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RecruitingNCT07744373Updated Aug 4, 2026

Tregs and miRNAs in Breast Milk: Effects on Infant Food Tolerance

An observational study in Immune Tolerance and Food Tolerance, sponsored by Istanbul University. Recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 0 Days to 9 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by Istanbul University · Observational

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
25
Ages
0 Days to 9 Months
Sex
All
01

Study summary

This prospective observational study aims to identify and characterize immunoregulatory microRNAs (miRNAs) associated with regulatory T cells (Tregs) in human breast milk and to evaluate their temporal expression patterns. Breast milk samples will be collected longitudinally, including colostrum, transitional milk (days 10-15), and mature milk at 1, 4, 6, and/or 9 months postpartum. The study will investigate miRNAs that may influence the development and function of Treg cells and assess changes in their expression over time. In addition, a single blood sample will be obtained from infants during routine clinical visits (6-9 months postpartum) to analyze Treg-related miRNAs and target genes and to evaluate their relationship with breast milk components. The study also aims to explore the association between breast milk miRNAs, Treg-related immune mechanisms, and the development of infant food tolerance.

Read the detailed description

Breast milk contains microRNAs (miRNAs) that contribute to the maturation of the infant immune system by influencing immune cell development, inflammatory mediator secretion, and maintenance of immunological homeostasis. Certain miRNAs, such as miR-92 and miR-17, play a role in B- and T-cell maturation, while miRNA-10a is associated with regulatory T cells (Tregs), which can modulate food allergic responses. This study aims to identify immunoregulatory Treg-associated miRNAs in breast milk, particularly those involved in the development and function of Treg cells; to analyze their expression in colostrum, transitional milk, and mature breast milk; to investigate their effects on Treg cells; and to examine the relationship between food tolerance and miRNA-Treg interactions.

Laboratory analyses will be conducted on maternal breast milk and infant blood samples. Breast milk samples will be manually expressed between 09:00 and 14:00 into sterile collection containers, with 7-10 mL collected per session. Five milliliters of each sample will be transferred into Eppendorf tubes and transported on ice within 30 minutes for molecular analysis. Each sample will be aliquoted into sterile 2 mL cryotubes, flash-frozen, and stored at -80°C until RNA isolation. The remaining 2-5 mL of each breast milk sample will be transported on ice within 30 minutes for immunologic and cytometric analyses. Infant blood samples obtained during routine follow-up visits will be analyzed for Treg-associated miRNAs and their target gene expression to evaluate correlations with maternal breast milk miRNA profiles and infant immune tolerance.

All laboratory analyses will be conducted using standard equipment and procedures in certified Genetics and Immunology laboratories. Through this approach, the study will examine longitudinal changes in Treg-associated miRNAs in breast milk, their correlation with infant immune parameters, and their potential role in promoting immune tolerance and preventing food allergy development. The results are expected to provide insights into early-life immune programming and may inform novel therapeutic interventions and preventive strategies.

02

Conditions studied

  • Immune Tolerance
  • Food Tolerance

Keywords

  • Food Tolerance
  • breast milk
  • Immune Tolerance
03

In context

Lead sponsor

Istanbul University is the lead sponsor of 496 studies on the registry; 79 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Days to 9 Months
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

This study will include healthy lactating mothers and their term infants (≥37 weeks gestation) who are followed at Istanbul University, Istanbul Medical Faculty, Department of Social Pediatrics, Well Child Outpatient Clinic or the Esencan Hospital Outpatient Clinic. Infants must be exclusively breastfed for the first 6 months. Mothers and infants must be willing to provide breast milk and infant blood samples at specified time points and provide informed consent. Infants with chronic illnesses or major congenital anomalies, and mothers unable or unwilling to comply with study procedures, will be excluded.

Inclusion criteria

  1. Lactating mothers and their infants attending the Child Health and Diseases Clinic at Istanbul University Faculty of Medicine, or the Child Health and Diseases Clinic at Esencan Hospital.
  2. Infants who are exclusively breastfed for the first 6 months.
  3. Mothers willing to provide breast milk samples at multiple time points (colostrum, transitional milk, and mature milk at 1, 4, 6, and/or 9 months postpartum).
  4. Infants aged 0-9 months, born at term (≥37 weeks gestation) with no major congenital anomalies or chronic illnesses.
  5. Mothers and infants who provide informed consent for participation in the study.

Exclusion criteria

Exclusion Criteria:

  1. Infants who are not exclusively breastfed for the first 6 months.
  2. Infants with chronic illnesses or diagnosed immunodeficiency, metabolic, or gastrointestinal disorders.
  3. Mothers who are unable or unwilling to provide informed consent.
  4. Mothers with chronic illnesses or immunological disorders that may affect breast milk composition.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
25 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Expression Levels of Treg-Associated miRNAs in Breast Milk

    Quantitative analysis of regulatory T cell (Treg)-associated microRNA (miRNA) expression levels in breast milk samples.

    Time frame: Colostrum (day 0-7), days 10-15 (transitional milk), and at 1, 4, 6, and 9 months postpartum

07

Study locations

2 of 2 sites recruiting
  • Child Health and Diseases Clinic, Esencan Hospital
    Istanbul, Turkey (Türkiye)
    • Özden Durmuş Gönültaş, MD · Contact · ozdengnlts@gmail.com · 905073121218
    • Özden Durmuş Gönültaş, MD · Sub investigator
    Recruiting
  • İstanbul University İstanbul Medical Faculty Department of Pediatrics Division of Social Pediatrics
    Istanbul, Turkey (Türkiye)
    • Gonca Keskindemirci, MD, PhD · Contact · keskindemirci@hotmail.com · 0905324934651
    • Gonca Keskindemirci, Prof · Principal investigator
    • Gülbin E Gökçay, Prof · Principal investigator
    • Günnur Deniz, Prof · Principal investigator
    • Asuman Gedikbaşı, Prof · Principal investigator
    • Birsen Karaman, Prof · Principal investigator
    • Bilge Ş Selçuk, Assoc Prof · Principal investigator
    • Gizem Kara Elitok, Assoc Prof · Sub investigator
    • Özden Durmuş Gönültaş, MD · Sub investigator
    • Ebru Kılıç · Sub investigator
    • Ayşenur Kökoğlu · Sub investigator
    • Suzin Tatonyan · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07744373
Lead sponsor
Istanbul University
Responsible party
Gonca Keskindemirci (Professor of Pediatrics, Istanbul University) — Principal investigator
First posted
Aug 4, 2026
Start date
Oct 1, 2025
Primary completion
Sep 30, 2026 (estimated)
Completion
Sep 30, 2026 (estimated)
Last update
Aug 4, 2026

Study contacts

Gonca Keskindemirci, MD, PhD
Contact
keskindemirci@hotmail.com
0905324934651
View the source record on ClinicalTrials.gov ↗

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