Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Synchronization of mothers and offspring promotes tolerance and limits allergy
Kathryn A. Knoop, Keely G. McDonald, Paige E. Coughlin, Devesha H. Kulkarni, Jenny K. Gustafsson, Brigida Rusconi, Vini John, I. Malick Ndao, Avraham Beigelman, Misty Good, Barbara B. Warner, Charles O. Elson, Chyi-Song Hsieh, Simon P. Hogan, Phillip I. Tarr, Rodney D. Newberry
Kathryn A. Knoop, Keely G. McDonald, Paige E. Coughlin, Devesha H. Kulkarni, Jenny K. Gustafsson, Brigida Rusconi, Vini John, I. Malick Ndao, Avraham Beigelman, Misty Good, Barbara B. Warner, Charles O. Elson, Chyi-Song Hsieh, Simon P. Hogan, Phillip I. Tarr, Rodney D. Newberry
View: Text | PDF
Research Article Gastroenterology Immunology

Synchronization of mothers and offspring promotes tolerance and limits allergy

  • Text
  • PDF
Abstract

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.

Authors

Kathryn A. Knoop, Keely G. McDonald, Paige E. Coughlin, Devesha H. Kulkarni, Jenny K. Gustafsson, Brigida Rusconi, Vini John, I. Malick Ndao, Avraham Beigelman, Misty Good, Barbara B. Warner, Charles O. Elson, Chyi-Song Hsieh, Simon P. Hogan, Phillip I. Tarr, Rodney D. Newberry

×

Figure 3

Dietary antigen is delivered to the colonic immune system during a preweaning period, results in the induction of tolerance, and generates a population of long-lived dietary antigen–specific pTregs.

Options: View larger image (or click on image) Download as PowerPoint
Dietary antigen is delivered to the colonic immune system during a prewe...
(A) Luminal antigen presentation capacity of SI and colon LP-APCs isolated from mice receiving dietary Ova in early life as assessed by the increase in Ova-specific OTII T cells after 72 hours of coculture. (B) Dietary Ova was given to mice for 10-day intervals throughout life, and tolerance was evaluated following Ova immunization and challenge, as assessed by footpad swelling. (C) Absolute number of Foxp3+ Ova-specific OTII cells in the SI or colon LP 1 or 8 weeks following transfer into DOL16 or DOL56 mice that were given Ova in drinking water for 7 days. (D) Percentage of colonic OTII T cells that are Foxp3+ and RORγt+ 8 weeks following transfer into DOL16 mice and 1 week of Ova in drinking water. Data are presented as the mean ± SEM, *P < 0.05; each point represents an individual mouse. Offspring were from 2 litters per condition and/or time point. Significance was calculated using 2-tailed Student’s t test in A, C, D. One-way ANOVA with a Dunnett’s post hoc test was used in B.

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts