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A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD

Graft-versus-host disease (GVHD) is a pathological process caused by an exaggerated donor lymphocyte response to host antigens after allogeneic hematopoietic cell transplantation (allo-HCT). Donor T cells undergo extensive clonal expansion and differentiation, which culminate in damage to recipient...

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Autores principales: Sofi, M. Hanief, Wu, Yongxia, Ticer, Taylor, Schutt, Steven, Bastian, David, Choi, Hee-Jin, Tian, Linlu, Mealer, Corey, Liu, Chen, Westwater, Caroline, Armeson, Kent E., Alekseyenko, Alexander V., Yu, Xue-Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934839/
https://www.ncbi.nlm.nih.gov/pubmed/33554953
http://dx.doi.org/10.1172/jci.insight.136841
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author Sofi, M. Hanief
Wu, Yongxia
Ticer, Taylor
Schutt, Steven
Bastian, David
Choi, Hee-Jin
Tian, Linlu
Mealer, Corey
Liu, Chen
Westwater, Caroline
Armeson, Kent E.
Alekseyenko, Alexander V.
Yu, Xue-Zhong
author_facet Sofi, M. Hanief
Wu, Yongxia
Ticer, Taylor
Schutt, Steven
Bastian, David
Choi, Hee-Jin
Tian, Linlu
Mealer, Corey
Liu, Chen
Westwater, Caroline
Armeson, Kent E.
Alekseyenko, Alexander V.
Yu, Xue-Zhong
author_sort Sofi, M. Hanief
collection PubMed
description Graft-versus-host disease (GVHD) is a pathological process caused by an exaggerated donor lymphocyte response to host antigens after allogeneic hematopoietic cell transplantation (allo-HCT). Donor T cells undergo extensive clonal expansion and differentiation, which culminate in damage to recipient target organs. Damage to the gastrointestinal tract is a main contributor to morbidity and mortality. The loss of diversity among intestinal bacteria caused by pretransplant conditioning regimens leads to an outgrowth of opportunistic pathogens and exacerbated GVHD after allo-HCT. Using murine models of allo-HCT, we found that an increase of Bacteroides in the intestinal microbiota of the recipients was associated with reduced GVHD in mice given fecal microbial transplantation. Administration of Bacteroides fragilis through oral gavage increased gut microbiota diversity and beneficial commensal bacteria and significantly ameliorated acute and chronic GVHD development. Preservation of gut integrity following B. fragilis exposure was likely attributed to increased short chain fatty acids, IL-22, and regulatory T cells, which in turn improved gut tight junction integrity and reduced inflammatory cytokine production of pathogenic T cells. The current study provides a proof of concept that a single strain of commensal bacteria can be a safe and effective means to protect gut integrity and ameliorate GVHD after allo-HCT.
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spelling pubmed-79348392021-03-09 A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD Sofi, M. Hanief Wu, Yongxia Ticer, Taylor Schutt, Steven Bastian, David Choi, Hee-Jin Tian, Linlu Mealer, Corey Liu, Chen Westwater, Caroline Armeson, Kent E. Alekseyenko, Alexander V. Yu, Xue-Zhong JCI Insight Research Article Graft-versus-host disease (GVHD) is a pathological process caused by an exaggerated donor lymphocyte response to host antigens after allogeneic hematopoietic cell transplantation (allo-HCT). Donor T cells undergo extensive clonal expansion and differentiation, which culminate in damage to recipient target organs. Damage to the gastrointestinal tract is a main contributor to morbidity and mortality. The loss of diversity among intestinal bacteria caused by pretransplant conditioning regimens leads to an outgrowth of opportunistic pathogens and exacerbated GVHD after allo-HCT. Using murine models of allo-HCT, we found that an increase of Bacteroides in the intestinal microbiota of the recipients was associated with reduced GVHD in mice given fecal microbial transplantation. Administration of Bacteroides fragilis through oral gavage increased gut microbiota diversity and beneficial commensal bacteria and significantly ameliorated acute and chronic GVHD development. Preservation of gut integrity following B. fragilis exposure was likely attributed to increased short chain fatty acids, IL-22, and regulatory T cells, which in turn improved gut tight junction integrity and reduced inflammatory cytokine production of pathogenic T cells. The current study provides a proof of concept that a single strain of commensal bacteria can be a safe and effective means to protect gut integrity and ameliorate GVHD after allo-HCT. American Society for Clinical Investigation 2021-02-08 /pmc/articles/PMC7934839/ /pubmed/33554953 http://dx.doi.org/10.1172/jci.insight.136841 Text en © 2021 Sofi et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Sofi, M. Hanief
Wu, Yongxia
Ticer, Taylor
Schutt, Steven
Bastian, David
Choi, Hee-Jin
Tian, Linlu
Mealer, Corey
Liu, Chen
Westwater, Caroline
Armeson, Kent E.
Alekseyenko, Alexander V.
Yu, Xue-Zhong
A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title_full A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title_fullStr A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title_full_unstemmed A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title_short A single strain of Bacteroides fragilis protects gut integrity and reduces GVHD
title_sort single strain of bacteroides fragilis protects gut integrity and reduces gvhd
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934839/
https://www.ncbi.nlm.nih.gov/pubmed/33554953
http://dx.doi.org/10.1172/jci.insight.136841
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