Department of Nuclear Medicine, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
Department of Anatomy and Medical Imaging, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
J Med Radiat Sci. 2022 Dec;69(4):518-524. doi: 10.1002/jmrs.603. Epub 2022 Jun 27.
Tuberculosis (TB) lesions in humans have been proven to be severely hypoxic with hypoxia leading to latency and dormancy of disease. Dormant TB lesions become less susceptible to standard TB treatment regimens with varying responses to treatment but may have increased susceptibility to nitroimidazole drugs. This in turn implies that positron emission tomography / computed tomography (PET/CT) imaging with radiolabelled nitroimidazoles may identify patients who will benefit from treatment with antimicrobial agents that are active against anaerobic bacteria. This case series aims to highlight the hypoxic uptake and retention of a novel Ga-labelled hypoxia-seeking agent in TB lesions at different time points during anti-TB therapy using PET/CT imaging. Patients with confirmed TB underwent whole-body PET/CT after administration of a Ga-nitroimidazole derivative at baseline and follow-up. Images were analysed both qualitatively and semi-quantitatively. Hypoxic uptake and change in uptake over time were analysed using lesion-to-muscle ratio (LMR) and lesion-to-blood ratio (LBR). Ga-nitroimidazole avid lesions were demonstrated most frequently in the upper lobes of the lung. Low-grade hypoxic uptake was visualised in areas of consolidation, cavitation, nodules and lymph nodes. From baseline to follow-up imaging, the LMR increased with persistent hypoxic load despite morphologic improvement. This case series highlights the dynamic hypoxic microenvironment in TB lesions. From these initial data, it appears that Ga-nitroimidazole is a promising candidate for monitoring hypoxic load in patients diagnosed with TB. Such imaging could identify patients who would benefit from individualised therapy targeting other mechanisms in the TB microenvironment with the intention to predict or improve treatment response.
人类的结核病变已被证明严重缺氧,缺氧导致疾病的潜伏期和休眠期。休眠性结核病变对标准结核治疗方案的敏感性降低,对治疗的反应不一,但可能对硝基咪唑类药物的敏感性增加。这反过来意味着,用放射性标记的硝基咪唑类药物进行正电子发射断层扫描/计算机断层扫描(PET/CT)成像,可能可以识别出那些受益于针对厌氧菌的抗菌药物治疗的患者。本病例系列旨在强调使用 PET/CT 成像,在抗结核治疗的不同时间点,新型 Ga 标记的缺氧探针在结核病变中的缺氧摄取和保留情况。在给予 Ga 硝基咪唑衍生物后,对确诊为结核的患者进行全身 PET/CT 检查。对图像进行定性和半定量分析。使用病变肌肉比(LMR)和病变与血液比(LBR)分析缺氧摄取和随时间的摄取变化。 Ga 硝基咪唑探针在肺的上叶最常显示出高摄取。在实变、空洞、结节和淋巴结等区域可以观察到低水平的缺氧摄取。从基线到随访成像,尽管形态学改善,但 LMR 随着持续的缺氧负荷增加而增加。该病例系列强调了结核病变中的动态缺氧微环境。从这些初步数据来看,Ga 硝基咪唑似乎是监测诊断为结核的患者缺氧负荷的有前途的候选物。这种成像可以识别出那些受益于针对结核微环境中其他机制的个体化治疗的患者,以期预测或改善治疗反应。