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使用123I标记的抗粒细胞抗体对粒细胞进行体内标记。

In vivo labelling of granulocytes using 123I-tagged anti-granulocyte antibodies.

作者信息

Seybold K

机构信息

Department of Nuclear Medicine, Kantonsspital, Aarau, Switzerland.

出版信息

Nucl Med Commun. 1988 Oct;9(10):745-52. doi: 10.1097/00006231-198810000-00011.

Abstract

On the basis of previous work with various monoclonal antibodies (Mab) raised against carcino-embryonic antigen (CEA), the anti-CEA Mab 47 was identified which selectively reacted with a surface glycoprotein (95 kDa; NCA 95) of normal human granulocytes. This new tracer was quality tested and radioiodinated with 123I (123I Mab 47) for clinical use according to established procedures. Extended in vitro studies revealed a high selectivity for granulocytes without inhibiting their vital functions. In vivo cell binding to the granulocyte pool was completed very rapidly and remained unchanged over 24 h. For clinical use one dose consisting of 120 mcg of Mab was labelled with 4-5 mCi of 123I. Clinical interest was mainly concentrated on cases of osteomyelitis, infected allografts and abdominal and brain abscesses. After injection of 123I Mab 47, infectious lesions were usually seen after 3-5 h or could be excluded after 24 h. Because of high counting rates the image quality was excellent and single photon emission computerized tomography (SPECT) could be performed for an exact topographical localization of the lesions. No adverse reactions have been seen. It is concluded that there are distinct advantages of the new method compared with scanning of 111In-labelled leucocytes. However, despite this and the low dose of antibodies administered, we recommend restriction of immunoscintigraphy of infectious lesions before a clinically relevant immunization can be excluded.

摘要

基于先前使用针对癌胚抗原(CEA)产生的各种单克隆抗体(Mab)所做的工作,鉴定出了抗CEA Mab 47,它能与正常人粒细胞的一种表面糖蛋白(95 kDa;NCA 95)发生选择性反应。这种新的示踪剂经过质量检测,并按照既定程序用123I进行放射性碘化(123I Mab 47)以供临床使用。广泛的体外研究表明,它对粒细胞具有高度选择性,且不抑制其重要功能。在体内,它与粒细胞池的细胞结合非常迅速,并且在24小时内保持不变。临床使用时,一剂由120 mcg Mab组成,用4 - 5 mCi的123I进行标记。临床兴趣主要集中在骨髓炎、感染的同种异体移植物以及腹部和脑脓肿病例。注射123I Mab 47后,感染性病变通常在3 - 5小时后可见,或者在24小时后可排除。由于计数率高,图像质量极佳,并且可以进行单光子发射计算机断层扫描(SPECT)以精确确定病变的地形定位。未观察到不良反应。得出的结论是,与111In标记白细胞扫描相比,新方法具有明显优势。然而,尽管如此且所给予的抗体剂量较低,但在排除临床相关免疫之前,我们建议限制对感染性病变的免疫闪烁成像。

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