Host Indoleamine 2,3-Dioxygenase: Contribution to Systemic Acquired Tumor Tolerance

被引:71
|
作者
Johnson, Theodore S. [1 ,2 ,3 ]
Munn, David H. [1 ,2 ,3 ]
机构
[1] Georgia Hlth Sci Univ, Dept Pediat, Augusta, GA 30912 USA
[2] Georgia Hlth Sci Univ, Immunotherapy Ctr, Augusta, GA 30912 USA
[3] Georgia Hlth Sci Univ, GHSU Canc Ctr, Augusta, GA 30912 USA
关键词
Indoleamine 2,3-dioxygenase; tumor; tolerance; IDO; indoleamine; dioxygenase; host; Treg; REGULATORY T-CELLS; ARYL-HYDROCARBON RECEPTOR; PLASMACYTOID DENDRITIC CELLS; ANTIGEN-PRESENTING CELLS; MYELOID-LEUKEMIA CELLS; TRYPTOPHAN CATABOLISM; INTERFERON-GAMMA; IFN-GAMMA; CUTTING EDGE; IDO ACTIVITY;
D O I
10.3109/08820139.2012.689405
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Indoleamine 2,3-dioxygenase (IDO) is a natural mechanism of creating acquired tolerance in a variety of physiological settings. This endogenous tolerogenic pathway has important functions in regulating the magnitude of immune responses in settings of infection, pregnancy, tissue transplantation, mucosal interfaces and others. Whether for angiogenesis, stromal formation or immunologic tolerance, tumors often rely on recruiting host mechanisms. IDO is one such potent endogenous mechanism that appears to be frequently hijacked by tumors to establish systemic immune tolerance to tumor antigens. IDO can be expressed by tumors themselves, but, in addition, its natural site of expression is the host immune cells recruited by the tumor (particularly dendritic cells and macrophages). Therapeutic strategies that target the IDO pathway have been shown to synergize with standard chemotherapy and experimental immunotherapies to break tumor-induced tolerance. When such strategies target IDO expressed in host cells, they may be able to disrupt tolerance without creating intrinsic tumor cell drug resistance.
引用
收藏
页码:765 / 797
页数:33
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