IL10 and CXCL10 mRNA expression in food protein-induced enterocolitis syndrome.

CXCL10 Children Food protein–induced enterocolitis syndrome (FPIES) IL10

Journal

Cytokine
ISSN: 1096-0023
Titre abrégé: Cytokine
Pays: England
ID NLM: 9005353

Informations de publication

Date de publication:
11 Aug 2024
Historique:
received: 07 06 2024
revised: 23 07 2024
accepted: 24 07 2024
medline: 13 8 2024
pubmed: 13 8 2024
entrez: 12 8 2024
Statut: aheadofprint

Résumé

Food protein-induced enterocolitis syndrome (FPIES) is a rare non-IgE-mediated food allergy that mainly impacts babies and 7toddlers. The exact mechanism of FPIES is not completely understood. By studying the expression of IL-10 and CXCL10 in pediatric FPIES patients, researchers can gain insights into the immune mechanisms underlying this disorder. Peripheral venous blood was collected and subsequently stabilized with RNA pro. Total RNA was extracted and mRNA levels of CXCL10 and IL-10 was determined with real time PCR. Children with FPIES had significantly higher values than the healthy control group (HC) for CXCL10 while FPIES had a significant lower values than the control group for IL-10. Our results show a high production of CXCL10 and a concomitant reduced production of IL-10 in FPIES subjects who have not yet reached tolerance. These data may represent a molecular diagnostic marker for FPIES.

Sections du résumé

BACKGROUND BACKGROUND
Food protein-induced enterocolitis syndrome (FPIES) is a rare non-IgE-mediated food allergy that mainly impacts babies and 7toddlers. The exact mechanism of FPIES is not completely understood. By studying the expression of IL-10 and CXCL10 in pediatric FPIES patients, researchers can gain insights into the immune mechanisms underlying this disorder.
METHODS METHODS
Peripheral venous blood was collected and subsequently stabilized with RNA pro. Total RNA was extracted and mRNA levels of CXCL10 and IL-10 was determined with real time PCR.
RESULTS RESULTS
Children with FPIES had significantly higher values than the healthy control group (HC) for CXCL10 while FPIES had a significant lower values than the control group for IL-10.
CONCLUSIONS CONCLUSIONS
Our results show a high production of CXCL10 and a concomitant reduced production of IL-10 in FPIES subjects who have not yet reached tolerance. These data may represent a molecular diagnostic marker for FPIES.

Identifiants

pubmed: 39133968
pii: S1043-4666(24)00223-0
doi: 10.1016/j.cyto.2024.156720
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

156720

Informations de copyright

Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ilaria Galliano (I)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: ilaria.galliano@unito.it.

Paola Montanari (P)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: paola.montanari@unito.it.

Giovanna Monti (G)

Pediatric Allergy Unit, Regina Margherita Children's Hospital, Piazza Polonia 94, Turin, Italy. Electronic address: giovanna.monti@email.it.

Maddalena Dini (M)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: maddalena.dini@unito.it.

Cristina Calvi (C)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: cristina.calvi@unito.it.

Anna Clemente (A)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: anna.clemente@unito.it.

Anna Pau (A)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: anna.pau@unito.it.

Stefano Gambarino (S)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: gambarino.stefano@gmail.com.

Massimiliano Bergallo (M)

Department of Pediatric Sciences and Public Health, University of Turin, Piazza Polonia 94, Turin, Italy. Electronic address: massimiliano.bergallo@unito.it.

Classifications MeSH