Literature DB >> 17476344

Indoleamine 2,3-dioxygenase and tumor-induced tolerance.

David H Munn1, Andrew L Mellor.   

Abstract

Tumors arise from normal cells of the body through genetic mutation. Although such genetic mutation often leads to the expression of abnormal antigens, the immune system fails to respond effectively to these antigens; that is, it is tolerant of these antigens. This acquired state of tolerance must be overcome for cancer immunotherapy to succeed. Indoleamine 2,3-dioxygenase (IDO) is one molecular mechanism that contributes to tumor-induced tolerance. IDO helps create a tolerogenic milieu in the tumor and the tumor-draining lymph nodes, both by direct suppression of T cells and enhancement of local Treg-mediated immunosuppression. It can also function as an antagonist to other activators of antitumor immunity. Therefore, strategies to block IDO might enhance the effectiveness of tumor immunotherapy.

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Year:  2007        PMID: 17476344      PMCID: PMC1857253          DOI: 10.1172/JCI31178

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  123 in total

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Journal:  J Clin Invest       Date:  2006-11-16       Impact factor: 14.808

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7.  Modulation of tryptophan catabolism by human leukemic cells results in the conversion of CD25- into CD25+ T regulatory cells.

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9.  Indoleamine 2,3-dioxygenase is a novel prognostic indicator for endometrial cancer.

Authors:  K Ino; N Yoshida; H Kajiyama; K Shibata; E Yamamoto; K Kidokoro; N Takahashi; M Terauchi; A Nawa; S Nomura; T Nagasaka; O Takikawa; F Kikkawa
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  402 in total

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Journal:  Haematologica       Date:  2014-11-14       Impact factor: 9.941

Review 2.  Indoleamine 2,3-dioxygenase as a modifier of pathogenic inflammation in cancer and other inflammation-associated diseases.

Authors:  G C Prendergast; M Y Chang; L Mandik-Nayak; R Metz; A J Muller
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Review 3.  Pancreatic ductal adenocarcinoma: a review of immunologic aspects.

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Review 4.  Evaluation of current cancer immunotherapy: hemato-oncology.

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6.  Strategic Incorporation of Polarity in Heme-Displacing Inhibitors of Indoleamine-2,3-dioxygenase-1 (IDO1).

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7.  Induction of IDO by bacille Calmette-Guérin is responsible for development of murine depressive-like behavior.

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Journal:  J Immunol       Date:  2009-03-01       Impact factor: 5.422

8.  Plasmacytoid dendritic cells from mouse tumor-draining lymph nodes directly activate mature Tregs via indoleamine 2,3-dioxygenase.

Authors:  Madhav D Sharma; Babak Baban; Phillip Chandler; De-Yan Hou; Nagendra Singh; Hideo Yagita; Miyuki Azuma; Bruce R Blazar; Andrew L Mellor; David H Munn
Journal:  J Clin Invest       Date:  2007-09       Impact factor: 14.808

9.  LW106, a novel indoleamine 2,3-dioxygenase 1 inhibitor, suppresses tumour progression by limiting stroma-immune crosstalk and cancer stem cell enrichment in tumour micro-environment.

Authors:  Rong Fu; Yi-Wei Zhang; Hong-Mei Li; Wen-Cong Lv; Li Zhao; Qing-Long Guo; Tao Lu; Stephen J Weiss; Zhi-Yu Li; Zhao-Qiu Wu
Journal:  Br J Pharmacol       Date:  2018-06-03       Impact factor: 8.739

10.  The role of plasma IDO activity as a diagnostic marker of patients with colorectal cancer.

Authors:  M Cavia-Saiz; P Muñiz Rodríguez; B Llorente Ayala; M García-González; M J Coma-Del Corral; C García Girón
Journal:  Mol Biol Rep       Date:  2014-01-17       Impact factor: 2.316

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