Related Experiment Video
Updated: Sep 6, 2025

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Household size, T regulatory cell development, and early allergic disease: a birth cohort study
Anne-Louise Ponsonby1,2, Fiona Collier3, Martin O'Hely2,3
1The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
Insights
Children from larger households show fewer allergies. Larger household size correlates with increased T regulatory cell (Treg) development, which is linked to reduced allergy risk in infants.
Area of Science:
- Immunology
- Environmental Health
- Pediatrics
Background:
- Growing evidence suggests a link between household size and reduced allergic disease in children.
- T regulatory cell (Treg) development is a potential mechanism, but longitudinal studies are lacking.
Purpose of the Study:
- To investigate the association between prenatal/postnatal environmental factors and Treg development.
- To determine if serial Treg measurements predict allergic outcomes in infants at one year of age.
Main Methods:
- A birth cohort of 1074 infants with early life factor data.
- Longitudinal measurement of naïve Treg (nTreg) and activated Treg (aTreg) cell populations.
- Assessment of allergic status including polysensitization, food allergy, eczema, and wheeze at 12 months.
Main Results:
- Larger households (≥3 residents) were associated with higher longitudinal nTreg proportions.
- Higher nTreg at birth correlated with a reduced risk of infant allergic outcomes.
- Childcare attendance and breastfeeding were linked to increased longitudinal nTreg proportions.
Conclusions:
- Prenatal and postnatal microbial factors influence nTreg and aTreg development.
- Larger household size promotes nTreg development, which is associated with decreased allergic sensitization and disease.
Background:
Children born to larger households have less allergic disease. T regulatory cell (Treg) development may be a relevant mechanism, but this has not been studied longitudinally.
Objective:
We aim to (i) describe how prenatal and postnatal environmental factors are associated with Treg development and (ii) investigate whether serial Treg measures predict allergic outcomes at 1 year of age.
Methods:
A birth cohort (n = 1074) with information on prenatal and postnatal early life factors. Both naïve Treg (nTreg) and activated Treg (aTreg) cell populations (as a proportion of CD4+ T cells) were available in 463 infants at birth (cord blood), 600 at 6 months, and 675 at 12 months. 191 infants had serial measures. Measures of allergic status at 12 months were polysensitization (sensitization to 2 or more allergens), clinically proven food allergy, atopic eczema, and atopic wheeze.
Results:
Infants born to larger households (3 or more residents) had higher longitudinal nTreg proportions over the first postnatal year with a mean difference (MD) of 0.67 (95% CI 0.30-1.04)%. Higher nTreg proportions at birth were associated with a reduced risk of infant allergic outcomes. Childcare attendance and breastfeeding were associated with higher longitudinal nTreg proportions (MD 0.48 (95% CI 0.08-0.80)%.
Conclusion:
Multiple prenatal and postnatal microbial factors are associated with nTreg and aTreg development. Larger household size was associated with higher nTreg at birth which in turn was associated with reduced allergic sensitization and disease at 12 months of age.
More Related Videos
Related Concept Videos
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Allergic Reactions
Asthma-II: Pathophysiology and Classification
Additionally, environmental and genetic factors play crucial roles in determining an individual's susceptibility to asthma and the severity of their condition.
Critical processes in asthma pathophysiology include:

