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

  • Shibata Ryohei
    Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences Immunobiology Laboratory, Graduate School of Medical Life Science, Yokohama City University Department of Pediatric Surgery, Graduate School of Medicine, Chiba University
  • Itoh Naoka
    Department of Pediatrics, National Hospital Organization Kanagawa National Hospital
  • Nakanishi Yumiko
    Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences Immunobiology Laboratory, Graduate School of Medical Life Science, Yokohama City University
  • Kato Tamotsu
    Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences Immunobiology Laboratory, Graduate School of Medical Life Science, Yokohama City University
  • Suda Wataru
    Laboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences
  • Nagao Mizuho
    Allergy Center, National Hospital Organization Mie National Hospital
  • Iwata Tsutomu
    The Graduate School of Tokyo Kasei University
  • Yoshida Hideo
    Department of Pediatric Surgery, Graduate School of Medicine, Chiba University
  • Hattori Masahira
    Laboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences Graduate School of Advanced Science and Engineering, Waseda University
  • Fujisawa Takao
    Allergy Center, National Hospital Organization Mie National Hospital
  • Shimojo Naoki
    Center for Preventive Medical Sciences, Chiba University
  • Ohno Hiroshi
    Laboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences Immunobiology Laboratory, Graduate School of Medical Life Science, Yokohama City University Laboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences

抄録

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

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