Sixuan Cheng, Youzhuo Quan, Xingru Long, Xiaoli Lan, Dawei Jiang*, Kun Liu* and Cheng Fan*,
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PET imaging revealed significantly higher radioactivity concentration in inflamed joints compared to normal joints at all time points, with peak uptake of 11.73 %ID/g at 4 h postinjection compared to 1.55 %ID/g in noninflamed joints. Histological analysis confirmed the presence of T lymphocytes and macrophages in inflamed tissues and their high Kv1.3 expression. Additionally, tracer uptake correlated strongly with clinical arthritis scores (Pearson <i>r</i> = 0.8789, <i>p</i> < 0.0001), demonstrating the probe’s sensitivity in tracking arthritis progression. This study successfully developed a <sup>68</sup>Ga-labeled Kv1.3-targeting radiopharmaceutical that enables visualization of active inflammation in arthritic joints, showing high sensitivity for early RA diagnosis and disease monitoring. This approach offers potential for guiding immune-targeted therapies and assessing the treatment efficacy in RA.</p>","PeriodicalId":52,"journal":{"name":"Molecular Pharmaceutics","volume":"22 6","pages":"3447–3455 3447–3455"},"PeriodicalIF":4.5000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Detection of Voltage-Gated Potassium Channels 1.3 via Immuno-PET Visualizes Rheumatoid Arthritis\",\"authors\":\"Sixuan Cheng, Youzhuo Quan, Xingru Long, Xiaoli Lan, Dawei Jiang*, Kun Liu* and Cheng Fan*, \",\"doi\":\"10.1021/acs.molpharmaceut.5c0035710.1021/acs.molpharmaceut.5c00357\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Rheumatoid arthritis (RA) is a chronic inflammatory condition affecting approximately 1% of the global population, yet current diagnostic tools for early-stage RA lack sensitivity and fail to identify optimal treatment candidates. Voltage-gated potassium channel 1.3 (Kv1.3) plays a crucial role in immune cell activation, particularly in effector memory T lymphocytes and macrophages, which drive inflammation in active RA. This study aimed to develop and evaluate a novel Kv1.3-targeted radiopharmaceutical, [<sup>68</sup>Ga]Ga-NOTA-anti-Kv1.3, for precise monitoring and quantification of joint inflammation in a mouse model of RA. PET imaging revealed significantly higher radioactivity concentration in inflamed joints compared to normal joints at all time points, with peak uptake of 11.73 %ID/g at 4 h postinjection compared to 1.55 %ID/g in noninflamed joints. Histological analysis confirmed the presence of T lymphocytes and macrophages in inflamed tissues and their high Kv1.3 expression. Additionally, tracer uptake correlated strongly with clinical arthritis scores (Pearson <i>r</i> = 0.8789, <i>p</i> < 0.0001), demonstrating the probe’s sensitivity in tracking arthritis progression. This study successfully developed a <sup>68</sup>Ga-labeled Kv1.3-targeting radiopharmaceutical that enables visualization of active inflammation in arthritic joints, showing high sensitivity for early RA diagnosis and disease monitoring. This approach offers potential for guiding immune-targeted therapies and assessing the treatment efficacy in RA.</p>\",\"PeriodicalId\":52,\"journal\":{\"name\":\"Molecular Pharmaceutics\",\"volume\":\"22 6\",\"pages\":\"3447–3455 3447–3455\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-04-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Pharmaceutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.5c00357\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.5c00357","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
摘要
类风湿关节炎(RA)是一种影响全球约1%人口的慢性炎症性疾病,但目前用于早期RA的诊断工具缺乏敏感性,无法确定最佳的候选治疗方案。电压门控钾通道1.3 (Kv1.3)在免疫细胞激活中起着至关重要的作用,特别是在效应记忆T淋巴细胞和巨噬细胞中,它们在活动性RA中驱动炎症。本研究旨在开发和评估一种新的靶向kv1.3的放射性药物[68Ga]Ga-NOTA-anti-Kv1.3,用于精确监测和定量RA小鼠模型的关节炎症。PET成像显示,在所有时间点,炎症关节的放射性浓度明显高于正常关节,注射后4小时的峰值为11.73% ID/g,而非炎症关节的峰值为1.55% ID/g。组织学分析证实炎症组织中存在T淋巴细胞和巨噬细胞,且Kv1.3高表达。此外,示踪剂摄取与临床关节炎评分密切相关(Pearson r = 0.8789, p <;0.0001),证明了该探针在追踪关节炎进展方面的敏感性。本研究成功开发了一种68ga标记的kv1.3靶向放射性药物,能够可视化关节炎关节的活动性炎症,对RA的早期诊断和疾病监测具有很高的敏感性。该方法为指导免疫靶向治疗和评估RA的治疗效果提供了潜力。
Detection of Voltage-Gated Potassium Channels 1.3 via Immuno-PET Visualizes Rheumatoid Arthritis
Rheumatoid arthritis (RA) is a chronic inflammatory condition affecting approximately 1% of the global population, yet current diagnostic tools for early-stage RA lack sensitivity and fail to identify optimal treatment candidates. Voltage-gated potassium channel 1.3 (Kv1.3) plays a crucial role in immune cell activation, particularly in effector memory T lymphocytes and macrophages, which drive inflammation in active RA. This study aimed to develop and evaluate a novel Kv1.3-targeted radiopharmaceutical, [68Ga]Ga-NOTA-anti-Kv1.3, for precise monitoring and quantification of joint inflammation in a mouse model of RA. PET imaging revealed significantly higher radioactivity concentration in inflamed joints compared to normal joints at all time points, with peak uptake of 11.73 %ID/g at 4 h postinjection compared to 1.55 %ID/g in noninflamed joints. Histological analysis confirmed the presence of T lymphocytes and macrophages in inflamed tissues and their high Kv1.3 expression. Additionally, tracer uptake correlated strongly with clinical arthritis scores (Pearson r = 0.8789, p < 0.0001), demonstrating the probe’s sensitivity in tracking arthritis progression. This study successfully developed a 68Ga-labeled Kv1.3-targeting radiopharmaceutical that enables visualization of active inflammation in arthritic joints, showing high sensitivity for early RA diagnosis and disease monitoring. This approach offers potential for guiding immune-targeted therapies and assessing the treatment efficacy in RA.
期刊介绍:
Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development.
Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.