{"title":"低剂量辐射下免疫反应的结构和时间动力学分析:历史、研究热点和新趋势。","authors":"Shu-Yuan Wang, Jia-Xing Wu, Xian An, Zhen Yuan, Yi-Fan Ren, Xiu-Feng Yu, Xiao-Dong Tian, Wei Wei","doi":"10.4329/wjr.v17.i4.101636","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Radiotherapy (RT) is a cornerstone of cancer treatment. Compared with conventional high-dose radiation, low-dose radiation (LDR) causes less damage to normal tissues while potentially modulating immune responses and inhibiting tumor growth. LDR stimulates both innate and adaptive immunity, enhancing the activity of natural killer cells, dendritic cells, and T cells. However, the mechanisms underlying the effects of LDR on the immune system remain unclear.</p><p><strong>Aim: </strong>To explore the history, research hotspots, and emerging trends in immune response to LDR literature over the past two decades.</p><p><strong>Methods: </strong>Publications on immune responses to LDR were retrieved from the Web of Science Core Collection. Bibliometric tools, including CiteSpace and HistCite, were used to identify historical features, active topics, and emerging trends in this field.</p><p><strong>Results: </strong>Analysis of 1244 publications over the past two decades revealed a significant surge in research on immune responses to LDR, particularly in the last decade. Key journals such as <i>INR J Radiat Biol</i>, <i>Cancers</i>, and <i>Radiat Res</i> published pivotal studies. Citation networks identified key studies by authors like Twyman-Saint Victor C (2015) and Vanpouille-Box C (2017). Keyword analysis revealed hotspots such as ipilimumab, stereotactic body RT, and targeted therapy, possibly identifying future research directions. Temporal variations in keyword clusters and alluvial flow maps illustrate the evolution of research themes over time.</p><p><strong>Conclusion: </strong>This bibliometric analysis provides valuable insights into the evolution of studies on responses to LDR, highlights research trends, and identifies emerging areas for further investigation.</p>","PeriodicalId":23819,"journal":{"name":"World journal of radiology","volume":"17 4","pages":"101636"},"PeriodicalIF":1.4000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12038408/pdf/","citationCount":"0","resultStr":"{\"title\":\"Structural and temporal dynamics analysis on immune response in low-dose radiation: History, research hotspots and emerging trends.\",\"authors\":\"Shu-Yuan Wang, Jia-Xing Wu, Xian An, Zhen Yuan, Yi-Fan Ren, Xiu-Feng Yu, Xiao-Dong Tian, Wei Wei\",\"doi\":\"10.4329/wjr.v17.i4.101636\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Radiotherapy (RT) is a cornerstone of cancer treatment. Compared with conventional high-dose radiation, low-dose radiation (LDR) causes less damage to normal tissues while potentially modulating immune responses and inhibiting tumor growth. LDR stimulates both innate and adaptive immunity, enhancing the activity of natural killer cells, dendritic cells, and T cells. However, the mechanisms underlying the effects of LDR on the immune system remain unclear.</p><p><strong>Aim: </strong>To explore the history, research hotspots, and emerging trends in immune response to LDR literature over the past two decades.</p><p><strong>Methods: </strong>Publications on immune responses to LDR were retrieved from the Web of Science Core Collection. Bibliometric tools, including CiteSpace and HistCite, were used to identify historical features, active topics, and emerging trends in this field.</p><p><strong>Results: </strong>Analysis of 1244 publications over the past two decades revealed a significant surge in research on immune responses to LDR, particularly in the last decade. Key journals such as <i>INR J Radiat Biol</i>, <i>Cancers</i>, and <i>Radiat Res</i> published pivotal studies. Citation networks identified key studies by authors like Twyman-Saint Victor C (2015) and Vanpouille-Box C (2017). Keyword analysis revealed hotspots such as ipilimumab, stereotactic body RT, and targeted therapy, possibly identifying future research directions. Temporal variations in keyword clusters and alluvial flow maps illustrate the evolution of research themes over time.</p><p><strong>Conclusion: </strong>This bibliometric analysis provides valuable insights into the evolution of studies on responses to LDR, highlights research trends, and identifies emerging areas for further investigation.</p>\",\"PeriodicalId\":23819,\"journal\":{\"name\":\"World journal of radiology\",\"volume\":\"17 4\",\"pages\":\"101636\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12038408/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World journal of radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4329/wjr.v17.i4.101636\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4329/wjr.v17.i4.101636","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0
摘要
背景:放疗(RT)是癌症治疗的基石。与传统的高剂量辐射相比,低剂量辐射(LDR)对正常组织的损伤较小,同时可能调节免疫反应并抑制肿瘤生长。LDR刺激先天免疫和适应性免疫,增强自然杀伤细胞、树突状细胞和T细胞的活性。然而,LDR对免疫系统影响的机制尚不清楚。目的:探讨近二十年来LDR免疫应答研究的历史、研究热点和新趋势。方法:从Web of Science Core Collection中检索有关LDR免疫应答的出版物。文献计量工具,包括CiteSpace和HistCite,被用来识别该领域的历史特征、活跃主题和新兴趋势。结果:对过去二十年中1244篇出版物的分析显示,特别是在过去十年中,对LDR免疫反应的研究显着激增。INR J Radiat Biol、cancer和Radiat Res等关键期刊发表了关键研究。引文网络确定了Twyman-Saint Victor C(2015)和Vanpouille-Box C(2017)等作者的关键研究。关键词分析揭示了易普利姆单抗、立体定向体RT、靶向治疗等热点,可能为未来的研究方向指明方向。关键词集群和冲积流图的时间变化说明了研究主题随时间的演变。结论:这一文献计量学分析为LDR响应研究的演变提供了有价值的见解,突出了研究趋势,并确定了进一步研究的新兴领域。
Structural and temporal dynamics analysis on immune response in low-dose radiation: History, research hotspots and emerging trends.
Background: Radiotherapy (RT) is a cornerstone of cancer treatment. Compared with conventional high-dose radiation, low-dose radiation (LDR) causes less damage to normal tissues while potentially modulating immune responses and inhibiting tumor growth. LDR stimulates both innate and adaptive immunity, enhancing the activity of natural killer cells, dendritic cells, and T cells. However, the mechanisms underlying the effects of LDR on the immune system remain unclear.
Aim: To explore the history, research hotspots, and emerging trends in immune response to LDR literature over the past two decades.
Methods: Publications on immune responses to LDR were retrieved from the Web of Science Core Collection. Bibliometric tools, including CiteSpace and HistCite, were used to identify historical features, active topics, and emerging trends in this field.
Results: Analysis of 1244 publications over the past two decades revealed a significant surge in research on immune responses to LDR, particularly in the last decade. Key journals such as INR J Radiat Biol, Cancers, and Radiat Res published pivotal studies. Citation networks identified key studies by authors like Twyman-Saint Victor C (2015) and Vanpouille-Box C (2017). Keyword analysis revealed hotspots such as ipilimumab, stereotactic body RT, and targeted therapy, possibly identifying future research directions. Temporal variations in keyword clusters and alluvial flow maps illustrate the evolution of research themes over time.
Conclusion: This bibliometric analysis provides valuable insights into the evolution of studies on responses to LDR, highlights research trends, and identifies emerging areas for further investigation.