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Published on: August 7, 2017
Early markers of allergic disease in a primary prevention study using probiotics: 2.5-year follow-up phase
S L Prescott1, J Wiltschut, A Taylor
1School of Paediatrics and Child Health, University of Western Australia, Perth, WA, Australia.
Insights
The Lactobacillus acidophilus probiotic strain LAFTI L10 did not impact allergy outcomes in children. Early immune differences, including regulatory T-cell markers, were observed in allergic children.
Area of Science:
- Immunology
- Allergy Research
- Microbiome Studies
Background:
- Previous research indicated a potential increased risk of allergen sensitization at one year of age with Lactobacillus acidophilus probiotic strain LAFTI L10 supplementation during infancy.
- This study aimed to evaluate the long-term effects of this probiotic on allergic outcomes.
Purpose of the Study:
- To assess the impact of Lactobacillus acidophilus probiotic strain LAFTI L10 on allergic disease development and allergen sensitization up to 2.5 years of age.
- To investigate the relationship between early immune function at 6 months and subsequent allergic outcomes.
Main Methods:
- A cohort of 153 children from an initial prevention trial were followed up to 2.5 years of age.
- Clinical outcomes (dermatitis, allergic disease, sensitization) and immune markers (T-cells, cytokine responses) were assessed in relation to probiotic supplementation and early immune function.
Main Results:
- Probiotic supplementation did not reduce the incidence of dermatitis or other allergic diseases by 2.5 years.
- Inhalant sensitization at 2.5 years was associated with higher regulatory T-cell populations and FOXP3 levels at 6 months.
- Children with dermatitis exhibited altered innate immune responses and lower toll-like receptor 4 responses at 6 months.
Conclusions:
- The Lactobacillus acidophilus LAFTI L10 probiotic strain showed no significant long-term benefit for allergy outcomes.
- Early differences in immune function, including regulatory T-cell markers and innate immunity, were identified in children who developed allergies.
Background:
We previously reported that a Lactobacillus acidophilus probiotic strain (LAFTI) L10/LAVRI-A1) given for the first 6 months of life increased the risk of allergen sensitization at 1 year of age.
Methods:
To assess the effects on subsequent allergic outcomes, 153 children from the initial prevention cohort (n = 178) were reviewed at 2.5 years of age. Clinical outcomes were assessed in relation to (i) probiotic supplementation; and (ii) immune function previously assessed at 6 months of age.
Results:
Supplementation with this probiotic did not reduce the risk of dermatitis at 2.5 years (31/74, 42%) compared with that in placebo group (25/76, 34%). There was no significant reduction in any other allergic disease or allergen sensitization. Inhalant sensitization at 2.5 years (n = 29) was associated with higher proportions of circulating CD4+ CD25+ regulatory T-cell populations (P = 0.005) and higher allergen-induced FOXP3 levels (P = 0.003) at 6 months. This was also seen in children with dermatitis. Children with dermatitis at 2.5 years also had significantly lower toll-like receptor 4 lipopolysaccharide responses at 6 months of age (IL-12 P = 0.04, IL-6 P = 0.039) and lower polyclonal (PHA) responses (IFN-gamma P = 0.005, IL-10 P = 0.001, and IL-6 P = 0.001). Children who had previously received the probiotic had fewer gastrointestinal infections in the preceding 18 months (P = 0.023).
Conclusion:
The LAFTI L10 probiotic strain did not have any significant effect on allergy outcomes. Allergic children showed a number of early differences in immune function including altered regulatory T-cell markers and innate immune function.
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