Jinwei Qi, Junlin Chen, Saskia von Stillfried, Patrick Kozcera, Yang Shi, Anne Rix, Fabian Kiessling
{"title":"临床可翻译的crgd包被微泡分子超声成像评估炎症性肠病中αvβ3-整合素的表达","authors":"Jinwei Qi, Junlin Chen, Saskia von Stillfried, Patrick Kozcera, Yang Shi, Anne Rix, Fabian Kiessling","doi":"10.1097/RLI.0000000000001143","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Inflammatory bowel disease (IBD) subdivides into Crohn disease (CD) and ulcerative colitis (UC), and is characterized by unpredictable periods of inflammation and results in significant patient suffering and even death. Conventional diagnostic methods, for example, colonoscopy, computed tomography, or magnetic resonance imaging, have limitations such as invasiveness, patient discomfort, and limited sensitivity and accuracy. Therefore, we propose ultrasound molecular imaging (USMI) to detect and characterize IBD. First, we evaluated integrin-αvβ3 as a biomarker of IBD in human samples and then used clinically translatable cyclic Arg-Gly-Asp-D-Phe-Lys (cRGDfK)-coupled poly(butyl)cyanoacrylate microbubbles (cRGD-MB) to assess IBD in mice.</p><p><strong>Materials and methods: </strong>Vascular integrin-αvβ3 expression in human colon tissue samples (healthy, CD and UC, n = 10 per group) was analyzed by immunofluorescence staining. In mice, acute colitis was induced by administration of 4% dextran sodium sulfate in drinking water for 5 days. On day 7, USMI with cRGD-MB was performed in colitis (n = 6) and healthy (n = 5) mice. The signal of bound cRGD-MB was assessed by the destruction-replenishment method. Ex vivo analysis of mouse colon tissue was performed to assess the degree of colitis by hematoxylin-eosin staining and the vascular expression of integrin-αv by immunofluorescence.</p><p><strong>Results: </strong>Human samples showed a significantly higher vascular integrin-αvβ3 expression in CD and UC tissue, when compared with healthy samples (P < 0.005). In mice, a higher binding of cRGD-MB to inflamed colon was detected by USMI compared with healthy controls (P < 0.005). Immunofluorescence staining confirmed these findings, showing stronger integrin-αv expression in acute colitis, with a good correlation between USMI signal intensity and integrin-αv expression (r = 0.8, P = 0.0016).</p><p><strong>Conclusions: </strong>Integrin-αvβ3 on vessels is a suitable marker for IBD. USMI using cRGD-MB accurately detects this marker and correlates well with histology. These encouraging results support clinical translation of this imaging method as a noninvasive and cost-effective monitoring tool.</p>","PeriodicalId":14486,"journal":{"name":"Investigative Radiology","volume":" ","pages":""},"PeriodicalIF":7.0000,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular Ultrasound Imaging With Clinically Translatable cRGD-Coated Microbubbles to Assess αvβ3-Integrin Expression in Inflammatory Bowel Disease.\",\"authors\":\"Jinwei Qi, Junlin Chen, Saskia von Stillfried, Patrick Kozcera, Yang Shi, Anne Rix, Fabian Kiessling\",\"doi\":\"10.1097/RLI.0000000000001143\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Inflammatory bowel disease (IBD) subdivides into Crohn disease (CD) and ulcerative colitis (UC), and is characterized by unpredictable periods of inflammation and results in significant patient suffering and even death. Conventional diagnostic methods, for example, colonoscopy, computed tomography, or magnetic resonance imaging, have limitations such as invasiveness, patient discomfort, and limited sensitivity and accuracy. Therefore, we propose ultrasound molecular imaging (USMI) to detect and characterize IBD. First, we evaluated integrin-αvβ3 as a biomarker of IBD in human samples and then used clinically translatable cyclic Arg-Gly-Asp-D-Phe-Lys (cRGDfK)-coupled poly(butyl)cyanoacrylate microbubbles (cRGD-MB) to assess IBD in mice.</p><p><strong>Materials and methods: </strong>Vascular integrin-αvβ3 expression in human colon tissue samples (healthy, CD and UC, n = 10 per group) was analyzed by immunofluorescence staining. In mice, acute colitis was induced by administration of 4% dextran sodium sulfate in drinking water for 5 days. On day 7, USMI with cRGD-MB was performed in colitis (n = 6) and healthy (n = 5) mice. The signal of bound cRGD-MB was assessed by the destruction-replenishment method. Ex vivo analysis of mouse colon tissue was performed to assess the degree of colitis by hematoxylin-eosin staining and the vascular expression of integrin-αv by immunofluorescence.</p><p><strong>Results: </strong>Human samples showed a significantly higher vascular integrin-αvβ3 expression in CD and UC tissue, when compared with healthy samples (P < 0.005). In mice, a higher binding of cRGD-MB to inflamed colon was detected by USMI compared with healthy controls (P < 0.005). Immunofluorescence staining confirmed these findings, showing stronger integrin-αv expression in acute colitis, with a good correlation between USMI signal intensity and integrin-αv expression (r = 0.8, P = 0.0016).</p><p><strong>Conclusions: </strong>Integrin-αvβ3 on vessels is a suitable marker for IBD. USMI using cRGD-MB accurately detects this marker and correlates well with histology. 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引用次数: 0
摘要
目的:炎症性肠病(IBD)细分为克罗恩病(CD)和溃疡性结肠炎(UC),其特征是不可预测的炎症期,导致患者严重痛苦甚至死亡。传统的诊断方法,如结肠镜检查、计算机断层扫描或磁共振成像,都有局限性,如侵入性、患者不适、灵敏度和准确性有限。因此,我们提出超声分子成像(USMI)来检测和表征IBD。首先,我们评估了整合素-αvβ3作为人类IBD的生物标志物,然后使用临床可翻译的环arg - gy - asp - d - ph - lys (cRGDfK)偶联聚(丁基)氰丙烯酸酯微泡(cRGD-MB)来评估小鼠IBD。材料与方法:采用免疫荧光染色法分析血管整合素-αvβ3在人结肠组织(健康、CD和UC,每组n = 10)中的表达。小鼠在饮水中给予4%葡聚糖硫酸钠5天,诱导急性结肠炎。第7天,在结肠炎小鼠(n = 6)和健康小鼠(n = 5)中使用cRGD-MB进行USMI。结合的cRGD-MB信号通过破坏-补充法进行评估。体外分析小鼠结肠组织,苏木精-伊红染色评估结肠炎程度,免疫荧光检测血管中整合素-αv的表达。结果:人血管整合素-αvβ3在CD和UC组织中的表达明显高于健康组织(P < 0.005)。在小鼠中,USMI检测到cRGD-MB与炎症结肠的结合高于健康对照组(P < 0.005)。免疫荧光染色证实了这些发现,急性结肠炎中整合素-αv表达增强,USMI信号强度与整合素-αv表达有良好的相关性(r = 0.8, P = 0.0016)。结论:血管上的整合素-αvβ3是IBD的合适标志物。使用cRGD-MB的USMI可以准确地检测到该标记物,并且与组织学具有良好的相关性。这些令人鼓舞的结果支持这种成像方法作为一种无创和经济有效的监测工具的临床翻译。
Molecular Ultrasound Imaging With Clinically Translatable cRGD-Coated Microbubbles to Assess αvβ3-Integrin Expression in Inflammatory Bowel Disease.
Objectives: Inflammatory bowel disease (IBD) subdivides into Crohn disease (CD) and ulcerative colitis (UC), and is characterized by unpredictable periods of inflammation and results in significant patient suffering and even death. Conventional diagnostic methods, for example, colonoscopy, computed tomography, or magnetic resonance imaging, have limitations such as invasiveness, patient discomfort, and limited sensitivity and accuracy. Therefore, we propose ultrasound molecular imaging (USMI) to detect and characterize IBD. First, we evaluated integrin-αvβ3 as a biomarker of IBD in human samples and then used clinically translatable cyclic Arg-Gly-Asp-D-Phe-Lys (cRGDfK)-coupled poly(butyl)cyanoacrylate microbubbles (cRGD-MB) to assess IBD in mice.
Materials and methods: Vascular integrin-αvβ3 expression in human colon tissue samples (healthy, CD and UC, n = 10 per group) was analyzed by immunofluorescence staining. In mice, acute colitis was induced by administration of 4% dextran sodium sulfate in drinking water for 5 days. On day 7, USMI with cRGD-MB was performed in colitis (n = 6) and healthy (n = 5) mice. The signal of bound cRGD-MB was assessed by the destruction-replenishment method. Ex vivo analysis of mouse colon tissue was performed to assess the degree of colitis by hematoxylin-eosin staining and the vascular expression of integrin-αv by immunofluorescence.
Results: Human samples showed a significantly higher vascular integrin-αvβ3 expression in CD and UC tissue, when compared with healthy samples (P < 0.005). In mice, a higher binding of cRGD-MB to inflamed colon was detected by USMI compared with healthy controls (P < 0.005). Immunofluorescence staining confirmed these findings, showing stronger integrin-αv expression in acute colitis, with a good correlation between USMI signal intensity and integrin-αv expression (r = 0.8, P = 0.0016).
Conclusions: Integrin-αvβ3 on vessels is a suitable marker for IBD. USMI using cRGD-MB accurately detects this marker and correlates well with histology. These encouraging results support clinical translation of this imaging method as a noninvasive and cost-effective monitoring tool.
期刊介绍:
Investigative Radiology publishes original, peer-reviewed reports on clinical and laboratory investigations in diagnostic imaging, the diagnostic use of radioactive isotopes, computed tomography, positron emission tomography, magnetic resonance imaging, ultrasound, digital subtraction angiography, and related modalities. Emphasis is on early and timely publication. Primarily research-oriented, the journal also includes a wide variety of features of interest to clinical radiologists.