# T‐Cell Populations in Infancy After Maternal Probiotic Supplementation to Prevent Atopic Dermatitis

**Authors:** Dinastry Pramadita Zakiudin, Anne Dorthea Bjerkenes Rø, Vibeke Videm, Gunnhild Vatne Leirvik, Marte Høen Lein, Torbjørn Øien, Melanie Rae Simpson

PMC · DOI: 10.1002/clt2.70161 · Clinical and Translational Allergy · 2026-02-26

## TL;DR

A study found that maternal probiotics during pregnancy and breastfeeding did not significantly affect T-cell populations in infants at 10 days or 2 years, suggesting the earlier observed Th22 reduction at 3 months may not be the main reason for preventing atopic dermatitis.

## Contribution

The study extends the analysis of maternal probiotics' effects on T-cell subsets in offspring to 2 years of age, revealing that the earlier Th22 reduction may not be a lasting mechanism for AD prevention.

## Key findings

- Maternal probiotics did not significantly alter T-cell populations in offspring at 10 days or 2 years of age.
- The previously observed reduction in Th22 cells at 3 months did not persist at later timepoints.
- The lack of consistent T-cell changes suggests Th22 reduction may not be the primary mechanism for AD prevention.

## Abstract

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.

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.

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.

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.

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.

## Linked entities

- **Diseases:** atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Genes:** FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, IL17C (interleukin 17C) [NCBI Gene 27189] {aka CX2, IL-17C}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL7R (interleukin 7 receptor) [NCBI Gene 3575] {aka CD127, CDW127, IL-7R-alpha, IL-7Ralpha, IL7RA, IL7Ralpha}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** Allergy-related disease (MESH:D000077733), Dermatitis (MESH:D003872), itchy rash (MESH:D005076), Asthma (MESH:D001249), water loss (MESH:D000069578), impaired night sleep (MESH:D012893), skin lesions (MESH:D012871), inflammation (MESH:D007249), upper respiratory infection (MESH:D012141), skin barrier defects (MESH:D012868), AD (MESH:D003876), epidermal hyperplasia (MESH:D006965), Allergy (MESH:D004342), wheeze (MESH:D012135), cough (MESH:D003371), Eczema (MESH:D004485)
- **Chemicals:** PMA (MESH:D013755), brefeldin A (MESH:D020126), CO2 (MESH:D002245), ionomycin (MESH:D015759), monensin (MESH:D008985), Cy-7 (-)
- **Species:** Limosilactobacillus reuteri (species) [taxon 1598], Lactobacillus sp. A5 (species) [taxon 1770019], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945665/full.md

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Source: https://tomesphere.com/paper/PMC12945665