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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 4

Desynchronizing pups and dams impairs the development of a long-lived population of colonic Tregs that can be specific for dietary antigen.

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Desynchronizing pups and dams impairs the development of a long-lived po...
(A) Population of colonic LP Tregs in cross-fostered mice by DOL. (B) Total Treg population in cross-fostered mice on DOL240. (C) Ratio of RORγt+ pTregs (Helios–) to tTregs (Helios+) in the colonic LP of cross-fostered mice at DOL28 or DOL240. (D) viSNE plots of colonic LP T cells isolated from cross-fostered mice on DOL80 stained for transcription factors as in Supplemental Figure 6; arrows denote missing population following ACF. (E) Number of colon LP CD4+ T cells expressing YFP and or GFP in DOL56 cross-fostered Foxp3GFPERT2CreROSAlslYFP mice following inducible expression on DOL24. (F) Absolute number of Ova-specific OTII T cells in the colon LP of cross-fostered mice receiving OTII T cells on DOL16, given Ova in drinking water, and evaluated 1 week later. Data are presented as the mean ± SEM, *P < 0.05; each dot represents analysis of 1 mouse. n = at least 4 mice per group; offspring from 3 litters per condition and/or time point were used in A–F. D is representative of 3 independent pooling analysis with 2 mice per group. Significance calculated using 2-way ANOVA with a Dunnett’s post hoc test in A and 1-way ANOVA with a Dunnett’s post hoc test in B, C, E, and F.

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