王婷, 文辉, 崔华清, 尹大力. 吲哚胺2,3-双加氧酶1(IDO1)抑制剂的研究进展J. 药学学报, 2021,56(3): 723-733. doi: 10.16438/j.0513-4870.2020-1421
引用本文: 王婷, 文辉, 崔华清, 尹大力. 吲哚胺2,3-双加氧酶1(IDO1)抑制剂的研究进展J. 药学学报, 2021,56(3): 723-733. doi: 10.16438/j.0513-4870.2020-1421
WANG Ting, WEN Hui, CUI Hua-qing, YIN Da-li. Research progress on indoleamine 2,3-dioxygenase 1 (IDO1) inhibitorsJ. Acta Pharmaceutica Sinica, 2021,56(3): 723-733. doi: 10.16438/j.0513-4870.2020-1421
Citation: WANG Ting, WEN Hui, CUI Hua-qing, YIN Da-li. Research progress on indoleamine 2,3-dioxygenase 1 (IDO1) inhibitorsJ. Acta Pharmaceutica Sinica, 2021,56(3): 723-733. doi: 10.16438/j.0513-4870.2020-1421

吲哚胺2,3-双加氧酶1(IDO1)抑制剂的研究进展

Research progress on indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors

  • 摘要: 吲哚胺2,3-双加氧酶1(indoleamine 2,3-dioxygenase 1,IDO1)是代谢色氨酸转化为犬尿氨酸的限速酶。其在肿瘤组织中过表达,造成肿瘤微环境中的色氨酸耗竭,从而抑制T细胞功能,介导肿瘤的免疫逃逸,是潜在的肿瘤免疫治疗靶点。目前,多个IDO1抑制剂处于临床研究阶段。本文主要介绍IDO1介导肿瘤免疫逃逸的机制,并根据已报道IDO1抑制剂的结构类型进行分类总结和构效关系简析。

     

    Abstract: Indoleamine 2,3-dioxygenase 1 (IDO1) is the rate-limiting enzyme in the degradation of tryptophan to kynurenine. IDO1 is highly expressed in some tumor tissues. IDO1 can deplete tryptophan in tumor microenvironment, inhibit T cell function, and mediate the immune escape of tumor cells. Thus, IDO1 is considered a potential target of tumor immunotherapy. Currently, there are several IDO1 inhibitors in clinical research studies. The mechanism of IDO1-mediated tumor immune escape and the structure of IDO1 inhibitors are summarized in this review.

     

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