Prebiotics protect against acute graft-versus-host disease and preserve the gut microbiota in stem cell transplantation

Author:

Yoshifuji Kota12,Inamoto Kyoko1,Kiridoshi Yuko3,Takeshita Kozue4,Sasajima Satoshi4,Shiraishi Yukiko5,Yamashita Yuko6,Nisaka Yuko6,Ogura Yukari5,Takeuchi Rie5,Toya Takashi1ORCID,Igarashi Aiko1,Najima Yuho1,Doki Noriko1,Kobayashi Takeshi1,Ohashi Kazuteru1,Suda Wataru7ORCID,Atarashi Koji34ORCID,Shiota Atsushi34,Hattori Masahira78,Honda Kenya3479,Kakihana Kazuhiko1ORCID

Affiliation:

1. Hematology Division, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan;

2. Department of Hematology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan;

3. JSR-Keio University Medical and Chemical Innovation Center (JKiC), Tokyo, Japan,

4. Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan;

5. Nutrition Division and

6. Nursing Division, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan;

7. RIKEN Center for Integrative Medical Sciences (IMS), Yokohama City, Japan;

8. Graduate School of Advanced Science and Engineering, Waseda University, Tokyo, Japan; and

9. AMED-LEAP, Japan Agency for Medical Research and Development, Tokyo, Japan

Abstract

Abstract Acute graft-versus-host disease (aGVHD) is a major cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Therefore, management of aGVHD is important for successful transplantation. Mucosal damage and alteration of the gut microbiota after allo-HSCT are key factors in the development of aGVHD. We conducted a prospective study to evaluate the ability of prebiotics, which can alleviate mucosal damage and manipulate the gut microbiota, to mitigate posttransplantation complications, including aGVHD. Resistant starch (RS) and a commercially available prebiotics mixture, GFO, were administered to allo-HSCT recipients from pretransplantation conditioning to day 28 after allo-HSCT. Prebiotic intake mitigated mucosal injury and reduced the incidence of all aGVHD grades combined and of aGVHD grades 2 to 4. The cumulative incidence of skin aGVHD was markedly decreased by prebiotics intake. Furthermore, the gut microbial diversity was well maintained and butyrate-producing bacterial population were preserved by prebiotics intake. In addition, the posttransplantation fecal butyrate concentration was maintained or increased more frequently in the prebiotics group. These observations indicate that prebiotic intake may be an effective strategy for preventing aGVHD in allo-HSCT, thereby improving treatment outcomes and the clinical utility of stem cell transplantation approaches. This study was registered on the University Hospital Medical Information Network (UMIN) clinical trials registry (https://www.umin.ac.jp/ctr/index.htm) as #UMIN000027563.

Publisher

American Society of Hematology

Subject

Hematology

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