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Author Notes:

Edmund K. Waller MD, PhD, FACP, Professor of Medicine and Oncology, Winship Cancer Institute Emory University, Atlanta, Georgia 30322; Phone 404-727-4995; Fax 404-778-5530. Email: ewaller@emory.edu

These authors contributed equally: Muna Qayed, David Michonneau These authors jointly supervised this work: Gérard Socié, Edmund K. Waller

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Subject:

Research Funding:

National Institutes of Health, Bethesda, MD (1R01CA188523-01A1).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • ARYL-HYDROCARBON RECEPTOR
  • INTESTINAL MICROBIOTA
  • STEM-CELL
  • T-CELLS
  • TRYPTOPHAN-METABOLISM
  • GUT MICROBIOME
  • IMMUNITY
  • AHR
  • 2,3-DIOXYGENASE
  • TRANSPLANTATION

Indole derivatives, microbiome and graft versus host disease

Tools:

Journal Title:

CURRENT OPINION IN IMMUNOLOGY

Volume:

Volume 70

Publisher:

, Pages 40-47

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Graft versus host disease is a life-threatening complication following allogeneic hematopoietic stem cell transplantation driven by donor T cells reacting against disparate host antigens. Immune homeostasis within the gut plays a major role in the graft versus host response. Gut microbiota and its metabolites impact gut integrity, inflammation and immune activation within the gut. This review will focus on the role of indoles, a product of microbiota metabolism, on gut homeostasis and our current understanding on how that modulates graft versus host disease.

Copyright information:

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/rdf).
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