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Indoleamine 2,3-dioxygenase (IDO): Biology and Target in Cancer Immunotherapies
被引:66
作者:
Selvan, Senthamil R.
[1
]
Dowling, John P.
[2
]
Kelly, William K.
[1
]
Lin, Jianqing
[1
]
机构:
[1] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Med Oncol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Immunol & Microbial Pathogenesis Grad Program, Philadelphia, PA 19107 USA
关键词:
Cancer immunotherapy;
combination therapy;
indoleamine 2,3-dioxygenase (IDO);
IDO inhibitors;
immune tolerance;
REGULATORY T-CELLS;
NATURAL-KILLER-CELLS;
PLASMACYTOID DENDRITIC CELLS;
TUMOR-INFILTRATING LYMPHOCYTES;
BLOOD MONONUCLEAR-CELLS;
DRAINING LYMPH-NODES;
SUPPRESSOR-CELLS;
PERIPHERAL-BLOOD;
LUNG-CANCER;
TRYPTOPHAN CATABOLISM;
D O I:
10.2174/1568009615666151030102250
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Indoleamine 2,3-dioxygenase (IDO) is a heme-containing oxidoreductase that catalyzes the initial and rate-limiting step in the breakdown of non-dietary tryptophan. The biology and immunomodulatory role for IDO is discussed in this review with a focus on its interaction with immune cells and its potential therapeutic target in the clinic. IDO has been revealed to be a central regulator of immune responses in a broad variety of physiological and pathological settings, mostly serving as a multifaceted negative feedback mechanism, to self-regulate immune responses. IDO is considered a therapeutic target in cancer and the use of IDO inhibitors as single agent or in combination with other treatment modalities are under active investigation.
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页码:755 / 764
页数:10
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