• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

纳米材料辅助递送 CpG 寡脱氧核苷酸以增强癌症免疫治疗。

Nanomaterial-assisted delivery of CpG oligodeoxynucleotides for boosting cancer immunotherapy.

机构信息

Department of Pharmacology, Beijing Chest Hospital, Capital Medical University/Beijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.

Department of Pharmacology, Beijing Chest Hospital, Capital Medical University/Beijing Key Laboratory of Drug Resistance Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.

出版信息

J Control Release. 2024 Dec;376:184-199. doi: 10.1016/j.jconrel.2024.09.044. Epub 2024 Oct 11.

DOI:10.1016/j.jconrel.2024.09.044
PMID:39368710
Abstract

Cancer immunotherapy aims to improve immunity to not only eliminate the primary tumor but also inhibit metastasis and recurrence. It is considered an extremely promising therapeutic approach that breaks free from the traditional paradigm of oncological treatment. As the medical community learns more about the immune system's mechanisms that "turn off the brake" and "step on the throttle", there is increasingly successful research on immunomodulators. However, there are still more restrictions than countermeasures with immunotherapy related to immunomodulators, such as low responsiveness and immune-related adverse events that cause multiple adverse reactions. Therefore, medical experts and materials scientists attempted to the efficacy of immunomodulatory treatments through various methods, especially nanomaterial-assisted strategies. CpG oligodeoxynucleotides (CpG) not only act as an adjuvant to promote immune responses, but also induce autophagy. In this review, the enhancement of immunotherapy using nanomaterial-based CpG formulations is systematically elaborated, with a focus on the delivery, protection, synergistic promotion of CpG efficacy by nanomaterials, and selection of the timing of treatment. In addition, we also discuss and prospect the existing problems and future directions of research on nanomaterials in auxiliary CpG therapy.

摘要

癌症免疫疗法旨在提高免疫力,不仅消除原发肿瘤,还能抑制转移和复发。它被认为是一种极具前景的治疗方法,打破了传统的肿瘤治疗模式。随着医学界对免疫系统“松开刹车”和“踩油门”机制的了解越来越多,免疫调节剂的研究也越来越成功。然而,与免疫调节剂相关的免疫疗法仍然存在更多的限制,例如低反应性和免疫相关的不良反应导致多种不良反应。因此,医学专家和材料科学家试图通过各种方法来提高免疫调节剂治疗的疗效,特别是纳米材料辅助策略。CpG 寡脱氧核苷酸(CpG)不仅可以作为佐剂促进免疫反应,还可以诱导自噬。在这篇综述中,系统地阐述了基于纳米材料的 CpG 制剂在免疫治疗中的增强作用,重点介绍了纳米材料在 CpG 传递、保护、协同增效以及治疗时机选择方面的作用。此外,我们还讨论并展望了纳米材料在 CpG 辅助治疗中的现有问题和未来研究方向。

相似文献

1
Nanomaterial-assisted delivery of CpG oligodeoxynucleotides for boosting cancer immunotherapy.纳米材料辅助递送 CpG 寡脱氧核苷酸以增强癌症免疫治疗。
J Control Release. 2024 Dec;376:184-199. doi: 10.1016/j.jconrel.2024.09.044. Epub 2024 Oct 11.
2
CpG oligodeoxynucleotides for immune stimulation in cancer immunotherapy.用于癌症免疫治疗中免疫刺激的CpG寡脱氧核苷酸
Curr Opin Investig Drugs. 2003 Jun;4(6):686-90.
3
Immune lipoprotein nanostructures inspired relay drug delivery for amplifying antitumor efficiency.免疫脂蛋白纳米结构启发的接力式药物递送用于增强抗肿瘤效率。
Biomaterials. 2018 Dec;185:205-218. doi: 10.1016/j.biomaterials.2018.09.016. Epub 2018 Sep 13.
4
Mannose-Modified Liposome Co-Delivery of Human Papillomavirus Type 16 E7 Peptide and CpG Oligodeoxynucleotide Adjuvant Enhances Antitumor Activity Against Established Large TC-1 Grafted Tumors in Mice.甘露糖修饰脂质体共递送人乳头瘤病毒 16 型 E7 肽和 CpG 寡脱氧核苷酸佐剂增强了对小鼠已建立的大 TC-1 移植瘤的抗肿瘤活性。
Int J Nanomedicine. 2020 Dec 1;15:9571-9586. doi: 10.2147/IJN.S275670. eCollection 2020.
5
Dual TLR agonist nanodiscs as a strong adjuvant system for vaccines and immunotherapy.双 TLR 激动剂纳米盘作为疫苗和免疫疗法的强佐剂系统。
J Control Release. 2018 Jul 28;282:131-139. doi: 10.1016/j.jconrel.2018.04.041. Epub 2018 Apr 25.
6
Noninvasive and efficient transdermal delivery of CpG-oligodeoxynucleotide for cancer immunotherapy.非侵入性、高效的经皮传递 CpG-寡脱氧核苷酸用于癌症免疫治疗。
J Control Release. 2011 Mar 30;150(3):256-65. doi: 10.1016/j.jconrel.2011.01.018. Epub 2011 Jan 21.
7
Lipid-based delivery of CpG oligonucleotides enhances immunotherapeutic efficacy.基于脂质的CpG寡核苷酸递送可增强免疫治疗效果。
Adv Drug Deliv Rev. 2009 Mar 28;61(3):233-42. doi: 10.1016/j.addr.2008.12.014. Epub 2009 Feb 13.
8
Glatiramer Acetate Complexed with CpG as Intratumoral Immunotherapy in Combination with Anti-PD-1.醋酸格拉替雷与 CpG 复合物作为瘤内免疫疗法联合抗 PD-1 治疗。
Mol Pharm. 2022 Nov 7;19(11):4357-4369. doi: 10.1021/acs.molpharmaceut.2c00730. Epub 2022 Oct 25.
9
Liposomal CpG-ODN: An in vitro and in vivo study on macrophage subtypes responses, biodistribution and subsequent therapeutic efficacy in mice models of cancers.脂质体 CpG-ODN:在体外和体内研究巨噬细胞亚型反应、生物分布以及在癌症小鼠模型中的后续治疗效果。
Eur J Pharm Sci. 2018 Jul 1;119:159-170. doi: 10.1016/j.ejps.2018.04.018. Epub 2018 Apr 13.
10
Carbonate Apatite Nanoparticles Act as Potent Vaccine Adjuvant Delivery Vehicles by Enhancing Cytokine Production Induced by Encapsulated Cytosine-Phosphate-Guanine Oligodeoxynucleotides.碳酸磷灰石纳米颗粒通过增强包裹的胞嘧啶-磷酸-鸟嘌呤寡脱氧核苷酸诱导的细胞因子产生,充当有效的疫苗佐剂递送载体。
Front Immunol. 2018 Apr 18;9:783. doi: 10.3389/fimmu.2018.00783. eCollection 2018.

引用本文的文献

1
Nanomaterial-based encapsulation of biochemicals for targeted sepsis therapy.基于纳米材料的生化物质封装用于靶向性脓毒症治疗。
Mater Today Bio. 2025 Jul 4;33:102054. doi: 10.1016/j.mtbio.2025.102054. eCollection 2025 Aug.
2
Fabrication of RIG-I-Activating Nanoparticles for Intratumoral Immunotherapy via Flash Nanoprecipitation.通过快速纳米沉淀法制备用于肿瘤内免疫治疗的RIG-I激活纳米颗粒
Mol Pharm. 2025 Aug 4;22(8):4597-4611. doi: 10.1021/acs.molpharmaceut.5c00125. Epub 2025 Jul 1.
3
Aptamer-ODN Chimeras: Enabling Cell-Specific ODN Targeting Therapy.
适体-寡核苷酸嵌合体:实现细胞特异性寡核苷酸靶向治疗。
Cells. 2025 May 12;14(10):697. doi: 10.3390/cells14100697.
4
Metal coordination polymer nanoparticles for cancer therapy.用于癌症治疗的金属配位聚合物纳米颗粒。
Essays Biochem. 2025 Apr 10;69(2):EBC20253012. doi: 10.1042/EBC20253012.