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IDO1 在癌症中的作用:免疫检查点的双子座。

IDO1 in cancer: a Gemini of immune checkpoints.

机构信息

Department of Neurological Surgery, Northwestern University, Chicago, USA.

Department of Pediatrics, Northwestern University, Chicago, USA.

出版信息

Cell Mol Immunol. 2018 May;15(5):447-457. doi: 10.1038/cmi.2017.143. Epub 2018 Jan 29.

DOI:10.1038/cmi.2017.143
PMID:29375124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6068130/
Abstract

Indoleamine 2, 3-dioxygenase 1 (IDO1) is a rate-limiting metabolic enzyme that converts the essential amino acid tryptophan (Trp) into downstream catabolites known as kynurenines. Coincidently, numerous studies have demonstrated that IDO1 is highly expressed in multiple types of human cancer. Preclinical studies have further introduced an interesting paradox: while single-agent treatment with IDO1 enzyme inhibitor has a negligible effect on decreasing the established cancer burden, approaches combining select therapies with IDO1 blockade tend to yield a synergistic benefit against tumor growth and/or animal subject survival. Given the high expression of IDO1 among multiple cancer types along with the lack of monotherapeutic efficacy, these data suggest that there is a more complex mechanism of action than previously appreciated. Similar to the dual faces of the astrological Gemini, we highlight the multiple roles of IDO1 and review its canonical association with IDO1-dependent tryptophan metabolism, as well as documented evidence confirming the dispensability of enzyme activity for its immunosuppressive effects. The gene transcript levels for IDO1 highlight its strong association with T-cell infiltration, but the lack of a universal prognostic significance among all cancer subtypes. Finally, ongoing clinical trials are discussed with consideration of IDO1-targeting strategies that enhance the efficacy of immunotherapy for cancer patients.

摘要

吲哚胺 2,3-双加氧酶 1(IDO1)是一种限速代谢酶,可将必需氨基酸色氨酸(Trp)转化为下游代谢产物犬尿氨酸。巧合的是,大量研究表明 IDO1 在多种人类癌症中高度表达。临床前研究进一步引入了一个有趣的悖论:虽然单独使用 IDO1 酶抑制剂治疗对减少已建立的癌症负担几乎没有影响,但将选择性治疗方法与 IDO1 阻断相结合的方法往往会对肿瘤生长和/或动物存活产生协同益处。鉴于 IDO1 在多种癌症类型中的高表达以及单一疗法疗效的缺乏,这些数据表明存在比以前认识到的更复杂的作用机制。类似于占星术中的双子座的两面性,我们强调了 IDO1 的多种作用,并回顾了其与 IDO1 依赖性色氨酸代谢的经典关联,以及证实酶活性对其免疫抑制作用的非必要性的已有证据。IDO1 的基因转录水平突出了其与 T 细胞浸润的强烈关联,但并非所有癌症亚型都具有普遍的预后意义。最后,讨论了正在进行的临床试验,并考虑了针对 IDO1 的靶向策略,以提高癌症患者免疫疗法的疗效。

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本文引用的文献

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The Aryl Hydrocarbon Receptor Preferentially Marks and Promotes Gut Regulatory T Cells.芳香烃受体优先标记和促进肠道调节性 T 细胞。
Cell Rep. 2017 Nov 21;21(8):2277-2290. doi: 10.1016/j.celrep.2017.10.114.
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Concurrent PD-1 Blockade Negates the Effects of OX40 Agonist Antibody in Combination Immunotherapy through Inducing T-cell Apoptosis.OX40 激动剂抗体联合免疫疗法中 PD-1 阻断通过诱导 T 细胞凋亡而失效。
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Infiltrating T Cells Increase IDO1 Expression in Glioblastoma and Contribute to Decreased Patient Survival.浸润 T 细胞增加胶质母细胞瘤中 IDO1 的表达,并导致患者生存时间缩短。
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Preparation and evaluation of L- and D-5-[F]fluorotryptophan as PET imaging probes for indoleamine and tryptophan 2,3-dioxygenases.L-和D-5-[F]氟色氨酸作为吲哚胺和色氨酸2,3-双加氧酶PET成像探针的制备与评价
Nucl Med Biol. 2017 Aug;51:10-17. doi: 10.1016/j.nucmedbio.2017.05.001. Epub 2017 May 5.
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Blockade of IDO-kynurenine-AhR metabolic circuitry abrogates IFN-γ-induced immunologic dormancy of tumor-repopulating cells.阻断 IDO-犬尿氨酸-AhR 代谢通路可消除 IFN-γ 诱导的肿瘤再生细胞免疫休眠。
Nat Commun. 2017 May 10;8:15207. doi: 10.1038/ncomms15207.
6
Non-tumor cell IDO1 predominantly contributes to enzyme activity and response to CTLA-4/PD-L1 inhibition in mouse glioblastoma.非肿瘤细胞 IDO1 主要促进了 CTLA-4/PD-L1 抑制在小鼠脑胶质瘤中的酶活性和反应。
Brain Behav Immun. 2017 May;62:24-29. doi: 10.1016/j.bbi.2017.01.022. Epub 2017 Feb 4.
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First-in-Human Phase I Study of the Oral Inhibitor of Indoleamine 2,3-Dioxygenase-1 Epacadostat (INCB024360) in Patients with Advanced Solid Malignancies.首个人体 I 期研究:口服吲哚胺 2,3-双加氧酶-1 抑制剂 Epacadostat(INCB024360)治疗晚期实体瘤患者。
Clin Cancer Res. 2017 Jul 1;23(13):3269-3276. doi: 10.1158/1078-0432.CCR-16-2272. Epub 2017 Jan 4.
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Improved Radiosynthesis and Biological Evaluations of L- and D-1-[F]Fluoroethyl-Tryptophan for PET Imaging of IDO-Mediated Kynurenine Pathway of Tryptophan Metabolism.用于吲哚胺2,3-双加氧酶介导的色氨酸代谢犬尿氨酸途径PET成像的L-和D-1-[F]氟乙基色氨酸的改进放射性合成及生物学评价
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Advanced age negatively impacts survival in an experimental brain tumor model.在一个实验性脑肿瘤模型中,高龄对生存率有负面影响。
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A phase I study of indoximod in patients with advanced malignancies.吲哚莫德用于晚期恶性肿瘤患者的I期研究。
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