Albu Mihai Tudor, Matei Alexandru-Emil, Distler Jörg H W, Giesel Frederik L, Mori Yuriko
Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Hiller Research Center, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Rheumatol Immunol Res. 2024 Oct 21;5(3):152-156. doi: 10.2478/rir-2024-0021. eCollection 2024 Sep.
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.
间质性肺疾病(ILD)涵盖了多种以肺泡炎症和纤维化组织重塑为特征的疾病,其发病率和死亡率都很高。系统性硬化症(SSc)是结缔组织疾病中导致ILD的常见病因。肺纤维化的评估常常受到成纤维细胞促纤维化激活延迟表现的限制,这导致标准成像技术(如计算机断层扫描(CT)和磁共振成像(MRI)扫描)检测到的宏观改变较晚出现。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)检测促纤维化成纤维细胞的新型放射性核素,促纤维化成纤维细胞是纤维化组织重塑的关键因素。68Ga-FAPI在不同的纤维化靶器官(如肺和心脏)中的应用突出了其在检测正在进行的纤维化过程中的功效,因为FAPI示踪剂摄取与SSc-ILD中的临床疾病进展标志物相关。这一特性可以使医生检测亚临床纤维化活动,并根据具体情况制定个性化的治疗方案。68Ga-FAPI在ILD和其他纤维化疾病中的应用可能会成为未来临床实践中用于活动监测和治疗优化的一种新型工具。在不同病因的ILD中测试的其他示踪剂也显示出了有前景的结果,未来也可能会考虑将其应用于SSc-ILD。