| Literature DB >> 32991720 |
Kota Yoshifuji1,2, Kyoko Inamoto1, Yuko Kiridoshi3, Kozue Takeshita4, Satoshi Sasajima4, Yukiko Shiraishi5, Yuko Yamashita6, Yuko Nisaka6, Yukari Ogura5, Rie Takeuchi5, Takashi Toya1, Aiko Igarashi1, Yuho Najima1, Noriko Doki1, Takeshi Kobayashi1, Kazuteru Ohashi1, Wataru Suda7, Koji Atarashi3,4, Atsushi Shiota3,4, Masahira Hattori7,8, Kenya Honda3,4,7,9, Kazuhiko Kakihana1.
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.Entities:
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Year: 2020 PMID: 32991720 PMCID: PMC7556149 DOI: 10.1182/bloodadvances.2020002604
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529