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Published on: August 7, 2017
Gut microbiome in the first 1000 days and risk for childhood food allergy
Erin C Davis1, Cynthia L Monaco2, Richard Insel1
1Division of Allergy and Immunology, Center for Food Allergy, Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Golisano Children's Hospital, Rochester, New York.
Insights
The infant gut microbiome
Area of Science:
- Microbiome Research
- Immunology
- Pediatric Allergy
Background:
- Food allergy (FA) is a growing public health concern in early childhood.
- The gut microbiome plays a critical role in immune system development and tolerance.
- Understanding the interplay between the microbiome and FA is crucial for prevention and treatment strategies.
Purpose of the Study:
- To review current research on the gut microbiome's role in childhood food allergy.
- To explore how host-microbiome interactions influence oral tolerance.
- To identify key microbial and host factors involved in FA pathogenesis.
Main Methods:
- Systematic literature search of PubMed for studies on FA, atopic disease, and gut microbiome (post-2015).
- Prioritization of human studies focusing on infant gut bacteriome, virome, and FA development.
- Inclusion of prenatal microbiome studies and preclinical research for comprehensive analysis.
Main Results:
- Infants with FA showed reduced Bifidobacterium and Clostridia, and a less mature microbiome.
- The early microbiome may protect against FA via anti-inflammatory metabolites and T regulatory cell induction.
- Maternal microbiome during pregnancy is linked to childhood FA risk, possibly through metabolite transfer.
Conclusions:
- Maternal and infant microbiomes within the first 1000 days significantly impact FA risk.
- Proposed mechanisms involve microbial metabolites and immune cell modulation.
- Large, longitudinal studies with multi-omic analyses are needed to elucidate host-microbe interactions in FA.
Objective:
To summarize recent data on the association between gut microbiome composition and food allergy (FA) in early childhood and highlight potential host-microbiome interactions that reinforce or abrogate oral tolerance.
Data Sources:
PubMed search of English-language articles related to FA, other atopic disease, and the gut microbiome in pregnancy and early childhood.
Study Selections:
Human studies published after 2015 assessing the relationship between the gut bacteriome and virome in the first 2 years of life and FA or food sensitization development in early childhood were prioritized. Additional human studies conducted on the prenatal gut microbiome or other atopic diseases and preclinical studies are also discussed.
Results:
Children who developed FA harbored lower abundances of Bifidobacterium and Clostridia species and had a less mature microbiome during infancy. The early bacterial microbiome protects against FA through production of anti-inflammatory metabolites and induction of T regulatory cells and may also affect FA risk through a role in trained immunity. Infant enteric phage communities are related to childhood asthma development, though no data are available for FA. Maternal gut microbiome during pregnancy is associated with childhood FA risk, potentially through transplacental delivery of maternal bacterial metabolites, though human studies are lacking.
Conclusion:
The maternal and infant microbiomes throughout the first 1000 days of life influence FA risk through a number of proposed mechanisms. Further large, longitudinal cohort studies using taxonomic, functional, and metabolomic analysis of the bacterial and viral microbiomes are needed to provide further insight on the host-microbe interactions underlying FA pathogenesis in childhood.
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