Does Caesarean Section or Preterm Delivery Influence TGF-β2 Concentrations in Human Colostrum?


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
15 Apr 2020
Historique:
received: 03 03 2020
revised: 13 04 2020
accepted: 13 04 2020
entrez: 25 4 2020
pubmed: 25 4 2020
medline: 28 1 2021
Statut: epublish

Résumé

Human colostrum (HC) is a rich source of immune mediators that play a role in immune defences of a newly born infant. The mediators include transforming growth factor β (TGF-β) which exists in three isoforms that regulate cellular homeostasis and inflammation, can induce or suppress immune responses, limit T helper 1 cells (Th1) reactions and stimulate secretory immunoglobulin A (IgA) production. Human milk TGF-β also decreases apoptosis of intestinal cells and suppresses macrophage cytokine expression. The aim of the study was to determine the concentration of TGF-β2 in HC obtained from the mothers who delivered vaginally (VD) or by caesarean section (CS), and to compare the concentrations in HC from mothers who delivered at term (TB) or preterm (PB). In this study, 56% of preterm pregnancies were delivered via CS. The concentrations of TGF-β2 were measured in HC from 299 women who delivered in the 1st Department of Obstetrics and Gynaecology, Medical University of Warsaw: 192 (VD), 107 (CS), 251 (TB), and 48 (PB). The colostrum samples were collected within 5 days post-partum. TGF-β2 levels in HC were measured by the enzyme-linked immunosorbent assay (ELISA) test with the Quantikine ELISA Kit-Human TGF-β2 (cat.no. SB250). Statistical significance between groups was calculated by the Student

Identifiants

pubmed: 32326558
pii: nu12041095
doi: 10.3390/nu12041095
pmc: PMC7230194
pii:
doi:

Substances chimiques

Transforming Growth Factor beta2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Bożena Kociszewska-Najman (B)

Department of Neonatology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Elopy Sibanda (E)

Asthma, Allergy and Immune Dysfunction Clinic, Twin Palms Medical Centre, 113 Kwame Nkrumah Avenue, Harare, Zimbabwe.
Department of Pathology, Medical School, National University of Science and Technology, PO Box AC 939, Ascot, Bulawayo, Zimbabwe.
Division of Pathophysiology and Allergy Research, Medical University of Vienna, 1090 Vienna, Austria.

Dorota M Radomska-Leśniewska (DM)

Department of Histology and Embryology, Centre of Biostructure Research, Medical University of Warsaw, 02-004 Warsaw, Poland.

Karol Taradaj (K)

Students Scientific Research Group by Department of Neonatology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Patrycja Kociołek (P)

Students Scientific Research Group by Department of Neonatology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Tomasz Ginda (T)

Students Scientific Research Group by Department of Neonatology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Monika Gruszfeld (M)

Department of Neonatology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Ewa Jankowska-Steifer (E)

Department of Histology and Embryology, Centre of Biostructure Research, Medical University of Warsaw, 02-004 Warsaw, Poland.

Bronisława Pietrzak (B)

Department of Obstetrics and Gynaecology, Medical University of Warsaw, 02-015 Warsaw, Poland.

Mirosław Wielgoś (M)

Department of Obstetrics and Gynaecology, Medical University of Warsaw, 02-015 Warsaw, Poland.

Jacek Malejczyk (J)

Department of Histology and Embryology, Centre of Biostructure Research, Medical University of Warsaw, 02-004 Warsaw, Poland.

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