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纳米颗粒与 CAR-T 细胞治疗整合应用的挑战与进展:文献计量学分析

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

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

PubMed 2025/06/17(内容时间) Hum Vaccin Immunother Q2 · IF 4.2(JCR 2025)

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中文摘要

近年来,纳米颗粒与CAR-T 细胞疗法的整合发展迅速,受到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仍缺乏全面分析。为填补这一空白,我们对2013年至2024年Web of Science核心合集中收录的515篇文献进行了文献计量学分析。使用VOSviewer、CiteSpace和R-bibliometrix,我们分析了发文趋势、有影响力的期刊、国家和机构贡献、主要作者以及高影响力参考文献。在VOSviewer中进行了关键词共现分析,应用最小出现次数阈值为5。使用CiteSpace以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研究热点,尤其是CAR-T 细胞生产过程的优化以及克服免疫抑制性肿瘤微环境内障碍的策略。展望未来,研究预计将日益聚焦于脂质纳米颗粒、精准细胞追踪和siRNA递送平台等纳米技术。这些创新在提高CAR-T 疗法疗效方面具有巨大前景,尤其是在传统方法仍显不足的实体瘤治疗中。通过识别新兴方向和有影响力的研究趋势,我们的分析凸显了纳米颗粒与CAR-T 疗法之间的动态协同作用,有助于推动肿瘤免疫治疗的突破性进展。

本研究提供了数据驱动的见解,为临床试验设计提供依据,促进跨学科合作,并展示了该领域改变未来癌症治疗模式的强大潜力。

展开英文摘要原文

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.

论文信息

作者
Gao Y、Zhou Y、He X、Lin H、Fang K、Hou Q、Wang H、Zhang H
单位
Department of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China.China
文献类型
非美国政府资助研究
期刊
Human vaccines & immunotherapeutics2025 Dec
原文标识
PubMed 40527861 · DOI 10.1080/21645515.2025.2518634