Reduced Th22 cell proportion and prevention of atopic dermatitis in infants following maternal probiotic

A D B Rø1,2, M R Simpson1, T B Rø3,4,5

  • 1Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.

Insights

Maternal probiotic supplementation reduced atopic dermatitis (AD) in children by lowering Th22 cells. This study investigated how probiotics impact T helper cells, potentially explaining their protective effect against AD.

Area of Science:

  • Immunology
  • Microbiome research
  • Pediatric allergy

Background:

  • Maternal probiotic supplementation in the Probiotics in the Prevention of Allergy among Children in Trondheim (ProPACT) study reduced offspring atopic dermatitis (AD).
  • The current study hypothesized that T helper (Th) cell shifts mediate this preventive effect.

Purpose of the Study:

  • To determine if maternal probiotics alter Th cell proportions in infants.
  • To investigate if these Th cell changes mediate the protective effect of probiotics against AD.

Main Methods:

  • 415 pregnant women received a probiotic combination (Lactobacillus rhamnosus GG, Bifidobacterium animalis subsp. lactis Bb-12, Lactobacillus acidophilus La-5) or placebo.
  • Offspring were monitored for AD for 2 years.
  • Peripheral blood from 3-month-old infants was analyzed for regulatory T cells and Th subsets (Th1, Th2, Th9, Th17, Th22).

Main Results:

  • Infants in the probiotic group showed a reduced proportion of Th22 cells compared to the placebo group (0.038% vs 0.064%, P=.009).
  • This reduction was observed even in infants who did not develop AD.
  • Children who developed AD had increased Th22 cells compared to those who did not (0.090% vs 0.044%, P<.001).

Conclusions:

  • Perinatal maternal probiotic supplementation with LGG, Bb-12, and La-5 decreased Th22 cell proportions in 3-month-old infants.
  • This reduction in Th22 cells may partially explain the observed preventive effect of probiotics on atopic dermatitis.
Abstract