Department of Gastroenterology and Hepatology, Brighton and Sussex University Hospitals NHS Trust, Brighton, U.K.
Department of Medicine, Brighton and Sussex Medical School, Brighton, U.K.
Biosci Rep. 2018 Jul 31;38(4). doi: 10.1042/BSR20180466. Print 2018 Aug 31.
The study's aim was to image severe alcoholic hepatitis (SAH) using In-labelled leucocytes with two objectives in mind: firstly for non-invasive diagnosis and secondly to provide a platform for experimental therapies aiming to inhibit intrahepatic neutrophil migration. In-leucocyte scintigraphy was performed 30 min and 24 h post-injection in 19 patients with SAH, 14 abstinent patients with alcohol-related cirrhosis and 11 normal controls. Eleven with SAH and seven with cirrhosis also had Tc-nanocolloid scintigraphy. Change in hepatic In radioactivity was expressed as decay-corrected 24 h:30 min count ratio and, in SAH, compared with histological grading of steatohepatitis and expression of granulocyte marker, CD15. Hepatic microautoradiography on biopsy specimens obtained 24 h post-injection of In-leucocytes was performed in one patient. Median 24 h:30 min hepatic In activity ratio was higher in SAH (2.5 (interquartile range (IQR): 1.7-4.0) compared with cirrhotics and normal controls (1.0 (0.8-1.1) and 0.8 (0.7-0.9) respectively, <0.0001). In SAH, it correlated with CD15 expression (r = 0.62, =0.023) and was higher in marked compared with mild/moderate steatohepatitis (4.0 (3.0-4.6) compared with 1.8 (1.5-2.6), =0.006). Hepatic-to-splenic Tc count rate ratio was reduced in SAH (0.5 (0.4-1.4)) compared with cirrhotics (2.3( 0.6-3.0)) and three historic normal controls (4.2 (3.8-5.0); =0.003), consistent with impaired hepatic reticuloendothelial function. Scintigraphic findings in SAH included prominent lung radioactivity at 30 min, likely the result of neutrophil primimg. Microautoradiography demonstrated cell-associated In in areas of parenchymal neutrophil infiltration. In conclusion, In-leucocyte scintigraphy can non-invasively diagnose SAH and could provide a platform for evaluation of novel treatments aiming to inhibit intrahepatic neutrophil migration.
该研究旨在使用放射性核素标记的白细胞对严重酒精性肝炎(SAH)进行成像,目的有二:一是进行非侵入性诊断,二是为旨在抑制肝内中性粒细胞迁移的实验性治疗提供平台。对 19 例 SAH 患者、14 例酒精性肝硬化戒断患者和 11 例正常对照者,在注射后 30 分钟和 24 小时进行放射性核素标记白细胞闪烁扫描。11 例 SAH 患者和 7 例肝硬化患者还进行了 Tc-胶体闪烁扫描。用放射性核素标记白细胞闪烁扫描术检测 SAH 患者的肝内放射性核素变化,以校正 24 小时与 30 分钟计数的比值表示,并与组织学脂肪性肝炎分级和粒细胞标记物 CD15 的表达进行比较。对 1 例患者注射放射性核素标记白细胞 24 小时后行肝活检标本微放射自显影。SAH 患者 24 小时与 30 分钟肝内放射性核素比值中位数(2.5(四分位数间距(IQR):1.7-4.0)高于肝硬化患者(1.0(0.8-1.1)和正常对照组(0.8(0.7-0.9),<0.0001)。在 SAH 患者中,它与 CD15 表达相关(r = 0.62,=0.023),在明显脂肪性肝炎中比轻度/中度脂肪性肝炎高(4.0(3.0-4.6)比 1.8(1.5-2.6),=0.006)。SAH 患者肝脾 Tc 计数比值(0.5(0.4-1.4))较肝硬化患者(2.3(0.6-3.0))和 3 例历史正常对照者(4.2(3.8-5.0);=0.003)低,提示肝网状内皮细胞功能受损。SAH 的闪烁扫描表现包括 30 分钟时肺放射性明显增加,可能是中性粒细胞启动的结果。微放射自显影显示细胞相关放射性核素在实质中性粒细胞浸润区域。总之,放射性核素标记白细胞闪烁扫描术可无创性诊断 SAH,并为评估旨在抑制肝内中性粒细胞迁移的新治疗方法提供平台。