Evidence map›Paper›PMID 41601674›Full record

ArticleFrontiers in immunology2025

Postbiotic effects elicited by heat-inactivated

Franca Oglio, Lorella Paparo, Laura Carucci, Alessia Gaeta, Samantha Armiento, Serena Coppola, Antonio Molinaro, Cristina De Castro, Antonio Masino, Vittoria Mauriello and 5 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. 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.

Franca Oglio *Department of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Lorella Paparo *Department of Laboratory Medicine, Azienda Sanitaria Locale (ASL) Benevento, Benevento, Italy.
Laura CarucciDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Alessia GaetaInstitute of Genetics and Biophysics, Consiglio Nazionale delle Ricerche (CNR), Naples, Italy.
Samantha ArmientoDepartment of Chemical Sciences, University of Naples Federico II, Naples, Italy.
Serena CoppolaDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Antonio MolinaroDepartment of Chemical Sciences, University of Naples Federico II, Naples, Italy.
Cristina De CastroDepartment of Chemical Sciences, University of Naples Federico II, Naples, Italy.
Antonio MasinoDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Vittoria MaurielloDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Marco MicheliniDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Marica CozzolinoDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Rita NocerinoDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.
Laura PisapiaInstitute of Genetics and Biophysics, Consiglio Nazionale delle Ricerche (CNR), Naples, Italy.
Roberto Berni CananiDepartment of Translational Medical Science, University of Naples Federico II, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The probiotic Methods: Peripheral blood mononuclear cells (PBMCs) collected from IgE-mediated CMA children (n=6, all Caucasian, mean age 31.2 months) were stimulated with beta-lactoglobulin (BLG) in the absence or presence of LGGp. Activated regulatory T cells (Tregs)number was assessed by flowcytometry. Growth factors and cytokines modulating interleukins (IL) production were assessed by RT-PCR. IL-4, 5, 13 and 10 production was assessed by ELISA. The LGGp effects on gut barrier were evaluated using a Caco-2 cells-based experimental model by measuring transepithelial electrical resistance (TEER); tight junction proteins, Mucin-2 (Muc-2), and lactase expression; and FITC dextran permeability. Results: LGGp exposure resulted in Tregs activation and beneficial modulation of cytokines production in PBMCs from CMA patients. These effects paralleled with beneficial effects on all biomarkers of gut barrier integrity. Conclusions: Our data suggest that LGGp, modulating several immune tolerance mechanisms, could be a promising therapeutic strategy against CMA.

Indexed as

Lacticaseibacillus rhamnosusMilk HypersensitivityProbioticsAnimalsCaco-2 CellsCattleChild, PreschoolCytokinesFemaleHot TemperatureHumansImmune ToleranceImmunoglobulin EInfantIntestinal Barrier FunctionLactoglobulinsCytokinesImmunoglobulin ELactoglobulinscytokinesfood allergygut barrierimmune toleranceLGGTh2 response

Identifiers

PMID41601674
PMCPMC12832425

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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.