最近开发的用于细菌感染成像的放射性药物。

IF 4.4 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Maryke Kahts, Beverley Summers, Aadil Gutta, Wilfrid Pilloy, Thomas Ebenhan
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引用次数: 0

摘要

背景:尽管抗菌治疗取得了进步,对微生物的认识也有所提高,但感染仍然是发病和死亡的主要原因。抗菌药耐药性对全球构成重大威胁,快速准确地诊断感染和可靠地识别难治性感染对于有效治疗和应用抗生素管理变得越来越重要。利用核医学进行分子成像可以早期检测和定位感染和炎症过程,并准确监测治疗反应。人们一直在寻找更具特异性的放射性药物用于感染成像。本综述总结了自2019年以来,过去五年中在特异性细菌感染成像药物方面最突出的发现:本文报告了在患者研究中进行评估的一些前景广阔的新型放射性药物,包括放射性标记的细菌苷元(如[68Ga]Ga-DFO-B)、放射性标记的抗菌肽/肽片段(如[68Ga]Ga-NOTA-UBI29-41)以及针对细菌合成(如[68Ga]Ga-DFO-B)的药物、以及针对细菌合成途径(叶酸和肽聚糖)的制剂,如[11C]对氨基苯甲酸和 D-甲基-[11C]蛋氨酸,[18F]氟脱氧山梨醇以及 11C 和 18F 标记的三甲氧苄氨嘧啶的临床试验正在进行中。结论显然,在过去几年中,用于感染成像的新型放射性药物的研发工作付出了巨大努力,临床前研究也取得了显著进展。然而,将其转化为临床试验并最终应用于临床核医学实践的工作显然进展缓慢。作者认为,更有条理、更协调的临床前环境和精心设计的临床研究是可靠评估新提出的感染成像药物真正潜力的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recently developed radiopharmaceuticals for bacterial infection imaging

Background

Infection remains a major cause of morbidity and mortality, regardless of advances in antimicrobial therapy and improved knowledge of microorganisms. With the major global threat posed by antimicrobial resistance, fast and accurate diagnosis of infections, and the reliable identification of intractable infection, are becoming more crucial for effective treatment and the application of antibiotic stewardship. Molecular imaging with the use of nuclear medicine allows early detection and localisation of infection and inflammatory processes, as well as accurate monitoring of treatment response. There has been a continuous search for more specific radiopharmaceuticals to be utilised for infection imaging. This review summarises the most prominent discoveries in specifically bacterial infection imaging agents over the last five years, since 2019.

Main body

Some promising new radiopharmaceuticals evaluated in patient studies are reported here, including radiolabelled bacterial siderophores like [68Ga]Ga-DFO-B, radiolabelled antimicrobial peptide/peptide fragments like [68Ga]Ga-NOTA-UBI29-41, and agents that target bacterial synthesis pathways (folic acid and peptidoglycan) like [11C]para-aminobenzoic acid and D-methyl-[11C]-methionine, with clinical trials underway for [18F]fluorodeoxy-sorbitol, as well as for 11C- and 18F-labelled trimethoprim.

Conclusion

It is evident that a great deal of effort has gone into the development of new radiopharmaceuticals for infection imaging over the last few years, with remarkable progress in preclinical investigations. However, translation to clinical trials, and eventually clinical Nuclear Medicine practice, is apparently slow. It is the authors’ opinion that a more structured and harmonised preclinical setting and well-designed clinical investigations are the key to reliably evaluate the true potential of the newly proposed infection imaging agents.

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来源期刊
CiteScore
7.20
自引率
8.70%
发文量
30
审稿时长
5 weeks
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