Chronic inflammation that facilitates tumor progression creates local immune suppression by inducing indoleamine 2,3 dioxygenase

• Published in: Proceedings of the National Academy of Sciences - PNAS 2008-11, Vol.105 (44), p.17073-17078
• Main Authors: Muller, Alexander J, Sharma, Madhav D, Chandler, Phillip R, DuHadaway, James B, Everhart, Mary E, Johnson, Burles A. III, Kahler, David J, Pihkala, Jeanene, Soler, Alejandro Peralta, Munn, David H, Prendergast, George C, Mellor, Andrew L
• Format: Article
• Language: English
• Subjects: Animals; Biological Sciences; Cancer; Cells; Cultured cells; Dendritic cells; Dendritic Cells - cytology; Dendritic Cells - enzymology; Dendritic Cells - immunology; Dermatitis, Contact - enzymology; Dermatitis, Contact - immunology; Dermatitis, Contact - pathology; Disease Progression; Gene expression; Immune Tolerance - immunology; Indoleamine-Pyrrole 2,3,-Dioxygenase - genetics; Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism; Inflammation; Lesions; Lymph Nodes - enzymology; Lymph Nodes - immunology; Lymph Nodes - pathology; Lymphatic system; Mice; Mice, Inbred C57BL; Models, Animal; Noise reduction; Papilloma; Papilloma - immunology; Papilloma - pathology; Proteins; Rodents; Signal transduction; Signal Transduction - immunology; Skin Neoplasms - immunology; Skin Neoplasms - pathology; T lymphocytes; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; Tetradecanoylphorbol Acetate - pharmacology; Tumors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.0806173105

Topical application of phorbol myristate acetate (PMA) elicits intense local inflammation that facilitates outgrowth of premalignant lesions in skin after carcinogen exposure. The inflammatory response to PMA treatment activates immune stimulatory mechanisms. However, we show here that PMA exposure also induces plasmacytoid dendritic cells (pDCs) in local draining lymph nodes (dLNs) to express indoleamine 2,3 dioxygenase (IDO), which confers T cell suppressor activity on pDCs. The induced IDO-mediated inhibitory activity in this subset of pDCs was potent, dominantly suppressing the T cell stimulatory activity of other DCs that comprise the major fraction of dLN DCs. IDO induction in pDCs depended on inflammatory signaling by means of IFN type I and II receptors, the TLR/IL-1 signaling adaptor MyD88, and on cellular stress responses to amino acid withdrawal by means of the integrated stress response kinase GCN2. Consistent with the hypothesis that T cell suppressive, IDO⁺ pDCs elicited by PMA exposure create local immune privilege that favors tumor development, IDO-deficient mice exhibited a robust tumor-resistant phenotype in the standard DMBA/PMA 2-stage carcinogenesis model of skin papilloma formation. Thus, IDO is a key immunosuppressive factor that facilitates tumor progression in this setting of chronic inflammation driven by repeated topical PMA exposure.