基于吲哚胺2,3双加氧酶抑制剂的肿瘤免疫治疗综述

Xiangyu Hao
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引用次数: 1

摘要

肿瘤免疫治疗因其具有良好的临床疗效而成为科研人员最关注的领域和方向之一。尽管仍有许多生物医学障碍阻碍了这种治疗的有效性。吲哚胺2,3双加氧酶(IDO)是肿瘤微环境的关键抑制因子。因此,在一些临床前研究中,IDO的抑制是非常有效的,一些IDO抑制剂正在临床研究中。此外,基于碘的纳米给药系统在抗癌治疗中发挥着重要作用。本文综述了肿瘤微环境、IDO抑制剂和纳米药物递送系统在肿瘤免疫治疗中的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overview of Tumor Immunotherapy based on Indoleamine 2,3 Dioxygenase Inhibitors
Tumor immunotherapy is one of the most attractive fields and direction for scientific researchers due to its promising clinical efficacy. While there are still many biomedical obstacles hindering the efficacy of this treatment. Indoleamine 2,3 dioxygenase (IDO) is a key suppressive factor in the tumor microenvironment. Therefore, Inhibition of IDO is strongly effective in some preclinical researches and some IDO inhibitors are in clinical research now. Moreover, IDO-based nano-drug delivery system in anticancer therapy is playing important role. The tumor microenvironment and current research progress of IDO inhibitors and nano-drug delivery systems in tumor immunotherapy are illustrated in this review.
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