• 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

基于纳米颗粒的嵌合抗原受体疗法在癌症免疫治疗中的应用。

Nanoparticle-Based Chimeric Antigen Receptor Therapy for Cancer Immunotherapy.

机构信息

Department of Integrative Biotechnology, College of Biotechnology and Bioengineering, Sungkyunkwan University, Seobu-ro 2066, Suwon, Gyeonggi, 16419, Republic of Korea.

Department of Global Biomedical Engineering, SKKU Institute for Convergence, Sungkyunkwan University (SKKU), Seobu-ro 2066, Suwon, Gyeonggi, 16419, Republic of Korea.

出版信息

Tissue Eng Regen Med. 2023 Jun;20(3):371-387. doi: 10.1007/s13770-022-00515-8. Epub 2023 Mar 3.

DOI:10.1007/s13770-022-00515-8
PMID:36867402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9983528/
Abstract

Adoptive cell therapy with chimeric antigen receptor (CAR)-engineered T cells (CAR-Ts) has emerged as an innovative immunotherapy for hematological cancer treatment. However, the limited effect on solid tumors, complex processes, and excessive manufacturing costs remain as limitations of CAR-T therapy. Nanotechnology provides an alternative to the conventional CAR-T therapy. Owing to their unique physicochemical properties, nanoparticles can not only serve as a delivery platform for drugs but also target specific cells. Nanoparticle-based CAR therapy can be applied not only to T cells but also to CAR-natural killer and CAR-macrophage, compensating for some of their limitations. This review focuses on the introduction of nanoparticle-based advanced CAR immune cell therapy and future perspectives on immune cell reprogramming.

摘要

嵌合抗原受体 (CAR)-修饰 T 细胞 (CAR-T) 的过继细胞疗法已成为血液系统恶性肿瘤治疗的一种创新免疫疗法。然而,CAR-T 治疗的局限性在于对实体瘤的疗效有限、过程复杂且制造成本过高。纳米技术为传统 CAR-T 治疗提供了一种替代方法。由于其独特的物理化学性质,纳米粒子不仅可以作为药物的递送平台,还可以靶向特定的细胞。基于纳米粒子的 CAR 疗法不仅可以应用于 T 细胞,还可以应用于 CAR-自然杀伤细胞和 CAR-巨噬细胞,弥补了它们的一些局限性。本综述重点介绍了基于纳米粒子的先进 CAR 免疫细胞疗法,并对免疫细胞重编程的未来前景进行了展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/90db66b209e6/13770_2022_515_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/bf8493aee04d/13770_2022_515_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/3865da8f7d16/13770_2022_515_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/79b7094bf7b9/13770_2022_515_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/06b03e2dadb0/13770_2022_515_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/ad2dd4b7eacb/13770_2022_515_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/39f25705d325/13770_2022_515_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/d09abc76e314/13770_2022_515_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/5614827c4ef5/13770_2022_515_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/90db66b209e6/13770_2022_515_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/bf8493aee04d/13770_2022_515_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/3865da8f7d16/13770_2022_515_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/79b7094bf7b9/13770_2022_515_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/06b03e2dadb0/13770_2022_515_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/ad2dd4b7eacb/13770_2022_515_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/39f25705d325/13770_2022_515_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/d09abc76e314/13770_2022_515_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/5614827c4ef5/13770_2022_515_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66a/10219915/90db66b209e6/13770_2022_515_Fig9_HTML.jpg

相似文献

1
Nanoparticle-Based Chimeric Antigen Receptor Therapy for Cancer Immunotherapy.基于纳米颗粒的嵌合抗原受体疗法在癌症免疫治疗中的应用。
Tissue Eng Regen Med. 2023 Jun;20(3):371-387. doi: 10.1007/s13770-022-00515-8. Epub 2023 Mar 3.
2
Nanotechnology and immunoengineering: How nanotechnology can boost CAR-T therapy.纳米技术与免疫工程:纳米技术如何增强 CAR-T 疗法
Acta Biomater. 2020 Jun;109:21-36. doi: 10.1016/j.actbio.2020.04.015. Epub 2020 Apr 13.
3
Innate and Innate-Like Cells: The Future of Chimeric Antigen Receptor (CAR) Cell Therapy.先天和类先天细胞:嵌合抗原受体 (CAR) 细胞治疗的未来。
Trends Pharmacol Sci. 2021 Jan;42(1):45-59. doi: 10.1016/j.tips.2020.11.004. Epub 2020 Nov 26.
4
Adoptive cellular immunotherapy for solid neoplasms beyond CAR-T.实体瘤过继细胞免疫治疗:除 CAR-T 以外的方法
Mol Cancer. 2023 Feb 7;22(1):28. doi: 10.1186/s12943-023-01735-9.
5
CAR race to cancer immunotherapy: from CAR T, CAR NK to CAR macrophage therapy.嵌合抗原受体(CAR)在癌症免疫疗法中的竞赛:从 CAR T、CAR NK 到 CAR 巨噬细胞疗法。
J Exp Clin Cancer Res. 2022 Mar 31;41(1):119. doi: 10.1186/s13046-022-02327-z.
6
In Vitro-Transcribed mRNA Chimeric Antigen Receptor T Cell (IVT mRNA CAR T) Therapy in Hematologic and Solid Tumor Management: A Preclinical Update.体外转录信使 RNA 嵌合抗原受体 T 细胞(IVT mRNA CAR T)疗法在血液系统恶性肿瘤和实体瘤治疗中的临床前进展。
Int J Mol Sci. 2020 Sep 6;21(18):6514. doi: 10.3390/ijms21186514.
7
Chimeric antigen receptor- and natural killer cell receptor-engineered innate killer cells in cancer immunotherapy.嵌合抗原受体和自然杀伤细胞受体修饰的自然杀伤细胞在癌症免疫治疗中的应用。
Cell Mol Immunol. 2021 Sep;18(9):2083-2100. doi: 10.1038/s41423-021-00732-6. Epub 2021 Jul 15.
8
Current progress of chimeric antigen receptor (CAR) T versus CAR NK cell for immunotherapy of solid tumors.嵌合抗原受体(CAR)T 细胞与 CARNK 细胞免疫治疗实体瘤的研究进展。
Life Sci. 2024 Jan 15;337:122381. doi: 10.1016/j.lfs.2023.122381. Epub 2023 Dec 23.
9
Chimeric Antigen Receptor T Cell Immunotherapy for Tumor: A Review of Patent Literatures.嵌合抗原受体 T 细胞免疫疗法治疗肿瘤:专利文献综述。
Recent Pat Anticancer Drug Discov. 2019;14(1):60-69. doi: 10.2174/1574892814666190111120908.
10
Advances in CAR-Engineered Immune Cell Generation: Engineering Approaches and Sourcing Strategies.嵌合抗原受体工程免疫细胞的进展:工程方法和来源策略。
Adv Sci (Weinh). 2023 Dec;10(35):e2303215. doi: 10.1002/advs.202303215. Epub 2023 Oct 31.

引用本文的文献

1
Emerging CAR immunotherapies: broadening therapeutic horizons beyond cancer.新兴的嵌合抗原受体免疫疗法:拓展癌症以外的治疗视野。
Clin Exp Med. 2025 Aug 4;25(1):274. doi: 10.1007/s10238-025-01820-x.
2
In vivo CAR engineering for immunotherapy.用于免疫治疗的体内CAR工程。
Nat Rev Immunol. 2025 May 16. doi: 10.1038/s41577-025-01174-1.
3
From lab to lifesaver: the rise of CAR T-cell therapy in oncology.从实验室到救命疗法:嵌合抗原受体T细胞疗法在肿瘤学领域的崛起

本文引用的文献

1
Fingolimod-Conjugated Charge-Altering Releasable Transporters Efficiently and Specifically Deliver mRNA to Lymphocytes In Vivo and In Vitro.手性改变电荷型可释放衔接物递药系统有效且特异性地将 mRNA 递送至体内和体外的淋巴细胞
Biomacromolecules. 2022 Jul 11;23(7):2976-2988. doi: 10.1021/acs.biomac.2c00469. Epub 2022 Jun 24.
2
CAR race to cancer immunotherapy: from CAR T, CAR NK to CAR macrophage therapy.嵌合抗原受体(CAR)在癌症免疫疗法中的竞赛:从 CAR T、CAR NK 到 CAR 巨噬细胞疗法。
J Exp Clin Cancer Res. 2022 Mar 31;41(1):119. doi: 10.1186/s13046-022-02327-z.
3
CAR-NK cells for cancer immunotherapy: from bench to bedside.
J Egypt Natl Canc Inst. 2025 May 16;37(1):37. doi: 10.1186/s43046-025-00262-6.
4
Nanoimmunotherapy: the smart trooper for cancer therapy.纳米免疫疗法:癌症治疗的智能勇士。
Explor Target Antitumor Ther. 2025 Apr 10;6:1002308. doi: 10.37349/etat.2025.1002308. eCollection 2025.
5
Nanomaterial-based detection of circulating tumor cells and circulating cancer stem cells for cancer immunotherapy.基于纳米材料的循环肿瘤细胞和循环癌干细胞检测用于癌症免疫治疗。
Nano Converg. 2024 Dec 13;11(1):56. doi: 10.1186/s40580-024-00466-x.
6
Empowering brain tumor management: chimeric antigen receptor macrophage therapy.赋能脑肿瘤管理:嵌合抗原受体巨噬细胞疗法。
Theranostics. 2024 Sep 3;14(14):5725-5742. doi: 10.7150/thno.98290. eCollection 2024.
7
A translational framework to DELIVER nanomedicines to the clinic.一个将纳米药物递送至临床的转化框架。
Nat Nanotechnol. 2024 Nov;19(11):1597-1611. doi: 10.1038/s41565-024-01754-7. Epub 2024 Sep 6.
8
The next frontier in immunotherapy: potential and challenges of CAR-macrophages.免疫疗法的下一个前沿领域:嵌合抗原受体巨噬细胞的潜力与挑战。
Exp Hematol Oncol. 2024 Aug 5;13(1):76. doi: 10.1186/s40164-024-00549-9.
9
Advancements and challenges in developing in vivo CAR T cell therapies for cancer treatment.开发用于癌症治疗的体内 CAR T 细胞疗法的进展和挑战。
EBioMedicine. 2024 Aug;106:105266. doi: 10.1016/j.ebiom.2024.105266. Epub 2024 Aug 1.
10
M1-polarized macrophage-derived cellular nanovesicle-coated lipid nanoparticles for enhanced cancer treatment through hybridization of gene therapy and cancer immunotherapy.M1极化巨噬细胞衍生的细胞纳米囊泡包被的脂质纳米颗粒,通过基因治疗与癌症免疫治疗的杂交增强癌症治疗效果。
Acta Pharm Sin B. 2024 Jul;14(7):3169-3183. doi: 10.1016/j.apsb.2024.03.004. Epub 2024 Mar 7.
用于癌症免疫治疗的嵌合抗原受体自然杀伤细胞:从实验台到临床应用
Biomark Res. 2022 Mar 18;10(1):12. doi: 10.1186/s40364-022-00364-6.
4
Induced CAR-T Cell for the Potential Breakthrough to Overcome the Barriers of Current CAR-T Cell Therapy.诱导性嵌合抗原受体T细胞有望取得突破,克服当前嵌合抗原受体T细胞疗法的障碍。
Front Oncol. 2022 Feb 10;12:809754. doi: 10.3389/fonc.2022.809754. eCollection 2022.
5
CAR-macrophage: An extensive immune enhancer to fight cancer.嵌合抗原受体巨噬细胞:对抗癌症的强效免疫增强剂。
EBioMedicine. 2022 Feb;76:103873. doi: 10.1016/j.ebiom.2022.103873. Epub 2022 Feb 10.
6
In Vitro Engineering Chimeric Antigen Receptor Macrophages and T Cells by Lipid Nanoparticle-Mediated mRNA Delivery.通过脂质纳米颗粒介导的 mRNA 递送在体外工程嵌合抗原受体巨噬细胞和 T 细胞。
ACS Biomater Sci Eng. 2022 Feb 14;8(2):722-733. doi: 10.1021/acsbiomaterials.1c01532. Epub 2022 Feb 1.
7
FDA Approval Summary: Idecabtagene Vicleucel for Relapsed or Refractory Multiple Myeloma.FDA 批准概要:依达卡替(Idecabtagene Vicleucel)治疗复发/难治性多发性骨髓瘤。
Clin Cancer Res. 2022 May 2;28(9):1759-1764. doi: 10.1158/1078-0432.CCR-21-3803.
8
CAR T cells produced in vivo to treat cardiac injury.体内生成的 CAR T 细胞治疗心脏损伤。
Science. 2022 Jan 7;375(6576):91-96. doi: 10.1126/science.abm0594. Epub 2022 Jan 6.
9
Immune cell targeting nanoparticles: a review.免疫细胞靶向纳米颗粒:综述
Biomater Res. 2021 Dec 20;25(1):44. doi: 10.1186/s40824-021-00246-2.
10
An ionizable lipid toolbox for RNA delivery.用于 RNA 递送的可离子化脂质工具包。
Nat Commun. 2021 Dec 13;12(1):7233. doi: 10.1038/s41467-021-27493-0.