Targeting the gut microbiome: An emerging trend in hematopoietic stem cell transplantation.
Biodiversity
Combined Modality Therapy
Fecal Microbiota Transplantation
Gastrointestinal Microbiome
/ drug effects
Graft vs Host Disease
/ etiology
Hematologic Neoplasms
/ complications
Hematopoietic Stem Cell Transplantation
/ adverse effects
Humans
Prognosis
Transplantation Conditioning
/ adverse effects
Transplantation, Homologous
Treatment Outcome
Bacterial diversity
Cancer treatment
Fecal microbiota transplantation
Graft-versus-host disease
Hematopoietic stem cell transplantation
Microbiome
Probiotics
Journal
Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558
Informations de publication
Date de publication:
07 2021
07 2021
Historique:
received:
23
06
2020
revised:
09
10
2020
accepted:
02
12
2020
pubmed:
13
2
2021
medline:
4
9
2021
entrez:
12
2
2021
Statut:
ppublish
Résumé
Mounting evidence has demonstrated the critical role of the gut microbiome in different cancer treatment modalities showing intensive crosstalk between microbiota and the host immune system. In cancer patients receiving hematopoietic stem cell transplantation (HSCT), conditioning regimens including chemotherapy, radiotherapy, and immunosuppressive therapy, as well as antimicrobial prophylaxis, result in intestinal barrier disruption and massive changes in microbiota composition. According to clinical studies, a drastic loss of microbial diversity during HSCT is associated with enhanced pro-inflammatory immune response and an increased risk of transplant-related complications such as graft-versus-host disease (GvHD) and mortality. In this review, we outline the current understanding of the role of microbiota diversity in the patient response to cancer therapies and highlight the impact of changes in the gut microbiome on clinical outcomes in post-HSCT patients. Moreover, the therapeutic implications of microbiota modulation by probiotics, prebiotics, and fecal microbiota transplantation (FMT) in hematologic cancer patients receiving HSCT are discussed.
Identifiants
pubmed: 33573867
pii: S0268-960X(20)30140-5
doi: 10.1016/j.blre.2020.100790
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
100790Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.