Your browser doesn't support javascript.
loading
Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency.
Ono, Shintaro; Takeshita, Kozue; Kiridoshi, Yuko; Kato, Motohiro; Kamiya, Takahiro; Hoshino, Akihiro; Yanagimachi, Masakatsu; Arai, Katsuhiro; Takeuchi, Ichiro; Toita, Nariaki; Imamura, Toshihiko; Sasahara, Yoji; Sugita, Junichi; Hamamoto, Kazuko; Takeuchi, Masanobu; Saito, Shoji; Onuma, Masaei; Tsujimoto, Hiroshi; Yasui, Masahiro; Taga, Takashi; Arakawa, Yuki; Mitani, Yuichi; Yamamoto, Nobuyuki; Imai, Kohsuke; Suda, Wataru; Hattori, Masahira; Ohara, Osamu; Morio, Tomohiro; Honda, Kenya; Kanegane, Hirokazu.
Affiliation
  • Ono S; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan; Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Japan.
  • Takeshita K; Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan; JSR-Keio University Medical and Chemical Innovation Center (JKiC), Tokyo, Japan.
  • Kiridoshi Y; JSR-Keio University Medical and Chemical Innovation Center (JKiC), Tokyo, Japan.
  • Kato M; Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
  • Kamiya T; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Hoshino A; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Yanagimachi M; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan; Department of Hematology and Oncology, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Arai K; Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.
  • Takeuchi I; Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.
  • Toita N; Department of Pediatrics, Sapporo Kosei General Hospital, Sapporo, Japan.
  • Imamura T; Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
  • Sasahara Y; Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Sugita J; Department of Hematology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
  • Hamamoto K; Department of Pediatrics, Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
  • Takeuchi M; Department of Pediatrics, Yokohama City University Hospital, Yokohama, Japan.
  • Saito S; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Onuma M; Department of Hematology and Oncology, Miyagi Children's Hospital, Sendai, Japan.
  • Tsujimoto H; Department of Pediatrics, Wakayama Medical University, Wakayama, Japan.
  • Yasui M; Department of Hematology/Oncology, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Taga T; Department of Pediatrics, Shiga University of Medical Science, Otsu, Japan.
  • Arakawa Y; Department of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
  • Mitani Y; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Yamamoto N; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Imai K; Department of Community Pediatrics, Perinatal and Maternal Medicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Suda W; RIKEN Center for Integrative Medical Sciences (IMS), Yokohama City, Japan.
  • Hattori M; RIKEN Center for Integrative Medical Sciences (IMS), Yokohama City, Japan; Graduate School of Advanced Science and Engineering, Waseda University, Tokyo, Japan.
  • Ohara O; Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Japan; Department of Technology Development, Kazusa DNA Research Institute, Chiba, Japan.
  • Morio T; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Honda K; Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan; JSR-Keio University Medical and Chemical Innovation Center (JKiC), Tokyo, Japan; RIKEN Center for Integrative Medical Sciences (IMS), Yokohama City, Japan.
  • Kanegane H; Department of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan. Electronic address: hkanegane.ped@tmd.ac.jp.
J Allergy Clin Immunol Pract ; 9(10): 3767-3780, 2021 10.
Article in En | MEDLINE | ID: mdl-34246792
ABSTRACT

BACKGROUND:

X-linked inhibitor of apoptosis protein (XIAP) deficiency is an infrequent inborn error of immunity that is often associated with refractory inflammatory bowel disease (IBD). The natural course of XIAP deficiency is typically associated with poor prognosis, and hematopoietic cell transplantation (HCT) is the only curative treatment.

OBJECTIVE:

To study (1) the effect of HCT on patients with XIAP deficiency undergoing HCT, (2) the status of XIAP deficiency-associated IBD after HCT, and (3) the gut microbiota of XIAP deficiency-associated IBD before and after HCT.

METHODS:

A nationwide survey of patients with XIAP deficiency was conducted. A spreadsheet questionnaire was collected from the physicians. Feces samples collected from the patients before and after HCT and their healthy family members were analyzed.

RESULTS:

Twenty-six patients with XIAP deficiency underwent HCT by the end of March 2020, and 22 patients (84.6%) survived. All the survivors underwent a fludarabine-based reduced-intensity condition regimen. Acute graft-versus-host disease was observed in 17 patients (65.4%). Nineteen patients experienced refractory IBD before undergoing HCT. IBD improved remarkably after HCT. After HCT, the colonoscopic and pathological symptoms were restored to normal, and the pediatric ulcerative colitis activity index improved significantly. Gut microbiota indicated dysbiosis before HCT; however, it was improved to resemble that of the healthy family members after HCT.

CONCLUSIONS:

This study revealed that HCT has a favorable outcome for XIAP deficiency. HCT rescues gut inflammation and dysbiosis in patients with XIAP deficiency.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / Hematopoietic Stem Cell Transplantation / Gastrointestinal Microbiome Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Allergy Clin Immunol Pract Year: 2021 Document type: Article Affiliation country: Japan Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / Hematopoietic Stem Cell Transplantation / Gastrointestinal Microbiome Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Allergy Clin Immunol Pract Year: 2021 Document type: Article Affiliation country: Japan Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA