Evidence map›Paper›PMID 41668982›Full record

ArticleFrontiers in allergy2025

A new experimental model of peanut allergy in BALB/c and C57BL/6 mice.

Marcos Felipe Andrade-Oliveira, Rafael Saavedra Langer, Sara Cândida Barbosa, Mariana Almeida Oliveira, Cecília Horta Ramalho-Pinto, Giovanna Caliman Camatta, Jamil Silvano de Oliveira, Igor de Campos Fontes, Fabiana Simão Machado, Carlos Delfin Chávez-Olórtegui and 3 more

Abstract read
In one paragraph

Article in Frontiers in allergy, 2025. 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
–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

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

13 authors.

Marcos Felipe Andrade-OliveiraDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Rafael Saavedra LangerDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Sara Cândida BarbosaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Mariana Almeida OliveiraDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Cecília Horta Ramalho-PintoDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Giovanna Caliman CamattaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Jamil Silvano de OliveiraDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Igor de Campos FontesDepartamento de Patologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Fabiana Simão MachadoDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Carlos Delfin Chávez-OlórteguiDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Tatiani Uceli MaioliDepartamento de Nutrição, Escola de Enfermagem, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Denise Carmona CaraDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Ana Maria Caetano FariaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Food allergy protocols are highly variable. While it allows the exploration of multiple scientific questions, it limits the possibility to make general assumptions and point out specific features of allergy to different food allergens. Considering this, our research group has developed a standardized food allergy protocol that has allowed us to study egg, milk and shrimp allergy. Methodology: In this study, we used the same protocol to develop a model of peanut allergy. BALB/c and C57BL/6 mice were sensitized with a subcutaneous injection of 40mg of peanut protein extract (PPE) adsorbed in 3mg of aluminum hydroxide (Al(OH) Results: After oral challenge, BALB/c and C57BL/6 sensitized mice had higher levels of total and specific IgE in the serum, as well as specific IgG1, than control groups. BALB/c, but not C57BL/6, mice presented higher levels of anti-PPE secretory IgA (SIgA), and lower reactivity to fecal bacteria than control group. Sensitized mice from both strains presented positive cutaneous anaphylaxis reaction. Systemic anaphylaxis was more prominent in C57BL/6 mice, while increase in gastrointestinal transit time was more prominent in BALB/c mice. Lastly, jejunum of BALB/c and C57BL/6 sensitized mice presented higher eosinophil, intraepithelial lymphocyte, and goblet cell count, as well as smaller villi length, than control groups. Conclusion: Our standardized food allergy protocol enabled the development of a peanut allergy model in two different mouse strains, which not only allows the study of peanut allergy itself, but also its comparison to other allergies triggered by food proteins.

Indexed as

anaphylaxisfood allergygut inflammationIgEpeanutsecretory IgA

Identifiers

PMID41668982
PMCPMC12883646

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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.