Multi-modal Ca2+ nanogenerator via reversing T cell exhaustion for enhanced chemo-immunotherapy

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jingyi An , Rong Guo , Mengyuan Liu , Haiying Hu , Hongling Zhang
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引用次数: 0

Abstract

Chemo-immunotherapy holds the advantage of specific antitumor effects by activating cytotoxic lymphocyte cells (CTLs) immune response. However, multiple barriers have limited the outcomes partly due to tumor-cell-mediated exhaustion of CTLs in the immunosuppressive tumor microenvironment (iTME). Here, we rationally designed a simple-yet-versatile Ca2+ nanogenerator to modulate iTME for enhancing 2-deoxyglucose (2-DG) mediated chemo-immunotherapy. Briefly, after 2-DG chemotherapy, CaO2 nanoparticles coated with EL4 cell membrane (denoted as CaNP@ECM) could preferentially accumulate in tumor tissue via adhesion between LFA-1 on EL4 cell membrane and ICAM-1 on inflamed endothelial cell in tumor tissues and display a series of benefits for CTLs: i) Increasing glucose availability of CTLs while reducing lactic acid secretion through Ca2+ overloading mediated inhibition of tumor cell glycolysis, as well as relieving hypoxia; ii) Reversing CTLs exhaustion via TGF-β1 scavenging and PD-L1 blockade through PD-1 and TGF-β1R on EL4 cell membrane; iii) Boosting tumor immunotherapy via immunologic death (ICD) of tumor cells induced by Ca2+ overloading. We demonstrate that the multi-modal Ca2+ nanogenerator rescues T cells from exhaustion and inhibits tumor growth both in vitro and in vivo. More importantly, the study also facilitate the development of glucose metabolism inhibition-based tumor immunotherapy via Ca2+ overloading.

Abstract Image

通过逆转 T 细胞衰竭增强化疗免疫疗法的多模式 Ca2+ 纳米发电机
化学免疫疗法的优势在于通过激活细胞毒性淋巴细胞(CTLs)的免疫反应产生特异性抗肿瘤效果。然而,由于肿瘤细胞介导的 CTLs 在免疫抑制性肿瘤微环境(iTME)中耗竭,多重障碍限制了化疗的效果。在这里,我们合理地设计了一种简单但易变的 Ca2+ 纳米发生器来调节 iTME,以增强 2-DG 介导的化疗免疫疗法。简言之,2-DG 化疗后,包覆 EL4 细胞膜的 CaO2 纳米粒子(CaNP@ECM)可通过 EL4 细胞膜上的 LFA-1 与肿瘤组织中发炎内皮细胞上的 ICAM-1 之间的粘附作用,优先在肿瘤组织中聚集,并对 CTL 产生一系列益处:i) 通过 Ca2+ 超载介导的肿瘤细胞糖酵解抑制,增加 CTLs 的葡萄糖可用性,同时减少乳酸分泌,缓解缺氧;ii) 通过 TGF-β1 清除和通过 EL4 细胞膜上的 PD-1 和 TGF-β1R 阻断 PD-L1,逆转 CTLs 的衰竭;iii) 通过 Ca2+ 超载诱导的肿瘤细胞免疫死亡(ICD),促进肿瘤免疫治疗。我们证明,多模式 Ca2+ 纳米发生器能在体外和体内挽救衰竭的 T 细胞并抑制肿瘤生长。更重要的是,这项研究还促进了通过 Ca2+ 过载抑制葡萄糖代谢的肿瘤免疫疗法的发展。
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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