用于肿瘤免疫治疗的声动力纳米lytacs逆转肿瘤免疫抑制微环境

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Mengke Xu, Yuxuan Hu, Jiayan Wu, Jing Liu and Kanyi Pu*, 
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引用次数: 0

摘要

细胞外蛋白和跨膜蛋白占肿瘤中所有蛋白质编码基因的约40%,在形成肿瘤免疫抑制微环境(TIME)中起着至关重要的作用。虽然蛋白质降解疗法已经应用于癌细胞的膜蛋白,但很少扩展到免疫细胞。本文报道了一种靶向嵌合体的聚合纳米溶酶体(nano-LYTAC),它在M2巨噬细胞上进行膜蛋白降解,并产生声动力效应,用于联合癌症免疫治疗。与传统抑制剂相比,纳米lytac对白细胞介素4受体(IL-4R)具有更高的降解效率。更重要的是,揭示了纳米lytac对M2巨噬细胞功能的影响具有浓度依赖性:低浓度时下调M2巨噬细胞CD206表达和白细胞介素10 (IL-10)分泌,高浓度时触发M2巨噬细胞凋亡。此外,纳米lytac被发现具有长时间的肿瘤滞留(48小时),允许用一次剂量进行多次声动力治疗。在临床前动物模型中,这种由纳米lytac介导的协同声动力免疫疗法通过抑制M2巨噬细胞和调节性T细胞(Tregs)的功能,促进树突状细胞(dc)的成熟和T效应细胞(Teffs)的肿瘤浸润,有效地重编程TIME,完全抑制肿瘤生长,抑制肺转移,防止复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sonodynamic Nano-LYTACs Reverse Tumor Immunosuppressive Microenvironment for Cancer Immunotherapy

Extracellular and transmembrane proteins, which account for the products of approximately 40% of all protein-encoding genes in tumors, play a crucial role in shaping the tumor immunosuppressive microenvironment (TIME). While protein degradation therapy has been applied to membrane proteins of cancer cells, it has rarely been extended to immune cells. We herein report a polymeric nanolysosome targeting chimera (nano-LYTAC) that undergoes membrane protein degradation on M2 macrophages and generates a sonodynamic effect for combinational cancer immunotherapy. Nano-LYTAC is found to have higher degradation efficacy to the interleukin 4 receptor (IL-4R) compared to traditional inhibitors. More importantly, it is revealed that the effect of nano-LYTAC on the function of the M2 macrophage is concentration-dependent: downregulating CD206 expression and interleukin 10 (IL-10) secretion from M2 macrophages at low concentration, while triggering their apoptosis at high concentration. Moreover, nano-LYTAC is found to possess long tumor retention (>48 h), allowing for multiple sonodynamic treatments with a single dose. Such a synergistic sonodynamic immunotherapy mediated by nano-LYTAC effectively reprograms the TIME via inhibiting the functions of M2 macrophages and regulatory T cells (Tregs), as well as promoting the maturation of dendritic cells (DCs) and tumor infiltration of T effector cells (Teffs), completely suppressing tumor growth, inhibiting pulmonary metastasis, and preventing recurrence under preclinical animal models.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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