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IDO in the Tumor Microenvironment: Inflammation, Counter-Regulation, and Tolerance.
Munn, David H; Mellor, Andrew L.
Affiliation
  • Munn DH; Cancer Center and Department of Pediatrics, Medical College of Georgia, Georgia Regents University, Augusta, GA 30904, USA. Electronic address: dmunn@gru.edu.
  • Mellor AL; Institute of Cellular Medicine, Medical School, Newcastle University, Framlington Place, Newcastle-upon-Tyne, NE2 4HH, UK. Electronic address: andrew.mellor@ncl.ac.uk.
Trends Immunol ; 37(3): 193-207, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26839260
Indoleamine 2,3-dioxygenase (IDO) has immunoregulatory roles associated with tryptophan metabolism. These include counter-regulation (controlling inflammation) and acquired tolerance in T cells. Recent findings reveal that IDO can be triggered by innate responses during tumorigenesis, and also by attempted T cell activation, either spontaneous or due to immunotherapy. Here we review the current understanding of mechanisms by which IDO participates in the control of inflammation and in peripheral tolerance. Focusing on the tumor microenvironment, we examine the role of IDO in response to apoptotic cells and the impact of IDO on Treg cell function. We discuss how the counter-regulatory and tolerogenic functions of IDO can be targeted for cancer immunotherapy and present an overview of the current clinical progress in this area.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Immunosuppression Therapy / T-Lymphocytes, Regulatory / Indoleamine-Pyrrole 2,3,-Dioxygenase / Immune Tolerance / Immunotherapy / Inflammation / Neoplasms Limits: Animals / Humans Language: En Journal: Trends Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Immunosuppression Therapy / T-Lymphocytes, Regulatory / Indoleamine-Pyrrole 2,3,-Dioxygenase / Immune Tolerance / Immunotherapy / Inflammation / Neoplasms Limits: Animals / Humans Language: En Journal: Trends Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2016 Type: Article