Bad Cholesterol Uptake by CD36 in T-Cells Cripples Anti-Tumor Immune Response.

Immunometabolism Pub Date : 2021-01-01 Epub Date: 2021-09-14 DOI:10.20900/immunometab20210028
Mikhail G Kolonin
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引用次数: 5

Abstract

Despite the advances in immunotherapies, effective against some types of cancer, progression of several types of carcinoma remains uncurable. Recent studies indicate that changes in lipid metabolism, aggravated by obesity, disable anti-tumor immune response. In the July issue of Immunity, Xu et al. use mouse models to demonstrate that certain types of oxidized lipids, transported by CD36, suppress the capacity of CD8+ T lymphocytes to secrete cytotoxic molecules. This study sheds light on how lipid modifications in the tumor microenvironment make killer T cells incapable of inhibiting tumor growth.

CD36在t细胞中的不良胆固醇摄取削弱抗肿瘤免疫反应
尽管免疫疗法取得了进展,对某些类型的癌症有效,但一些类型的癌症的进展仍然无法治愈。最近的研究表明,脂质代谢的变化,肥胖加剧,使抗肿瘤免疫反应失效。在7月出版的《免疫》杂志上,Xu等人用小鼠模型证明了某些类型的氧化脂质,由CD36运输,抑制CD8+ T淋巴细胞分泌细胞毒性分子的能力。这项研究揭示了肿瘤微环境中的脂质修饰如何使杀伤T细胞无法抑制肿瘤生长。
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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