Fibroblast activation protein inhibitor PET/CT as an emerging diagnostic modality in interstitial lung disease and other fibrotic conditions.

Rheumatology and immunology research Pub Date : 2024-10-21 eCollection Date: 2024-09-01 DOI:10.2478/rir-2024-0021
Mihai Tudor Albu, Alexandru-Emil Matei, Jörg H W Distler, Frederik L Giesel, Yuriko Mori
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Abstract

Interstitial lung diseases (ILD) encompass a wide range of disorders characterized by alveolar inflammation and fibrotic tissue remodeling, marked by significant morbidity and mortality. Systemic sclerosis (SSc), among other connective tissue diseases, is a frequent cause of ILD. Assessment of pulmonary fibrosis is frequently constrained by the delayed manifestations of profibrotic activation of fibroblasts, which results in late macroscopic alterations detectable by standard imaging techniques such as computed tomography (CT) and magnetic resonance imaging (MRI) scans. 68Ga-labeled fibroblast activation protein inhibitors (68Ga-FAPI [fibroblast activation protein inhibitor]) are novel radionuclides used in the selective positron emission tomography/computed tomography (PET/CT) detection of profibrotic fibroblasts, a key player in fibrotic tissue remodeling. Application of 68Ga-FAPI in different target organs undergoing fibrosis, such as lung and heart, highlights its efficacy in detecting ongoing fibrotic processes, since FAPI tracer uptake has been correlated with clinical disease progression markers in SSc-ILD. This feature could enable physicians to detect subclinical fibrotic activity and tailor an individualised therapy plan on a case by case basis. The use of 68Ga-FAPI in ILD and other fibrotic conditions may emerge as a novel tool in future clinical practice for both activity monitoring and treatment optimisation. Other tracers tested in ILD of different etiologies have shown promising results and may in future also be considered for potential application in SSc-ILD.

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成纤维细胞活化蛋白抑制剂 PET/CT 作为间质性肺病和其他纤维化病症的一种新兴诊断方式。
间质性肺疾病(ILD)包括一系列以肺泡炎症和纤维组织重塑为特征的疾病,发病率和死亡率都很高。除其他结缔组织疾病外,系统性硬化症(SSc)也是导致 ILD 的常见原因。对肺纤维化的评估经常受到成纤维细胞凋亡性激活的延迟表现的限制,这导致计算机断层扫描(CT)和磁共振成像(MRI)扫描等标准成像技术无法检测到晚期的宏观改变。68Ga 标记的成纤维细胞活化蛋白抑制剂(68Ga-FAPI[成纤维细胞活化蛋白抑制剂])是一种新型放射性核素,可用于选择性正电子发射断层扫描/计算机断层扫描(PET/CT)检测纤维化组织重塑过程中起关键作用的异型成纤维细胞。68Ga-FAPI 在肺部和心脏等不同纤维化靶器官中的应用,凸显了它在检测持续纤维化过程中的功效,因为 FAPI 示踪剂摄取与 SSc-ILD 的临床疾病进展标志物相关。这一特性可帮助医生检测亚临床纤维化活动,并根据具体情况制定个体化治疗方案。在 ILD 和其他纤维化疾病中使用 68Ga-FAPI 可能会成为未来临床实践中监测活动和优化治疗的新工具。在不同病因的 ILD 中测试的其他示踪剂也显示出了良好的效果,将来也可能被考虑应用于 SSc-ILD 中。
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Blau syndrome mimics Takayasu's arteritis: Report of 2 cases with literature review. Extracellular vesicles and interstitial lung disease in systemic sclerosis: State of the art! Fibroblast activation protein inhibitor PET/CT as an emerging diagnostic modality in interstitial lung disease and other fibrotic conditions. High resolution computed tomography in systemic sclerosis: From diagnosis to follow-up. MIP-C: A new autoimmune rheumatic disease concomitant with the COVID-19 pandemic.
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