Synchronization of mothers and offspring promotes tolerance and limits allergy.
Allergens
/ immunology
Animals
Animals, Newborn
Antigen-Presenting Cells
/ immunology
Colon
/ immunology
Female
Food Hypersensitivity
/ immunology
Immune Tolerance
/ immunology
Immunoglobulin G
/ blood
Mice
Mice, Inbred C57BL
Milk
/ immunology
Mothers
Ovalbumin
/ immunology
T-Lymphocytes, Regulatory
/ immunology
Th2 Cells
/ immunology
Weaning
Allergy
Gastroenterology
Immunology
Tolerance
Journal
JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073
Informations de publication
Date de publication:
06 08 2020
06 08 2020
Historique:
received:
06
03
2020
accepted:
24
06
2020
entrez:
8
8
2020
pubmed:
8
8
2020
medline:
1
6
2021
Statut:
epublish
Résumé
Allergic disorders, characterized by Th2 immune responses to environmental substances, are increasingly common in children in Western societies. Multiple studies indicate that breastfeeding, early complementary introduction of food allergens, and antibiotic avoidance in the first year of life reduces allergic outcomes in at-risk children. Why the benefit of these practices is restricted to early life is largely unknown. We identified a preweaning interval during which dietary antigens are assimilated by the colonic immune system. This interval is under maternal control via temporal changes in breast milk, coincides with an influx of naive T cells into the colon, and is followed by the development of a long-lived population of colonic peripherally derived Tregs (pTregs) that can be specific for dietary antigens encountered during this interval. Desynchronization of mothers and offspring produced durable deficits in these pTregs, impaired tolerance to dietary antigens introduced during and after this preweaning interval, and resulted in spontaneous Th2 responses. These effects could be rescued by pTregs from the periweaning colon or by Tregs generated in vitro using periweaning colonic antigen-presenting cells. These findings demonstrate that mothers and their offspring are synchronized for the development of a balanced immune system.
Identifiants
pubmed: 32759496
pii: 137943
doi: 10.1172/jci.insight.137943
pmc: PMC7455068
doi:
pii:
Substances chimiques
Allergens
0
Immunoglobulin G
0
Ovalbumin
9006-59-1
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIAID NIH HHS
ID : U01 AI131342
Pays : United States
Organisme : NIDDK NIH HHS
ID : K01 DK109006
Pays : United States
Organisme : NIDDK NIH HHS
ID : P01 DK071176
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI112626
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI095542
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK097317
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI136515
Pays : United States
Organisme : NIDDK NIH HHS
ID : R03 DK111473
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR048335
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA091842
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI140755
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK118568
Pays : United States
Organisme : NIDDK NIH HHS
ID : K01 DK125606
Pays : United States
Organisme : NIDDK NIH HHS
ID : K08 DK101608
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK052574
Pays : United States
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