Adipose Tissue Immunomodulation and Treg/Th17 Imbalance in the Impaired Glucose Metabolism of Children with Obesity.

Th17 Treg adipose tissue-associated inflammation childhood obesity glucose metabolism disorders

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
27 Jun 2021
Historique:
received: 20 05 2021
revised: 18 06 2021
accepted: 25 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

In the last few decades, obesity has increased dramatically in pediatric patients. Obesity is a chronic disease correlated with systemic inflammation, characterized by the presence of CD4 and CD8 T cell infiltration and modified immune response, which contributes to the development of obesity related diseases and metabolic disorders, including impaired glucose metabolism. In particular, Treg and Th17 cells are dynamically balanced under healthy conditions, but imbalance occurs in inflammatory and pathological states, such as obesity. Some studies demonstrated that peripheral Treg and Th17 cells exhibit increased imbalance with worsening of glucose metabolic dysfunction, already in children with obesity. In this review, we considered the role of adipose tissue immunomodulation and the potential role played by Treg/T17 imbalance on the impaired glucose metabolism in pediatric obesity. In the patient care, immune monitoring could play an important role to define preventive strategies of pediatric metabolic disease treatments.

Identifiants

pubmed: 34199040
pii: children8070554
doi: 10.3390/children8070554
pmc: PMC8305706
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Stefania Croce (S)

Immunology and Transplantation Laboratory, Pediatric Hematology Oncology Unit, Cell Factory, Department of Maternal and Children's Health, Fondazione IRCCS Policlinico S. Matteo, 27100 Pavia, Italy.

Maria Antonietta Avanzini (MA)

Immunology and Transplantation Laboratory, Pediatric Hematology Oncology Unit, Cell Factory, Department of Maternal and Children's Health, Fondazione IRCCS Policlinico S. Matteo, 27100 Pavia, Italy.

Corrado Regalbuto (C)

Pediatric Unit, Department of Maternal and Children's Health, Fondazione IRCCS Policlinico S. Matteo and University of Pavia, 27100 Pavia, Italy.

Erika Cordaro (E)

Immunology and Transplantation Laboratory, Pediatric Hematology Oncology Unit, Cell Factory, Department of Maternal and Children's Health, Fondazione IRCCS Policlinico S. Matteo, 27100 Pavia, Italy.

Federica Vinci (F)

Pediatric Unit, Department of Maternal and Children's Health, Fondazione IRCCS Policlinico S. Matteo and University of Pavia, 27100 Pavia, Italy.

Gianvincenzo Zuccotti (G)

Department of Biomedical and Clinical Science, "Luigi Sacco", University of Milan, 20157 Milan, Italy.
Pediatric Department, "Vittore Buzzi" Children's Hospital, 20154 Milano, Italy.

Valeria Calcaterra (V)

Pediatric Department, "Vittore Buzzi" Children's Hospital, 20154 Milano, Italy.
Pediatrics and Adolescentology Unit, Department of Internal Medicine, University of Pavia, 27100 Pavia, Italy.

Classifications MeSH