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Immunological relevance of the coevolution of IDO1 and AHR

Journal

FRONTIERS IN IMMUNOLOGY
Volume 5, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2014.00521

Keywords

aryl hydrocarbon receptor; 2,3-dioxygenase; tryptophan-2,3-dioxygenase

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Funding

  1. National Multiple Sclerosis Society
  2. National Institutes of Health
  3. Sigrid Juselius Foundation
  4. Paulo Foundation
  5. Finnish Multiple Sclerosis Foundation

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The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor initially identified because of its role in controlling the cellular response to environmental molecules. More recently, AHR has been shown to play a crucial role in controlling innate and adaptive immune responses through several mechanisms, one of which is the regulation of tryptophan metabolism. Indoleamine-2,3-dioxygenase (IDO) and tryptophan-2,3-dioxygenase (TDO) are considered rate-limiting enzymes in the tryptophan catabolism and play important roles in the regulation of the immunity. Moreover, AHR and IDO/TDO are closely interconnected: AHR regulates IDO and TDO expression, and kynurenine produced by IDO/TDO is an AHR agonist. In this review, we propose to examine the relationship between AHR and IDO/TDO and its relevance for the regulation of the immune response in health and disease.

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