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2010 年至 2022 年嵌合抗原受体(CAR)自然杀伤(NK)细胞相关研究的文献计量学和科学知识图谱研究。

A bibliometric and scientific knowledge-map study of the chimeric antigen receptor (CAR) natural killer (NK) cell-related research from 2010 to 2022.

机构信息

Senior Department of Hematology, the Fifth Medical Center of PLA General Hospital, Beijing, China.

Chinese PLA Medical School Beijing, Beijing, China.

出版信息

Front Immunol. 2022 Aug 12;13:969196. doi: 10.3389/fimmu.2022.969196. eCollection 2022.

DOI:10.3389/fimmu.2022.969196
PMID:36032149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9413055/
Abstract

OBJECTIVES

As emerging adoptive immunotherapy after CAR-T cell therapy, CAR-NK cell therapy has been developing rapidly in recent years. Presently, the research on CAR-NK cells has become a hotspot in the field of tumor immunotherapy.

METHODS

In this descriptive study, CtieSpace and VOSviewer were used to perform the bibliometric and scientific knowledge-map analysis of articles and reviews related to CAR-NK cells.

RESULTS

5371 authors from 715 institutions in 65 countries published 1028 papers about CAR-NK cells in 346 journals. The number of publications related to CAR-NK cells was increasing overall, especially from 2018 to 2021. The United States was in a leading position. The most active institution was Univ Texas, MD Anderson Cancer Center (USA). The journal with the most publications was , and the most co-cited journal was . The researcher with the most published papers was Winfried S. Wels, while the most co-cited researcher was Shannon L Maude. The research of CAR-NK cells in hematological malignancies and solid tumors (especially the selection of targets and the evaluation of efficacy and safety) was a research hotspot in this field. The emerging topics mainly included three aspects. First, further improve the proliferation and persistence of NK cells . Secondly, optimizing and improving the CAR structure for NK cells to improve the anti-tumor ability of CAR-NK cells. Thirdly, the related research of CRISPR/Cas9 gene-editing technology in constructing engineered immune cells.

CONCLUSION

In this study, a bibliometric and scientific knowledge-map study provided a unique and objective perspective for the CAR-NK cell field. This information would provide a helpful reference for researchers interested in this field.

摘要

目的

作为 CAR-T 细胞治疗后的新兴过继免疫疗法,CAR-NK 细胞治疗近年来发展迅速。目前,CAR-NK 细胞的研究已成为肿瘤免疫治疗领域的热点。

方法

本研究采用 Citespace 和 VOSviewer 对 CAR-NK 细胞相关的文章和综述进行文献计量学和科学知识图谱分析。

结果

来自 715 家机构的 5371 位作者在 346 种期刊上发表了 1028 篇关于 CAR-NK 细胞的论文。总体而言,与 CAR-NK 细胞相关的出版物数量呈增长趋势,尤其是 2018 年至 2021 年。美国处于领先地位,最活跃的机构是美国德克萨斯大学 MD 安德森癌症中心。发表论文最多的期刊是《自然评论免疫学》,被引频次最高的期刊是《柳叶刀肿瘤学》。发表论文最多的研究人员是 Winfried S. Wels,被引频次最高的研究人员是 Shannon L. Maude。CAR-NK 细胞在血液恶性肿瘤和实体瘤(尤其是靶点选择和疗效及安全性评价)的研究是该领域的研究热点。新兴主题主要包括三个方面:第一,进一步提高 NK 细胞的增殖和持久性;第二,优化和改进 CAR 结构,提高 CAR-NK 细胞的抗肿瘤能力;第三,CRISPR/Cas9 基因编辑技术在构建工程免疫细胞方面的相关研究。

结论

本研究通过文献计量学和科学知识图谱分析,为 CAR-NK 细胞领域提供了独特而客观的视角。这些信息将为该领域的研究人员提供有益的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/910517aa78b2/fimmu-13-969196-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/c5f78ed2f320/fimmu-13-969196-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/ec271182744d/fimmu-13-969196-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/66bfbdd5e4f0/fimmu-13-969196-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/fc1835f48775/fimmu-13-969196-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/3c1631c520ef/fimmu-13-969196-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/0fa71954682b/fimmu-13-969196-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/ddbb8dfc1cbe/fimmu-13-969196-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/910517aa78b2/fimmu-13-969196-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/c5f78ed2f320/fimmu-13-969196-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/ec271182744d/fimmu-13-969196-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/66bfbdd5e4f0/fimmu-13-969196-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/fc1835f48775/fimmu-13-969196-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/3c1631c520ef/fimmu-13-969196-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/0fa71954682b/fimmu-13-969196-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/ddbb8dfc1cbe/fimmu-13-969196-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2543/9413055/910517aa78b2/fimmu-13-969196-g008.jpg

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