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通过逐步饥饿-光热疗法调节免疫记忆并逆转肿瘤耐热性。

Regulating immune memory and reversing tumor thermotolerance through a step-by-step starving-photothermal therapy.

机构信息

College of Pharmaceutical Sciences, Zhejiang University, 866 Yuhangtang Road, Hangzhou, 310058, Zhejiang, People's Republic of China.

Department of Respiratory Disease, Zhejiang Provincial People's Hospital, Hangzhou, 310003, Zhejiang, China.

出版信息

J Nanobiotechnology. 2021 Sep 30;19(1):297. doi: 10.1186/s12951-021-01011-2.

Abstract

BACKGROUND

Photothermal therapy (PTT) is a highly effective treatment for solid tumors and can induce long-term immune memory worked like an in situ vaccine. Nevertheless, PTT inevitably encounters photothermal resistance of tumor cells, which hinders therapeutic effect or even leads to tumor recurrence. Naïve CD8+ T cells are mainly metabolized by oxidative phosphorylation (OXPHOS), followed by aerobic glycolysis after activation. And the differentiate of effector CD8+ T cell (CD8+ T) into central memory CD8+ T cell (CD8+ TCM) depends on fatty acid oxidation (FAO) to meet their metabolic requirements, which is regulated by adenosine monophosphate activated protein kinase (AMPK). In addition, the tumor microenvironment (TME) is severely immunosuppressive, conferring additional protection against the host immune response mediated by PTT.

METHODS

Metformin (Met) down-regulates NADH/NADPH, promotes the FAO of CD8+ T cells by activating AMPK, increases the number of CD8+ TCM, which boosts the long-term immune memory of tumor-bearing mice treated with PTT. Here, a kind of PLGA microspheres co-encapsulated hollow gold nanoshells and Met (HAuNS-Met@MS) was constructed to inhibit the tumor progress. 2-Deoxyglucose (2DG), a glycolysis inhibitor for cancer starving therapy, can cause energy loss of tumor cells, reduce the heat stress response of tumor cell, and reverse its photothermal resistance. Moreover, 2DG prevents N-glycosylation of proteins that cause endoplasmic reticulum stress (ERS), further synergistically enhance PTT-induced tumor immunogenic cell death (ICD), and improve the effect of immunotherapy. So 2DG was also introduced and optimized here to solve the metabolic competition among tumor cells and immune cells in the TME.

RESULTS

We utilized mild PTT effect of HAuNS to propose an in situ vaccine strategy based on the tumor itself. By targeting the metabolism of TME with different administration strategy of 2DG and perdurable action of Met, the thermotolerance of tumor cells was reversed, more CD8+ TCMs were produced and more effective anti-tumor was presented in this study.

CONCLUSION

The Step-by-Step starving-photothermal therapy could not only reverse the tumor thermotolerance, but also enhance the ICD and produce more CD8+ TCM during the treatment.

摘要

背景

光热疗法(PTT)是治疗实体瘤的一种非常有效的方法,可诱导类似于原位疫苗的长期免疫记忆。然而,PTT 不可避免地会遇到肿瘤细胞的光热抗性,这会阻碍治疗效果,甚至导致肿瘤复发。初始 CD8+T 细胞主要通过氧化磷酸化(OXPHOS)代谢,然后在激活后进行有氧糖酵解。效应 CD8+T 细胞(CD8+T)分化为中央记忆 CD8+T 细胞(CD8+TCM)取决于脂肪酸氧化(FAO)以满足其代谢需求,这受 AMP 激活蛋白激酶(AMPK)调节。此外,肿瘤微环境(TME)严重免疫抑制,赋予了对 PTT 介导的宿主免疫反应的额外保护。

方法

二甲双胍(Met)通过激活 AMPK 下调 NADH/NADPH,促进 CD8+T 细胞的 FAO,增加 CD8+TCM 的数量,从而增强接受 PTT 治疗的荷瘤小鼠的长期免疫记忆。在这里,构建了一种共包封空心金纳米壳和二甲双胍(HAuNS-Met@MS)的 PLGA 微球来抑制肿瘤进展。2-脱氧葡萄糖(2DG)是一种用于癌症饥饿治疗的糖酵解抑制剂,可导致肿瘤细胞能量损失,降低肿瘤细胞的热应激反应,并逆转其光热抗性。此外,2DG 可防止引起内质网应激(ERS)的蛋白质的 N-糖基化,进一步协同增强 PTT 诱导的肿瘤免疫原性细胞死亡(ICD),并提高免疫治疗效果。因此,这里也引入并优化了 2DG 以解决 TME 中肿瘤细胞和免疫细胞之间的代谢竞争。

结果

我们利用 HAuNS 的温和 PTT 效应,提出了一种基于肿瘤本身的原位疫苗策略。通过针对 TME 的代谢,采用不同的 2DG 给药策略和二甲双胍的持久作用,逆转了肿瘤细胞的热耐受性,产生了更多的 CD8+TCM,并在本研究中表现出更有效的抗肿瘤作用。

结论

分步饥饿-光热疗法不仅可以逆转肿瘤的热耐受性,而且可以在治疗过程中增强 ICD 并产生更多的 CD8+TCM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68c3/8482573/80d77e851378/12951_2021_1011_Sch1_HTML.jpg

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