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吲哚胺 2,3-双加氧酶(IDO)抑制作为增强癌症免疫治疗的策略。

Indoleamine 2,3-Dioxygenase (IDO) Inhibition as a Strategy to Augment Cancer Immunotherapy.

机构信息

Division of Hematology/Oncology, Department of Internal Medicine, University of Michigan Health System, 1500 E. Medical Center Drive, C369 Med Inn Building, SPC 5848, Ann Arbor, MI, 48109, USA.

出版信息

BioDrugs. 2018 Aug;32(4):311-317. doi: 10.1007/s40259-018-0291-4.

Abstract

Indoleamine 2,3-dioxygenase (IDO) is an enzyme of interest in immuno-oncology because of the immunosuppressive effects that result from its role in tryptophan catabolism. IDO is upregulated in malignancy and is associated with poor prognosis in multiple cancer types. IDO inhibitors have been developed to target IDO, both directly and indirectly. Pre-clinical data have shown combined IDO and checkpoint inhibition to be an efficacious strategy for tumor control. Clinical trials of IDO inhibitors with chemotherapy or immunotherapy are currently underway. This review describes the function of IDO and its inhibitors and summarizes the efficacy and toxicity data from recent clinical trials with these drugs.

摘要

吲哚胺 2,3-双加氧酶 (IDO) 是免疫肿瘤学中引人关注的一种酶,因为其在色氨酸分解代谢中的作用会产生免疫抑制效应。IDO 在恶性肿瘤中上调,并与多种癌症类型的不良预后相关。已经开发出 IDO 抑制剂来靶向 IDO,包括直接和间接靶向。临床前数据表明,联合 IDO 和检查点抑制是控制肿瘤的有效策略。目前正在进行 IDO 抑制剂与化疗或免疫疗法联合的临床试验。本文描述了 IDO 及其抑制剂的功能,并总结了这些药物近期临床试验的疗效和毒性数据。

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