Signore A, Chianelli M, Toscano A, Monetini L, Ronga G, Nimmon C C, Britton K E, Pozzilli P, Negri M
Servizio di Medicina Nucleare, Policlinico Umberto I, Roma, Italy.
Nucl Med Commun. 1992 Oct;13(10):713-22.
The labelling of interleukin-2 (IL-2) with 123I and its in vivo application for imaging chronic pathological lymphocytic infiltrations are described. The lactoperoxidase/glucoseoxidase technique was the labelling method of choice leading to immunoreactive IL-2 with high specific activity. Labelled IL-2 was injected in diabetes-prone non-obese diabetic (NOD) mice with pancreatic lymphocytic infiltration. As control animals, Balb/c mice were used. As specificity control, monoclonal antibodies AMT13 and UCHT1, bovine serum albumin and alpha-lactalbumin were radioiodinated and injected in mice. Eighteen NOD mice and four control Balb/c mice were used for gamma camera imaging experiments. Fifty-four NOD and 20 Balb/c mice were used for time course single organ counting and autoradiography. Gamma camera images showed that radioactivity accumulated in the pancreatic region from the 10th minute onwards in NOD mice injected with 123I-IL-2 but not in Balb/c mice, or in NOD mice injected with control radiopharmaceuticals. These findings were confirmed by counting the radioactivity present in single organs. Autoradiography of NOD pancreas, after injection of labelled IL-2, showed that radioactivity was specifically associated with infiltrating lymphocytes. In conclusion, this technique is highly specific and easy to perform and we suggest its application in humans for in vivo detection of areas of lymphocytic infiltration.
描述了用¹²³I标记白细胞介素-2(IL-2)及其在体内用于慢性病理性淋巴细胞浸润成像的应用。乳过氧化物酶/葡萄糖氧化酶技术是首选的标记方法,可产生具有高比活性的免疫反应性IL-2。将标记的IL-2注射到患有胰腺淋巴细胞浸润的糖尿病易感性非肥胖糖尿病(NOD)小鼠体内。以Balb/c小鼠作为对照动物。作为特异性对照,将单克隆抗体AMT13和UCHT1、牛血清白蛋白和α-乳白蛋白进行放射性碘化并注射到小鼠体内。18只NOD小鼠和4只对照Balb/c小鼠用于γ相机成像实验。54只NOD小鼠和20只Balb/c小鼠用于时间进程单器官计数和放射自显影。γ相机图像显示,在注射¹²³I-IL-2的NOD小鼠中,从第10分钟起放射性在胰腺区域积聚,而在Balb/c小鼠或注射对照放射性药物的NOD小鼠中则没有。通过对单个器官中存在的放射性进行计数证实了这些发现。注射标记的IL-2后,NOD胰腺的放射自显影显示放射性与浸润淋巴细胞特异性相关。总之,该技术具有高度特异性且易于操作,我们建议将其应用于人体以体内检测淋巴细胞浸润区域。