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纳米颗粒与嵌合抗原受体T细胞疗法联合应用的挑战与进展的文献计量分析

A bibliometric analysis of challenges and advancements in the integrated application of nanoparticles and chimeric antigen receptor T cell therapy.

作者信息

Gao Yang, Zhou Yang, He Xiaolin, Lin Hongwei, Fang Keying, Hou Qijun, Wang Huafang, Zhang Honghao, Zhang Yixi, Li Yuhua

机构信息

Department of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China.

Department of Anesthesiology, The Affiliated Nanhua Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, China.

出版信息

Hum Vaccin Immunother. 2025 Dec;21(1):2518634. doi: 10.1080/21645515.2025.2518634. Epub 2025 Jun 17.


DOI:10.1080/21645515.2025.2518634
PMID:40527861
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12184142/
Abstract

In recent years, the integration of nanoparticles with chimeric antigen receptor T-cell (CAR-T) therapy has advanced rapidly, garnering considerable attention from both academic and industrial sectors. However, a comprehensive analysis of key trends and emerging frontiers in this interdisciplinary field remains lacking. To address this gap, we conducted a bibliometric analysis of 515 publications indexed in the Web of Science Core Collection from 2013 to 2024. Using VOSviewer, CiteSpace, and R-bibliometrix, we analyzed publication trends, influential journals, national and institutional contributions, leading authors, and high-impact references. Keyword co-occurrence analyses were performed in VOSviewer, applying a minimum occurrence threshold of five. Citation bursts and clustering analyses of references and keywords were conducted using CiteSpace with default detection settings. Our analysis revealed major research hotspots, especially the optimization of CAR-T cell manufacturing processes and strategies to overcome barriers within the immunosuppressive tumor microenvironment. Looking forward, research is expected to focus increasingly on nanotechnologies such as lipid nanoparticles, precision cell tracking, and siRNA delivery platforms. These innovations hold substantial promise for enhancing the therapeutic efficacy of CAR-T therapies, particularly in the treatment of solid tumors, where conventional approaches remain inadequate. By identifying emerging directions and influential research trends, our analysis highlights the dynamic synergy between nanoparticles and CAR-T therapies, helping to fuel groundbreaking advances in tumor immunotherapy. This study provides data-driven insights that inform clinical trial design, foster interdisciplinary collaboration, and demonstrate the field's strong potential to transform future cancer treatment paradigms.

摘要

近年来,纳米颗粒与嵌合抗原受体T细胞(CAR-T)疗法的整合发展迅速,引起了学术界和工业界的广泛关注。然而,对这一跨学科领域的关键趋势和新兴前沿的全面分析仍然缺乏。为了填补这一空白,我们对2013年至2024年Web of Science核心合集中索引的515篇出版物进行了文献计量分析。我们使用VOSviewer、CiteSpace和R-bibliometrix分析了出版趋势、有影响力的期刊、国家和机构的贡献、主要作者以及高影响力参考文献。在VOSviewer中进行关键词共现分析,应用的最小出现阈值为五次。使用CiteSpace并采用默认检测设置对参考文献和关键词进行了引文爆发和聚类分析。我们的分析揭示了主要的研究热点,特别是CAR-T细胞制造工艺的优化以及克服免疫抑制肿瘤微环境中障碍的策略。展望未来,研究预计将越来越多地关注脂质纳米颗粒、精确细胞追踪和siRNA递送平台等纳米技术。这些创新对于提高CAR-T疗法的治疗效果具有巨大潜力,特别是在实体瘤治疗方面,传统方法仍然不足。通过识别新兴方向和有影响力的研究趋势,我们的分析突出了纳米颗粒与CAR-T疗法之间的动态协同作用,有助于推动肿瘤免疫治疗取得突破性进展。本研究提供了数据驱动的见解,为临床试验设计提供参考,促进跨学科合作,并展示了该领域在改变未来癌症治疗模式方面的强大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/af42c274b82a/KHVI_A_2518634_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/6a874eaf4a32/KHVI_A_2518634_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/9f4766912b73/KHVI_A_2518634_F0001_OC.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/775b9cafb5b4/KHVI_A_2518634_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/b59f8473f311/KHVI_A_2518634_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/5fbdfa5a8e19/KHVI_A_2518634_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/af42c274b82a/KHVI_A_2518634_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/6a874eaf4a32/KHVI_A_2518634_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/9f4766912b73/KHVI_A_2518634_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/1600fa092b08/KHVI_A_2518634_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/f8205da6fcff/KHVI_A_2518634_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/45a983d497eb/KHVI_A_2518634_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/775b9cafb5b4/KHVI_A_2518634_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/b59f8473f311/KHVI_A_2518634_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/5fbdfa5a8e19/KHVI_A_2518634_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df67/12184142/af42c274b82a/KHVI_A_2518634_F0008_OC.jpg

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本文引用的文献

[1]
Inhalable nanovesicles loaded with a STING agonist enhance CAR-T cell activity against solid tumors in the lung.

Nat Commun. 2025-1-2

[2]
Accelerating and optimising CAR T-cell manufacture to deliver better patient products.

Lancet Haematol. 2025-1

[3]
CAR T Cells and T-Cell Therapies for Cancer: A Translational Science Review.

JAMA. 2024-12-10

[4]
Biomimetic cell stimulation with a graphene oxide antigen-presenting platform for developing T cell-based therapies.

Nat Nanotechnol. 2024-12

[5]
In vivo CAR T cells move into clinical trials.

Nat Rev Drug Discov. 2024-10

[6]
Use of Respiratory Syncytial Virus Vaccines in Adults Aged ≥60 Years: Updated Recommendations of the Advisory Committee on Immunization Practices - United States, 2024.

MMWR Morb Mortal Wkly Rep. 2024-8-15

[7]
Recurrent Glioblastoma-Molecular Underpinnings and Evolving Treatment Paradigms.

Int J Mol Sci. 2024-6-19

[8]
Unlocking the Therapeutic Applicability of LNP-mRNA: Chemistry, Formulation, and Clinical Strategies.

Research (Wash D C). 2024-6-18

[9]
Subcutaneous biodegradable scaffolds for restimulating the antitumour activity of pre-administered CAR-T cells.

Nat Biomed Eng. 2025-2

[10]
Current understanding and management of CAR T cell-associated toxicities.

Nat Rev Clin Oncol. 2024-7

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