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Purpose To explore the feasibility of a new technetium 99m-labeled nanobody (Tc-antifibroblast activation protein nanobody [AFN]) with high affinity to fibroblast activation protein for noninvasive monitoring of fibroblast activation after myocardial infarction. Materials and Methods Tc-AFN was prepared by site-specific labeling. Dynamic SPECT/CT imaging from 0.5 to 4 hours after injection of Tc-AFN was performed in male C57/BL6 mice at 8 weeks of age with the ischemia-reperfusion (IR) injury on day 7 ( = 4). Furthermore, IR mice underwent Tc-AFN SPECT/CT imaging on postoperative days 3, 7, 14, and 28 at 1 hour following injection. Ex vivo SPECT/CT imaging, blocking imaging, and biodistribution studies were performed on day 7 and compared with a Tc-labeled fibroblast activation protein inhibitor (FAPI)-04-derived radiotracer (Tc-HFAPi). Preclinical evaluation of Tc-AFN in a swine model of myocardial infarction was performed on day 7. Biodistributions and quantitative results were compared between groups using analysis of variance and tests. Results The accumulation of Tc-AFN at the infarcted region was most clearly visible at 1 hour following injection. Tc-AFN uptake on SPECT/CT images in the infarcted myocardium was visible from day 3, and maximum uptake occurred on day 7. At 1 hour after injection, the Tc-AFN and Tc-HFAPi uptake ratios (means ± SDs) were 2.23 ± 0.82 versus 1.34 ± 0.21 ( = .05), respectively, for infarcted to noninfarcted regions and 1.08 ± 0.49 versus 0.89 ± 0.42 ( = .34) for infarcted region to blood, respectively. Immunohistochemical examinations confirmed that maximum myocardium fibrosis and FAP expression was observed on day 7. Tc-AFN uptake in the infarcted myocardium was also clearly visualized with the swine model of myocardial infarction. Conclusion This study demonstrated the potential of Tc-AFN for noninvasive monitoring of fibroblast activation after myocardial infarction, which may be a new option for clinical imaging. Fibroblast Activation Protein, Nanobody, Tc-AFN, Tc-HFAPi, Myocardial Infarction © RSNA, 2025.
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http://dx.doi.org/10.1148/ryct.240204 | DOI Listing |
J Appl Microbiol
September 2025
Sivas Cumhuriyet University, Faculty of Medicine, Department of Medical Microbiology, 58140 Sivas, Türkiye.
Aims: The increasing antimicrobial resistance, particularly in Acinetobacter baumannii, complicates the treatment of infections, leading to higher morbidity, mortality, and economic costs. Herein, we aimed to determine the in vitro antimicrobial, synergistic, and antibiofilm activities of colistin (COL), meropenem, and ciprofloxacin antibiotics, and curcumin, punicalagin, geraniol (GER), and linalool (LIN) plant-active ingredients alone and in combination against 31 multidrug-resistant (MDR) A. baumannii clinical isolates.
View Article and Find Full Text PDFNan Fang Yi Ke Da Xue Xue Bao
August 2025
Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, China.
Objectives: To investigate the effect of (HP) on bleomycin (BLM)-induced pulmonary fibrosis in mice and on TGF-β1-induced human fetal lung fibroblasts (HFL1).
Methods: Thirty male C57BL/6 mice were randomly divided into control group, BLM-induced pulmonary fibrosis model group, low- and high-dose HP treatment groups (3 and 21 mg/kg, respectively), and 300 mg/kg pirfenidone (positive control) group. The effects of drug treatment for 21 days were assessed by examining respiratory function, lung histopathology, and expression of fibrosis markers in the lung tissues of the mouse models.
Braz J Otorhinolaryngol
September 2025
Zhejiang University, College of Medicine, Department of Otolaryngology, Hangzhou City, Zhejiang Province, China.
Objectives: Exosomes play a crucial role in intercellular communication and may contribute to the development of various diseases. Nevertheless, their role in Nasal Polyps (NPs) remains poorly understood. Herein, Nasal Polyp Fibroblasts (NPF) were used to release exosomes, and epithelial cells were cocultured with NPF-derived exosomes to analyze Epithelial-Mesenchymal Transition (EMT) in Chronic Rhinosinusitis (CRS).
View Article and Find Full Text PDFClin Nucl Med
September 2025
Women Health Program, Sultan Qaboos Comprehensive Cancer Care and Research Centre (SQCCCRC), University Medical City, Muscat, Oman.
We report the case of a 47-year-old woman who presented with left inguinal swelling; the biopsy of which showed high-grade serous adenocarcinoma. 68Ga-FAPI PET/CT revealed a tracer-avid lesion in the left adnexal region and an enlarged left inguinal nodal mass (site of biopsy). Multiple focal lesions were also seen at the hepatic dome, along the falciform ligament and at the right lateral abdominal wall, suspicious for peritoneal/metastatic deposits.
View Article and Find Full Text PDFAnn Rheum Dis
September 2025
Department of Pediatrics, Division of Rheumatology, University of Michigan, Ann Arbor, MI, USA.
Objectives: Juvenile dermatomyositis (JDM) is a heterogeneous autoimmune condition needing targeted treatment approaches and improved understanding of molecular mechanisms driving clinical phenotypes. We utilised exploratory proteomics from a longitudinal North American cohort of patients with new-onset JDM to identify biological pathways at disease onset and follow-up, tissue-specific disease activity, and myositis-specific autoantibody (MSA) status.
Methods: We measured 3072 plasma proteins (Olink panel) in 56 patients with JDM within 12 weeks of starting treatment (from the Childhood Arthritis and Rheumatology Research Alliance Registry and 3 additional sites) and 8 paediatric controls.