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Published on: January 27, 2019
Probiotic stool secretory immunoglobulin A modulation in children with gastroenteritis: a randomized clinical trial
Stephen B Freedman1,2, Rachael Horne3, Kathene Johnson-Henry3
1Sections of Pediatric Emergency Medicine and Gastroenterology, Department of Pediatrics, Alberta Children's Hospital, Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.
Insights
A Lactobacillus probiotic did not increase stool secretory immunoglobulin A (sIgA) in children with acute gastroenteritis (AGE). This study found no immunomodulatory benefits from the probiotic compared to placebo.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Microbiome Research
Background:
- The Probiotic Regimen for Outpatient Gastroenteritis Utility of Treatment (PROGUT) study found no clinical benefits of probiotics for acute gastroenteritis (AGE) in children.
- The PROGUT study did not assess potential immunomodulatory effects of probiotic use.
Purpose of the Study:
- To investigate the impact of a Lactobacillus rhamnosus/helveticus probiotic on stool secretory immunoglobulin A (sIgA) concentrations in children with AGE.
- To compare changes in sIgA levels between children receiving a probiotic and those receiving a placebo.
Main Methods:
- An ancillary, multicenter, randomized, double-blinded, placebo-controlled study.
- Children with AGE received a 5-day course of either probiotic or placebo.
- Stool specimens were collected at baseline, day 5, and day 28 to measure sIgA concentrations.
Main Results:
- No significant difference in median stool sIgA concentrations was observed between the probiotic and placebo groups at any time point (day 0, 5, or 28).
- Analysis of sIgA changes from baseline to day 5, and day 5 to day 28, showed no treatment allocation effect.
- While sIgA levels decreased from day 5 to day 28 in both groups, there was no difference between groups.
Conclusions:
- The administration of Lactobacillus rhamnosus/helveticus did not alter stool sIgA concentrations in children with acute gastroenteritis.
- The findings suggest no immunomodulatory effect of this probiotic on gut sIgA levels in this pediatric population.
- The study was registered on clinicaltrials.gov (NCT01853124).
Background:
We previously conducted the Probiotic Regimen for Outpatient Gastroenteritis Utility of Treatment (PROGUT) study, which identified no improvements in children with acute gastroenteritis (AGE) administered a probiotic. However, the aforementioned study did not evaluate immunomodulatory benefits.
Objectives:
The object of this study was to determine if stool secretory immunoglobulin A (sIgA) concentrations in children with AGE increase more among participants administered a Lactobacillus rhamnosus/helveticus probiotic compared with those administered placebo.
Methods:
This a priori planned multicenter, randomized, double-blinded, placebo-controlled ancillary study enrolled children presenting for emergency care who received a 5-d probiotic or placebo course. Participants submitted stool specimens on days 0, 5, and 28. The primary endpoint was the change in stool sIgA concentrations on day 5 compared with baseline.
Results:
A total of 133 (n = 66 probiotic, 67 placebo) of 886 PROGUT participants (15.0%) provided all 3 specimens. Median stool sIgA concentrations did not differ between the probiotic and placebo groups at any of the study time points: day 0 median (IQR): 1999 (768, 4071) compared with 2198 (702, 5278) (P = 0.27, Cohen's d = 0.17); day 5: 2505 (1111, 5310) compared with 3207 (982, 7080) (P = 0.19, Cohen's d = 0.16); and day 28: 1377 (697, 2248) compared with 1779 (660, 3977) (P = 0.27, Cohen's d = 0.19), respectively. When comparing measured sIgA concentrations between days 0 and 5, we found no treatment allocation effects [β: -0.24 (-0.65, 0.18); P = 0.26] or interaction between treatment and specimen collection day [β: -0.003 (-0.09, 0.09); P = 0.95]. Although stool sIgA decreased between day 5 and day 28 within both groups (P < 0.001), there were no differences between the probiotic and placebo groups in the median changes in sIgA concentrations when comparing day 0 to day 5 median (IQR) [500 (-1135, 2362) compared with 362 (-1122, 4256); P = 0.77, Cohen's d = 0.075] and day 5 to day 28 [-1035 (-3130, 499) compared with -1260 (-4437, 843); P = 0.70, Cohen's d = 0.067], respectively.
Conclusions:
We found no effect of an L. rhamnosus/helveticus probiotic, relative to placebo, on stool IgA concentrations. This trial was registered at clinicaltrials.gov as NCT01853124.
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