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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
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Research Article Gastroenterology Immunology

Synchronization of mothers and offspring promotes tolerance and limits allergy

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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

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Figure 2

A Long-lived diverse Treg population develops in the colon during a pre- and periweaning period.

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A Long-lived diverse Treg population develops in the colon during a pre-...
(A) Naive (CD62L+) T cell and Treg (Foxp3+) populations in the colon LP in early life assessed by flow cytometry. (B) Helios and RORγt+ expression by DOL24 Foxp3+CD4+CD3+ colonic LP cells. (C) Naive (CD62L+) T cell and Treg (Foxp3+) populations in the SI LP in early life assessed by flow cytometry. (D) Absolute number of colonic Foxp3+ (GFP+) cells that express YFP on DOL28 or DOL56 following inducible expression of YFP on DOL24 in Foxp3GFPERT2CreROSAlslYFP mice. (E) viSNE plots of T cells from spleen (spl), mesenteric lymph node (MLN), SI, or Colon LP of DOL56 Foxp3GFPERT2CreROSAlslYFP mice following inducible expression in DOL24 analyzed by GFP and YFP. (F) viSNE plots demonstrating transcription factor expression by colon LP T cells isolated and clustered as in E. Data are presented as the mean ± SEM. *P < 0.05; each dot represents 1 mouse analyzed. B is representative of 1 of 4 mice analyzed; n = 4 or more mice in panels E and F; and offspring from 3 litters were used in A–F. Significance calculated using a 2-tailed Student’s t test in D.

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