Dinastry Pramadita Zakiudin, Anne Dorthea Bjerkenes Rø, Vibeke Videm, Gunnhild Vatne Leirvik, Marte Høen Lein, Torbjørn Øien, Melanie Rae Simpson
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引用次数: 0
Abstract
Background
In the randomised, controlled study Probiotics in the Prevention of Allergy amongst Children in Trondheim (ProPACT), maternal probiotics given from 36 weeks pregnancy until 3 months post-delivery while breastfeeding reduced atopic dermatitis (AD) in the offspring. Previous analysis of T helper (Th) subsets indicated that the preventive effect may be partially mediated through reduced Th22 percentage at 3 months of age.
Objective
To examine the longitudinal effects of maternal probiotics on Th1, Th2, Th17, Th22, and regulatory T cells (Treg) in offspring at 10 days and 2 years of age compared to the previously published 3 months results.
Methods
Pregnant women (n = 415) were randomised to take probiotic milk (Lacticaseibacillus rhamnosus GG, Bifidobacterium animalis subsp. lactis Bb-12 and Lactobacillus acidophilus La-5) or placebo, and their offspring were assessed for AD at 2 years. We analysed the children's blood collected at 10 days (n = 112) and 2 years (n = 156) for Treg and Th subsets using flow cytometry and included the results from the previously analysed 3 months samples (n = 76) in the same study to compare the three timepoints using linear mixed models.
Results
There were no statistically significant differences between T cell populations of the children in the probiotics and placebo groups at 10 days and 2 years.
Conclusion
We previously observed reduced Th22 percentage in the probiotics group at 3 months. However, since the effect was not seen earlier and did not last, it may not be the main reason for AD prevention.
期刊介绍:
Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience.
Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.