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Applications of gut microbiota in patients with hematopoietic stem-cell transplantation

Studies of the gut microbiota (GM) have demonstrated the close link between human wellness and intestinal commensal bacteria, which mediate development of the host immune system. The dysbiosis, a disruption of the microbiome natural balance, can cause serious health problems. Patients undergoing all...

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Autores principales: Yu, Jifeng, Sun, Hao, Cao, Weijie, Han, Lijie, Song, Yongping, Wan, Dingming, Jiang, Zhongxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716583/
https://www.ncbi.nlm.nih.gov/pubmed/33292670
http://dx.doi.org/10.1186/s40164-020-00194-y
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author Yu, Jifeng
Sun, Hao
Cao, Weijie
Han, Lijie
Song, Yongping
Wan, Dingming
Jiang, Zhongxing
author_facet Yu, Jifeng
Sun, Hao
Cao, Weijie
Han, Lijie
Song, Yongping
Wan, Dingming
Jiang, Zhongxing
author_sort Yu, Jifeng
collection PubMed
description Studies of the gut microbiota (GM) have demonstrated the close link between human wellness and intestinal commensal bacteria, which mediate development of the host immune system. The dysbiosis, a disruption of the microbiome natural balance, can cause serious health problems. Patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) may cause significant changes in GM due to their underlying malignancies and exposure to extensive chemotherapy and systemic antibiotics, which may lead to different disorders. There are complex and multi-directional interactions among intestinal inflammation, GM and immune reactivity after HSCT. There is considerable effect of the human intestinal microbiome on clinical course following HSCT. Some bacteria in the intestinal ecosystem may be potential biomarkers or therapeutic targets for preventing relapse and improving survival rate after HSCT. Microbiota can be used as predictor of mortality in allo-HSCT. Two different strategies with targeted modulation of GM, preemptive and therapeutic, have been used for preventing or treating GM dysbiosis in patients with HSCT. Preemptive strategies include enteral nutrition (EN), prebiotic, probiotic, fecal microbiota transplantation (FMT) and antibiotic strategies, while therapeutic strategies include FMT, probiotic and lactoferrine usages. In this review, we summarize the advance of therapies targeting GM in patients with HSCT.
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spelling pubmed-77165832020-12-04 Applications of gut microbiota in patients with hematopoietic stem-cell transplantation Yu, Jifeng Sun, Hao Cao, Weijie Han, Lijie Song, Yongping Wan, Dingming Jiang, Zhongxing Exp Hematol Oncol Review Studies of the gut microbiota (GM) have demonstrated the close link between human wellness and intestinal commensal bacteria, which mediate development of the host immune system. The dysbiosis, a disruption of the microbiome natural balance, can cause serious health problems. Patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) may cause significant changes in GM due to their underlying malignancies and exposure to extensive chemotherapy and systemic antibiotics, which may lead to different disorders. There are complex and multi-directional interactions among intestinal inflammation, GM and immune reactivity after HSCT. There is considerable effect of the human intestinal microbiome on clinical course following HSCT. Some bacteria in the intestinal ecosystem may be potential biomarkers or therapeutic targets for preventing relapse and improving survival rate after HSCT. Microbiota can be used as predictor of mortality in allo-HSCT. Two different strategies with targeted modulation of GM, preemptive and therapeutic, have been used for preventing or treating GM dysbiosis in patients with HSCT. Preemptive strategies include enteral nutrition (EN), prebiotic, probiotic, fecal microbiota transplantation (FMT) and antibiotic strategies, while therapeutic strategies include FMT, probiotic and lactoferrine usages. In this review, we summarize the advance of therapies targeting GM in patients with HSCT. BioMed Central 2020-12-04 /pmc/articles/PMC7716583/ /pubmed/33292670 http://dx.doi.org/10.1186/s40164-020-00194-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Yu, Jifeng
Sun, Hao
Cao, Weijie
Han, Lijie
Song, Yongping
Wan, Dingming
Jiang, Zhongxing
Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title_full Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title_fullStr Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title_full_unstemmed Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title_short Applications of gut microbiota in patients with hematopoietic stem-cell transplantation
title_sort applications of gut microbiota in patients with hematopoietic stem-cell transplantation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716583/
https://www.ncbi.nlm.nih.gov/pubmed/33292670
http://dx.doi.org/10.1186/s40164-020-00194-y
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