• 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

生物材料促进 CAR-T 细胞的生成和免疫治疗。

Biomaterials promote generation and immunotherapy of CAR-T cells.

机构信息

College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.

ZJU-Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, China.

出版信息

Front Immunol. 2023 Apr 20;14:1165576. doi: 10.3389/fimmu.2023.1165576. eCollection 2023.

DOI:10.3389/fimmu.2023.1165576
PMID:37153571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10157406/
Abstract

Chimeric antigen receptor-T (CAR-T) cell therapy based on functional immune cell transfer is showing a booming situation. However, complex manufacturing processes, high costs, and disappointing results in the treatment of solid tumors have limited its use. Encouragingly, it has facilitated the development of new strategies that fuse immunology, cell biology, and biomaterials to overcome these obstacles. In recent years, CAR-T engineering assisted by properly designed biomaterials has improved therapeutic efficacy and reduced side effects, providing a sustainable strategy for improving cancer immunotherapy. At the same time, the low cost and diversity of biomaterials also offer the possibility of industrial production and commercialization. Here, we summarize the role of biomaterials as gene delivery vehicles in the generation of CAR-T cells and highlight the advantages of construction . Then, we focused on how biomaterials can be combined with CAR-T cells to better enable synergistic immunotherapy in the treatment of solid tumors. Finally, we describe biomaterials' potential challenges and prospects in CAR-T therapy. This review aims to provide a detailed overview of biomaterial-based CAR-T tumor immunotherapy to help investigators reference and customize biomaterials for CAR-T therapy to improve the efficacy of immunotherapy.

摘要

嵌合抗原受体-T(CAR-T)细胞疗法基于功能性免疫细胞的转移,呈现出蓬勃发展的态势。然而,其在实体瘤治疗中复杂的制造工艺、高昂的成本和令人失望的结果限制了其应用。令人鼓舞的是,它促进了新策略的发展,这些策略将免疫学、细胞生物学和生物材料融合在一起,以克服这些障碍。近年来,通过适当设计的生物材料辅助的 CAR-T 工程提高了治疗效果,降低了副作用,为改善癌症免疫疗法提供了可持续的策略。同时,生物材料的低成本和多样性也为工业生产和商业化提供了可能性。在这里,我们总结了生物材料作为基因传递载体在 CAR-T 细胞生成中的作用,并强调了构建的优势。然后,我们重点讨论了生物材料如何与 CAR-T 细胞结合,以更好地实现协同免疫治疗,治疗实体瘤。最后,我们描述了生物材料在 CAR-T 治疗中的潜在挑战和前景。本综述旨在提供基于生物材料的 CAR-T 肿瘤免疫治疗的详细概述,以帮助研究人员参考和定制用于 CAR-T 治疗的生物材料,以提高免疫治疗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/50c897b01ec9/fimmu-14-1165576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/3d5009f48740/fimmu-14-1165576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/8fe91a52bf61/fimmu-14-1165576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/3fd41678c892/fimmu-14-1165576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/5137cd900906/fimmu-14-1165576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/9a3d735e7648/fimmu-14-1165576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/50c897b01ec9/fimmu-14-1165576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/3d5009f48740/fimmu-14-1165576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/8fe91a52bf61/fimmu-14-1165576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/3fd41678c892/fimmu-14-1165576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/5137cd900906/fimmu-14-1165576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/9a3d735e7648/fimmu-14-1165576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286c/10157406/50c897b01ec9/fimmu-14-1165576-g006.jpg

相似文献

1
Biomaterials promote generation and immunotherapy of CAR-T cells.生物材料促进 CAR-T 细胞的生成和免疫治疗。
Front Immunol. 2023 Apr 20;14:1165576. doi: 10.3389/fimmu.2023.1165576. eCollection 2023.
2
Biomaterials for chimeric antigen receptor T cell engineering.用于嵌合抗原受体 T 细胞工程的生物材料。
Acta Biomater. 2023 Aug;166:1-13. doi: 10.1016/j.actbio.2023.04.043. Epub 2023 May 2.
3
Biomaterials in Chimeric Antigen Receptor T-Cell Process Development.嵌合抗原受体T细胞工艺开发中的生物材料
Acc Chem Res. 2020 Sep 15;53(9):1724-1738. doi: 10.1021/acs.accounts.0c00335. Epub 2020 Aug 6.
4
Obstacles and Coping Strategies of CAR-T Cell Immunotherapy in Solid Tumors.实体瘤嵌合抗原受体 T 细胞免疫疗法的障碍和应对策略。
Front Immunol. 2021 May 19;12:687822. doi: 10.3389/fimmu.2021.687822. eCollection 2021.
5
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.
6
Recent advances in biomaterial designs for assisting CAR-T cell therapy towards potential solid tumor treatment.生物材料设计在辅助 CAR-T 细胞疗法治疗实体瘤方面的最新进展。
Nanoscale. 2024 Feb 15;16(7):3226-3242. doi: 10.1039/d3nr05768b.
7
Advanced Materials and Delivery Systems for Enhancement of Chimeric Antigen Receptor Cells.用于增强嵌合抗原受体细胞的先进材料与递送系统
Small Methods. 2023 Nov;7(11):e2300880. doi: 10.1002/smtd.202300880. Epub 2023 Aug 31.
8
Chimeric antigen receptor-engineered T-cell therapy for liver cancer.嵌合抗原受体修饰的 T 细胞治疗肝癌。
Hepatobiliary Pancreat Dis Int. 2018 Aug;17(4):301-309. doi: 10.1016/j.hbpd.2018.05.005. Epub 2018 May 24.
9
Synthetic Biology in Chimeric Antigen Receptor T (CAR T) Cell Engineering.合成生物学在嵌合抗原受体 T(CAR T)细胞工程中的应用。
ACS Synth Biol. 2022 Jan 21;11(1):1-15. doi: 10.1021/acssynbio.1c00256. Epub 2022 Jan 10.
10
Taking Lessons from CAR-T Cells and Going Beyond: Tailoring Design and Signaling for CAR-NK Cells in Cancer Therapy.从 CAR-T 细胞中汲取经验并超越:在癌症治疗中为 CAR-NK 细胞定制设计和信号传导。
Front Immunol. 2022 Mar 18;13:822298. doi: 10.3389/fimmu.2022.822298. eCollection 2022.

引用本文的文献

1
Research on the application of biomaterial-based responsive hydrogels in the tumor microenvironment.基于生物材料的响应性水凝胶在肿瘤微环境中的应用研究
PeerJ. 2025 Jul 8;13:e19609. doi: 10.7717/peerj.19609. eCollection 2025.
2
Nickel nanoparticles: a novel platform for cancer-targeted delivery and multimodal therapy.镍纳米颗粒:一种用于癌症靶向递送和多模态治疗的新型平台。
Front Drug Deliv. 2025 Jul 30;5:1627556. doi: 10.3389/fddev.2025.1627556. eCollection 2025.
3
Lung metastasis and recurrence is mitigated by CAR macrophages, in-situ-generated from mRNA delivered by small extracellular vesicles.

本文引用的文献

1
Therapeutic in vivo delivery of gene editing agents.基因编辑试剂的治疗性体内递送。
Cell. 2022 Jul 21;185(15):2806-2827. doi: 10.1016/j.cell.2022.03.045. Epub 2022 Jul 6.
2
Potentiating adoptive cell therapy using synthetic IL-9 receptors.利用合成的白细胞介素-9 受体增强过继细胞疗法。
Nature. 2022 Jul;607(7918):360-365. doi: 10.1038/s41586-022-04801-2. Epub 2022 Jun 8.
3
Nanotechnology-enabled immunoengineering approaches to advance therapeutic applications.采用纳米技术的免疫工程方法推动治疗应用。
由小细胞外囊泡递送的mRNA原位生成的CAR巨噬细胞可减轻肺转移和复发。
Nat Commun. 2025 Aug 4;16(1):7166. doi: 10.1038/s41467-025-62506-2.
4
Advancing CAR-based cell therapies for solid tumours: challenges, therapeutic strategies, and perspectives.推进基于嵌合抗原受体(CAR)的实体瘤细胞疗法:挑战、治疗策略及展望
Mol Cancer. 2025 Jul 7;24(1):191. doi: 10.1186/s12943-025-02386-8.
5
CAR-T cell therapy in brain malignancies: obstacles in the face of cellular trafficking and persistence.嵌合抗原受体T细胞疗法在脑恶性肿瘤中的应用:细胞转运与存活面临的障碍
Front Immunol. 2025 Jun 19;16:1596499. doi: 10.3389/fimmu.2025.1596499. eCollection 2025.
6
enhancement of CD8+ T cell activity using functionalized hydrogel encapsulating tonsil-derived lymphatic endothelial cells.使用包裹扁桃体来源的淋巴管内皮细胞的功能化水凝胶增强CD8 + T细胞活性。
Theranostics. 2025 Jan 1;15(3):850-874. doi: 10.7150/thno.100079. eCollection 2025.
7
From ex vivo to in vivo chimeric antigen T cells manufacturing: new horizons for CAR T-cell based therapy.从体外到体内嵌合抗原T细胞制造:基于CAR-T细胞疗法的新视野
J Transl Med. 2025 Jan 4;23(1):10. doi: 10.1186/s12967-024-06052-3.
8
Universal CAR cell therapy: Challenges and expanding applications.通用嵌合抗原受体(CAR)细胞疗法:挑战与应用拓展
Transl Oncol. 2025 Jan;51:102147. doi: 10.1016/j.tranon.2024.102147. Epub 2024 Oct 15.
9
Exploring the potential of the convergence between extracellular vesicles and CAR technology as a novel immunotherapy approach.探索细胞外囊泡与嵌合抗原受体(CAR)技术融合作为一种新型免疫治疗方法的潜力。
J Extracell Biol. 2024 Sep 26;3(9):e70011. doi: 10.1002/jex2.70011. eCollection 2024 Sep.
10
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.
Nano Converg. 2022 Apr 28;9(1):19. doi: 10.1186/s40580-022-00310-0.
4
Modulating tumor physical microenvironment for fueling CAR-T cell therapy.调节肿瘤物理微环境以增强 CAR-T 细胞疗法。
Adv Drug Deliv Rev. 2022 Jun;185:114301. doi: 10.1016/j.addr.2022.114301. Epub 2022 Apr 16.
5
Delivery of CAR-T cells in a transient injectable stimulatory hydrogel niche improves treatment of solid tumors.在瞬时可注射的刺激水凝胶龛内递送 CAR-T 细胞可改善实体瘤的治疗效果。
Sci Adv. 2022 Apr 8;8(14):eabn8264. doi: 10.1126/sciadv.abn8264.
6
Multifunctional theranostic nanoparticles for multi-modal imaging-guided CAR-T immunotherapy and chemo-photothermal combinational therapy of non-Hodgkin's lymphoma.多功能治疗性纳米粒子用于多模态成像引导的 CAR-T 免疫治疗和非霍奇金淋巴瘤的化疗-光热联合治疗。
Biomater Sci. 2022 May 17;10(10):2577-2589. doi: 10.1039/d1bm01982a.
7
Depletion of tumor associated macrophages enhances local and systemic platelet-mediated anti-PD-1 delivery for post-surgery tumor recurrence treatment.肿瘤相关巨噬细胞的消耗增强了局部和全身血小板介导的抗PD-1递送,用于术后肿瘤复发治疗。
Nat Commun. 2022 Apr 6;13(1):1845. doi: 10.1038/s41467-022-29388-0.
8
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.
9
Bioinstructive implantable scaffolds for rapid in vivo manufacture and release of CAR-T cells.用于快速体内制造和释放 CAR-T 细胞的生物指令性可植入支架。
Nat Biotechnol. 2022 Aug;40(8):1250-1258. doi: 10.1038/s41587-022-01245-x. Epub 2022 Mar 24.
10
Nanosensors in clinical development of CAR-T cell immunotherapy.嵌合抗原受体T细胞免疫疗法临床开发中的纳米传感器
Biosens Bioelectron. 2022 Jun 15;206:114124. doi: 10.1016/j.bios.2022.114124. Epub 2022 Mar 3.