigens act as carriers of viral proteins and stimulate B cell response.

Florencia Menay, Federico Cocozza, Maria J Gravisaco, Analia Elisei, Javier Ignacio Re, Alejandra Ferella, Claudia Waldner, Claudia Mongini

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
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  5. Article
  6. Frontiers in microbiology · 2026
    Article
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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

8 authors.

Florencia MenayLaboratorio de Microvesículas, Exosomas y miRNA, Instituto de Virología y Innovaciones Tecnológicas (IVIT)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.
Federico CocozzaInstitut National de la Santé et de la Recherche Médicale (INSERM-U932), Institut Curie, París, France.
Maria J GravisacoCentro de Investigación en Ciencias Veterinarias y Agronómicas (CICVYA), Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.
Analia EliseiCentro de Investigación en Ciencias Veterinarias y Agronómicas (CICVYA), Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.
Javier Ignacio ReCentro de Investigación en Ciencias Veterinarias y Agronómicas (CICVYA), Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.
Alejandra FerellaLaboratorio de Microvesículas, Exosomas y miRNA, Instituto de Virología y Innovaciones Tecnológicas (IVIT)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.
Claudia WaldnerLaboratorio de Inmunología Celular y Molecular, Centro de Estudios Farmacologicos y Botanicos (CEFYBO) CONICET, Ciudad Autónoma de Buenos Aires, Argentina.
Claudia MonginiLaboratorio de Microvesículas, Exosomas y miRNA, Instituto de Virología y Innovaciones Tecnológicas (IVIT)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot and mouth disease (FMD) is a highly contagious infection caused by FMD-virus (FMDV) that affects livestock worldwide with significant economic impact. The main strategy for the control is vaccination with FMDV chemically inactivated with binary ethylenimine (FMDVi). In FMDV infection and vaccination, B cell response plays a major role by providing neutralizing/protective antibodies in animal models and natural hosts. Extracellular vesicles (EVs) and small EVs (sEVs) such as exosomes are important in cellular communication. EVs secreted by antigen-presenting cells (APC) like dendritic cells (DCs) participate in the activation of B and T cells through the presentation of native antigen membrane-associated to B cells or by transferring MHC-peptide complexes to T cells and even complete antigens from DCs. In this study, we demonstrate for the first time that APC activated with the FMDVi O1 Campos vaccine-antigens secrete EVs expressing viral proteins/peptides that could stimulate FMDV-specific immune response. The secretion of EVs-FMDVi is a time-dependent process and can only be isolated within the first 24 h post-activation. These vesicles express classical EVs markers (CD9, CD81, and CD63), along with immunoregulatory molecules (MHC-II and CD86). With an average size of 155 nm, they belong to the category of EVs. Studies conducted

Indexed as

Antigen-Presenting CellsAntigens, ViralB-LymphocytesExtracellular VesiclesFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusViral VaccinesAnimalsAntigen PresentationDendritic CellsLymphocyte ActivationViral ProteinsAntigens, ViralViral ProteinsViral Vaccinesantigen presenting cellsantiviral immune responseB cell activationextracellular vesiclesfoot and mouth disease virus

Identifiers

PMID39176090
PMCPMC11338771

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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.