Evidence map›Paper›PMID 42174417›Full record

ArticleCellular & molecular biology letters2026

Neutrophils blend innate and adaptive immunity in early breast milk.

Gema Gomez-Casado, Natalia Saldaña-García, Antonio Cantarero-Cuenca, Andrés Gonzalez-Jimenez, Guillermo Paz-López, Patricia Garcia-Hurtado, Francisco J Tinahones, Ernesto González-Mesa, Almudena Ortega-Gomez

Abstract read
In one paragraph

Article in Cellular & molecular biology letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Gema Gomez-CasadoInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA Plataforma BIONAND), Universidad de Málaga, Málaga, Spain.
Natalia Saldaña-GarcíaInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA Plataforma BIONAND), Universidad de Málaga, Málaga, Spain.
Antonio Cantarero-CuencaBioinformatics Platform, Instituto de Investigación Biomédica de Málaga (IBIMA Plataforma BIONAND), Málaga, Spain.
Andrés Gonzalez-JimenezBioinformatics Platform, Instituto de Investigación Biomédica de Málaga (IBIMA Plataforma BIONAND), Málaga, Spain.
Guillermo Paz-LópezBioinformatics Platform, Instituto de Investigación Biomédica de Málaga (IBIMA Plataforma BIONAND), Málaga, Spain.
Patricia Garcia-HurtadoDepartment of Obstetrics and Gynecology, Regional University Hospital of Malaga, Málaga, Spain.
Francisco J TinahonesInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA Plataforma BIONAND), Universidad de Málaga, Málaga, Spain. fjtinahones@uma.es.
Ernesto González-Mesa *Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA Plataforma BIONAND), Universidad de Málaga, Málaga, Spain.
Almudena Ortega-Gomez *Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA Plataforma BIONAND), Universidad de Málaga, Málaga, Spain. almudena.ortega@ibima.eu.

Funding

Consejería de Salud y Consumo, Junta de Andalucía C1-0004-2025Consejería de Universidad, Investigación e Innovación de Andalucía. ProyExcel_00962Instituto de Salud Carlos III FI23/00104Instituto de Salud Carlos III PI22/01813
6 · The paper itself

Abstract

backgroundBreast milk not only is the most optimal source of nutrition for newborns but also provides crucial immune support. While there is extensive evidence highlighting the health benefits of breastfeeding, the scientific understanding behind many of these advantages remains limited. The immune cell fraction of breast milk has been poorly studied, and characterization of this essential component may be crucial to shed light on the subject. Here, we investigate the population of neutrophils in breast milk to unveil their phenotype and functions.

methodsNeutrophils in human breast milk were characterized by flow cytometry, and their phenotype was contrasted with that of their circulating counterparts using a paired approach. Transmission electron microscopy (TEM), intracellular granule immunocytochemistry, and Giemsa staining were employed to reveal their intracellular structure. In vitro neutrophil incubations were performed to assess the phenotypic modifications of circulating neutrophils in a breast milk environment. Functional assays were carried out to assess the activity of neutrophils and their potential impact on adaptive immunity. Finally, a proteomic approach was used on isolated neutrophils and their supernatant after cultivation to define the protein-based mechanisms involved in their biology. Paired t-tests and one- and two-way analysis of variance (ANOVA) were used for statistical analyses.

resultsIn the breast milk from the first 5 days (known as colostrum), neutrophils represent most of the cellular compartment. Colostrum neutrophils present a cell surface signature markedly different from circulating neutrophils with a clear CXCR4

conclusionsThis study provides evidence of a unique population of neutrophils in early breast milk connected to adaptive immunity, which may hold the key to understanding the mechanisms behind the immunological benefits of breastfeeding.

Indexed as

Adaptive ImmunityImmunity, InnateMilk, HumanNeutrophilsColostrumFemaleHumansAntigenBreast milkColostrumHumoral responseNeutrophilProteomics

Identifiers

PMID42174417
PMCPMC13308176

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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.