B:肿瘤性T滤泡辅助细胞(TFH)串联在结节性TFH细胞淋巴瘤病理生物学中的作用。

IF 5.1 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Tania P. Sainz , Vishal Sahu , Javier A. Gomez , Nicholas J. Dcunha , Akshay V. Basi , Claudia Kettlun , Iman Sarami , Jared K. Burks , Deepa Sampath , Francisco Vega
{"title":"B:肿瘤性T滤泡辅助细胞(TFH)串联在结节性TFH细胞淋巴瘤病理生物学中的作用。","authors":"Tania P. Sainz ,&nbsp;Vishal Sahu ,&nbsp;Javier A. Gomez ,&nbsp;Nicholas J. Dcunha ,&nbsp;Akshay V. Basi ,&nbsp;Claudia Kettlun ,&nbsp;Iman Sarami ,&nbsp;Jared K. Burks ,&nbsp;Deepa Sampath ,&nbsp;Francisco Vega","doi":"10.1016/j.labinv.2024.102147","DOIUrl":null,"url":null,"abstract":"<div><div>Angioimmunoblastic T-cell lymphoma (AITL), the most common form of peripheral T-cell lymphoma, originates from follicular helper T (Tfh) cells and is notably resistant to current treatments. The disease progression and maintenance, at least in early stages, are driven by a complex interplay between neoplastic Tfh and clusters of B-cells within the tumor microenvironment, mirroring the functional crosstalk observed inside germinal centers. This interaction is further complicated by recurrent mutations, such as <em>TET2</em> and <em>DNMT3A</em>, which are present in both Tfh cells and B-cells. These findings suggest that the symbiotic relationship between these 2 cell types could represent a therapeutic vulnerability. This review examines the key components and signaling mechanisms involved in the synapses between B-cells and Tfh cells, emphasizing their significant role in the pathobiology of AITL and potential as therapeutic targets.</div></div>","PeriodicalId":17930,"journal":{"name":"Laboratory Investigation","volume":"104 11","pages":"Article 102147"},"PeriodicalIF":5.1000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Role of the Crosstalk B:Neoplastic T Follicular Helper Cells in the Pathobiology of Nodal T Follicular Helper Cell Lymphomas\",\"authors\":\"Tania P. Sainz ,&nbsp;Vishal Sahu ,&nbsp;Javier A. Gomez ,&nbsp;Nicholas J. Dcunha ,&nbsp;Akshay V. Basi ,&nbsp;Claudia Kettlun ,&nbsp;Iman Sarami ,&nbsp;Jared K. Burks ,&nbsp;Deepa Sampath ,&nbsp;Francisco Vega\",\"doi\":\"10.1016/j.labinv.2024.102147\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Angioimmunoblastic T-cell lymphoma (AITL), the most common form of peripheral T-cell lymphoma, originates from follicular helper T (Tfh) cells and is notably resistant to current treatments. The disease progression and maintenance, at least in early stages, are driven by a complex interplay between neoplastic Tfh and clusters of B-cells within the tumor microenvironment, mirroring the functional crosstalk observed inside germinal centers. This interaction is further complicated by recurrent mutations, such as <em>TET2</em> and <em>DNMT3A</em>, which are present in both Tfh cells and B-cells. These findings suggest that the symbiotic relationship between these 2 cell types could represent a therapeutic vulnerability. This review examines the key components and signaling mechanisms involved in the synapses between B-cells and Tfh cells, emphasizing their significant role in the pathobiology of AITL and potential as therapeutic targets.</div></div>\",\"PeriodicalId\":17930,\"journal\":{\"name\":\"Laboratory Investigation\",\"volume\":\"104 11\",\"pages\":\"Article 102147\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laboratory Investigation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0023683724018257\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory Investigation","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0023683724018257","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

摘要

血管免疫母细胞T细胞淋巴瘤(AITL)是外周T细胞淋巴瘤中最常见的一种,起源于滤泡辅助T细胞(Tfh),对目前的治疗具有明显的抗药性。至少在早期阶段,疾病的发展和维持是由肿瘤微环境中的肿瘤Tfh和B细胞群之间复杂的相互作用所驱动的,这反映了在生殖中心内观察到的功能性串扰。Tfh细胞和B细胞都存在的TET2和DNMT3A等复发性突变使这种相互作用变得更加复杂。这些发现表明,这两种细胞类型之间的共生关系可能代表着一种治疗漏洞。本综述探讨了 B 细胞和 Tfh 细胞之间突触所涉及的关键成分和信号转导机制,强调了它们在 AITL 病理生物学中的重要作用以及作为治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of the Crosstalk B:Neoplastic T Follicular Helper Cells in the Pathobiology of Nodal T Follicular Helper Cell Lymphomas
Angioimmunoblastic T-cell lymphoma (AITL), the most common form of peripheral T-cell lymphoma, originates from follicular helper T (Tfh) cells and is notably resistant to current treatments. The disease progression and maintenance, at least in early stages, are driven by a complex interplay between neoplastic Tfh and clusters of B-cells within the tumor microenvironment, mirroring the functional crosstalk observed inside germinal centers. This interaction is further complicated by recurrent mutations, such as TET2 and DNMT3A, which are present in both Tfh cells and B-cells. These findings suggest that the symbiotic relationship between these 2 cell types could represent a therapeutic vulnerability. This review examines the key components and signaling mechanisms involved in the synapses between B-cells and Tfh cells, emphasizing their significant role in the pathobiology of AITL and potential as therapeutic targets.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Laboratory Investigation
Laboratory Investigation 医学-病理学
CiteScore
8.30
自引率
0.00%
发文量
125
审稿时长
2 months
期刊介绍: Laboratory Investigation is an international journal owned by the United States and Canadian Academy of Pathology. Laboratory Investigation offers prompt publication of high-quality original research in all biomedical disciplines relating to the understanding of human disease and the application of new methods to the diagnosis of disease. Both human and experimental studies are welcome.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信