Metabolic Impact of Immune-Suppressor Cells in Cancer Patients

M. Shibata, A. Inukai, Daigo Yoshimori, M. Ashizawa, T. Nakajima, Makoto Takada, T. Yazawa, K. Mimura, N. Inoue, Takafumi Watanabe, Kazunos .
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引用次数: 1

Abstract

Immune checkpoint inhibitors (ICIs) are not equally effective for all patients, regardless type of cancer. Immune-suppressor cells, including regulatory T tumor and their metabolic microenvironment (TME) play important roles in resistance to ICIs. Although Treg cells, TAMs and MDSCs play significant roles in immunosuppression in the TME, these cells are very important in the orchestration of metabolism such as angiogenesis and production of indoleamine 2,3-dioxygenase (IDO) and nitric oxide (NO) towards tumor escape, progression and expansion. Cancer immunotherapies tailored with metabolic characterizations such as parameters of angiogenesis, inflammation or obesity may be needed for the establishment of a successful treatment modality in the immunotherapy era.
免疫抑制细胞对癌症患者代谢的影响
免疫检查点抑制剂(ICIs)并非对所有患者都同样有效,无论癌症类型如何。免疫抑制细胞,包括调节性T肿瘤及其代谢微环境(TME)在ICIs耐药中发挥重要作用。尽管Treg细胞、TAMs和MDSCs在TME的免疫抑制中发挥着重要作用,但这些细胞在协调代谢(如血管生成、吲哚胺2,3-双加氧酶(IDO)和一氧化氮(NO)的产生)以促进肿瘤的逃逸、进展和扩张中发挥着重要作用。在免疫治疗时代,可能需要根据代谢特征(如血管生成、炎症或肥胖参数)量身定制癌症免疫疗法,以建立成功的治疗模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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