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Foetal gluten immunogenic peptides during pregnancy: a new determinant on the coeliac exposome
María de Lourdes Moreno1, María González-Rovira1, Cristina Martínez-Pancorbo2
1Department of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
Insights
First evidence shows fetal exposure to gluten immunogenic peptides (GIP) in utero, correlating with maternal gluten intake. This suggests a prenatal "coeliac exposome" pathway involving fetal swallowing and kidney excretion of GIP in amniotic fluid.
Area of Science:
- Immunology
- Gastroenterology
- Prenatal Medicine
Background:
- Rising coeliac disease incidence prompts investigation into intrauterine and early-life factors.
- The exposome approach considers environmental exposures across the entire lifespan, starting from conception.
- Understanding prenatal exposure to gluten immunogenic peptides (GIP) may alter perspectives on early tolerance or inflammation development.
Purpose of the Study:
- To develop a method for detecting GIP in amniotic fluid (AF).
- To investigate GIP accumulation, excretion dynamics, and fetal exposure via AF swallowing.
- To explore the relationship between maternal gluten intake and fetal GIP exposure.
Main Methods:
- Development of a specific immunoassay for GIP detection in AF.
- Recruitment of 125 pregnant women with varying gluten intake and gestational ages.
- Analysis of GIP levels in AF throughout gestation and assessment of maternal fasting effects.
Main Results:
- GIP was detectable in AF from 16 weeks gestation in women consuming gluten.
- No significant changes in AF GIP levels were observed during gestation.
- Late-pregnancy AF GIP levels were unaffected by maternal fasting, indicating a closed-loop system.
Conclusions:
- This study provides the first evidence of fetal exposure to GIP in utero.
- A positive correlation was established between fetal GIP exposure and maternal gluten intake.
- A novel physiological concept of a closed-loop system involving fetal swallowing and renal excretion of GIP in AF is proposed, contributing to the understanding of the coeliac exposome.
Background:
The increasing incidence of coeliac disease is leading to a growing interest in active search for associated factors, even the intrauterine and early life. The exposome approach to disease encompasses a life course perspective from conception onwards has recently been highlighted. Knowledge of early exposure to gluten immunogenic peptides (GIP) in utero could challenge the chronology of early prenatal tolerance or inflammation, rather than after the infant's solid diet after birth.
Methods:
We developed an accurate and specific immunoassay to detect GIP in amniotic fluid (AF) and studied their accumulates, excretion dynamics and foetal exposure resulting from AF swallowing. One hundred twenty-five pregnant women with different gluten diets and gestational ages were recruited.
Results:
GIP were detectable in AF from at least the 16th gestational week in gluten-consuming women. Although no significant differences in GIP levels were observed during gestation, amniotic GIP late pregnancy was not altered by maternal fasting, suggesting closed-loop entailing foetal swallowing of GIP-containing AF and subsequent excretion via the foetal kidneys.
Conclusions:
The study shows evidence, for the first time, of the foetal exposure to gluten immunogenic peptides and establishes a positive correlation with maternal gluten intake. The results obtained point to a novel physiological concept as they describe a plausible closed-loop circuit entailing foetal swallowing of GIP contained in AF and its subsequent excretion through the foetal kidneys. The study adds important new information to understanding the coeliac exposome.
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