Gut microbiota and fecal metabolites in sustained unresponsiveness by oral immunotherapy in school-age children with cow's milk allergy

Allergol Int. 2024 Jan;73(1):126-136. doi: 10.1016/j.alit.2023.10.001. Epub 2023 Nov 1.

Abstract

Background: Oral immunotherapy (OIT) can ameliorate cow's milk allergy (CMA); however, the achievement of sustained unresponsiveness (SU) is challenging. Regarding the pathogenesis of CMA, recent studies have shown the importance of gut microbiota (Mb) and fecal water-soluble metabolites (WSMs), which prompted us to determine the change in clinical and gut environmental factors important for acquiring SU after OIT for CMA.

Methods: We conducted an ancillary cohort study of a multicenter randomized, parallel-group, delayed-start design study on 32 school-age children with IgE-mediated CMA who underwent OIT for 13 months. We defined SU as the ability to consume cow's milk exceeding the target dose in a double-blind placebo-controlled food challenge after OIT followed by a 2-week-avoidance. We longitudinally collected 175 fecal specimens and clustered the microbiome and metabolome data into 29 Mb- and 12 WSM-modules.

Results: During OIT, immunological factors improved in all participants. However, of the 32 participants, 4 withdrew because of adverse events, and only 7 were judged SU. Gut environmental factors shifted during OIT, but only in the beginning, and returned to the baseline at the end. Of these factors, milk- and casein-specific IgE and the Bifidobacterium-dominant module were associated with SU (milk- and casein-specific IgE; OR for 10 kUA/L increments, 0.67 and 0.66; 95%CI, 0.41-0.93 and 0.42-0.90; Bifidobacterium-dominant module; OR for 0.01 increments, 1.40; 95%CI, 1.10-2.03), and these associations were observed until the end of OIT.

Conclusions: In this study, we identified the clinical and gut environmental factors associated with SU acquisition in CM-OIT.

Keywords: Casein-specific IgE; Cow's milk allergy; Fecal metabolites; Gut microbiota; Oral immunotherapy.

Publication types

  • Randomized Controlled Trial
  • Multicenter Study

MeSH terms

  • Animals
  • Caseins
  • Cattle
  • Child
  • Cohort Studies
  • Female
  • Gastrointestinal Microbiome*
  • Humans
  • Immunoglobulin E
  • Immunotherapy
  • Infant
  • Milk
  • Milk Hypersensitivity* / therapy

Substances

  • Caseins
  • Immunoglobulin E