Evidence map›Paper›PMID 32759496›Full record

ArticleJCI insight2020

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 and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Dietary Antigen Interaction with Intestinal Epithelial Cells.Current allergy and asthma reports · 2026
    Review
  7. Review
  8. Review
  9. Early life infection withGut microbes · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Intergenerational protective anti-gut commensal immunoglobulin G originates in early life.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Kathryn A KnoopDepartment of Internal Medicine and.
Keely G McDonaldDepartment of Internal Medicine and.
Paige E CoughlinDepartment of Internal Medicine and.
Devesha H KulkarniDepartment of Internal Medicine and.
Jenny K GustafssonDepartment of Internal Medicine and.
Brigida RusconiDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Vini JohnDepartment of Internal Medicine and.
I Malick NdaoDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Avraham BeigelmanDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Misty GoodDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Barbara B WarnerDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Charles O ElsonDepartment of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
Chyi-Song HsiehDepartment of Internal Medicine and.
Simon P HoganMary H. Weiser Food Allergy Center, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
Phillip I TarrDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Rodney D NewberryDepartment of Internal Medicine and.
Washington University in St. Louis · USTel Aviv University · ILUniversity of Alabama at Birmingham · USUniversity of Michigan · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
INNATE AND ADAPTIVE MICROBIAL IMMUNITY IN IBDP01DK071176 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ELSON, CHARLES O · 2005 to 2014
$12.5M
Mucosal Immune Defense Mechanisms of the Urinary BladderU01AI095542 · NIAID · WASHINGTON UNIVERSITY · PI COLONNA, MARCO, HULTGREN, SCOTT J. · 2011 to 2020
$9.8M
Viral Discovery in Rheumatoid ArthritisP30AR048335 · NIAMS · WASHINGTON UNIVERSITY · PI WEIHL, CONRAD C · 2001 to 2015
$8.9M
GOBLET CELLS IN INTESTINAL IMMUNE HOMEOSTATSISR01DK097317 · NIDDK · WASHINGTON UNIVERSITY · PI NEWBERRY, RODNEY D · 2012 to 2025
$5.6M
The Role of Route of Entry by Bacterial Antigens on Colonic T Cell ResponsesR01AI136515 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S, NEWBERRY, RODNEY D · 2018 to 2022
$2.8M
ROLE OF STRESS IN GUT IMMUNE INTERACTIONS WITH COMMENSAL BACTERIAR01AI140755 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S, NEWBERRY, RODNEY D · 2018 to 2021
$2.6M
Food Allergy and Goblet Cell Antigen PassagesR01AI112626 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOGAN, SIMON PATRICK, NEWBERRY, RODNEY D · 2015 to 2019
$2.4M
GUT SPECIFIC AND TIME-LIMITED EVENTS IN EARLY LIFE PROMOTING TOLERANCEU01AI131342 · NIAID · WASHINGTON UNIVERSITY · PI NEWBERRY, RODNEY D, TARR, PHILLIP I · 2017 to 2021
$2.2M
Modulation of the Intestinal Immune Response in Necrotizing EnterocolitisR01DK118568 · NIDDK · WASHINGTON UNIVERSITY · PI GOOD, MISTY L · 2018 to 2022
$1.8M
S1P as regulator of neonatal mucosal immune development and injuryK01DK125606 · NIDDK · WASHINGTON UNIVERSITY · PI RUSCONI, BRIGIDA AGNESE · 2020 to 2024
$679k
NCI NIH HHS P30 CA091842NIAID NIH HHS R01 AI112626NIAID NIH HHS R01 AI136515NIAID NIH HHS R01 AI140755NIAID NIH HHS U01 AI095542NIAID NIH HHS U01 AI131342NIAMS NIH HHS P30 AR048335NIDDK NIH HHS K01 DK109006NIDDK NIH HHS K01 DK125606NIDDK NIH HHS K08 DK101608NIDDK NIH HHS P01 DK071176NIDDK NIH HHS P30 DK052574NIDDK NIH HHS R01 DK097317NIDDK NIH HHS R01 DK118568NIDDK NIH HHS R03 DK111473
6 · The paper itself

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.

Indexed as

AllergensAnimalsAnimals, NewbornAntigen-Presenting CellsColonFemaleFood HypersensitivityImmune ToleranceImmunoglobulin GMiceMice, Inbred C57BLMilkMothersOvalbuminTh2 CellsT-Lymphocytes, RegulatoryAllergensImmunoglobulin GOvalbuminAllergyGastroenterologyImmunologyTolerance

Identifiers

PMID32759496
PMCPMC7455068
OpenAlexW3047091444

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.