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使用特异性抗体快速清除放射性标记肿瘤成像蛋白的循环血液背景。

Use of specific antibody for rapid clearance of circulating blood background from radiolabeled tumor imaging proteins.

作者信息

Goodwin D, Meares C, Diamanti C, McCall M, Lai C, Torti F, McTigue M, Martin B

出版信息

Eur J Nucl Med. 1984;9(5):209-15. doi: 10.1007/BF00448541.

Abstract

A major problem that arises when radiolabeled serum proteins are used for tumor imaging is the presence of a large amount of circulating background activity that persists for several days. This delays imaging for at least 2 days following injection and necessitates computer subtraction of simulated background (second radiopharmaceutical injection) which introduces artifacts that are difficult to control. We propose here the injection of specific antibody immediately before imaging as an alternate way of reducing blood background through clearance of the immune complex by the liver. 111In-alkyl human transferrin and IgG were injected IV in BALB/c tumor mice, and followed in 18 h by anti-human transferrin and anti-human IgG antibody IV. Two hours later, the tumor and organ distribution of activity was compared with control mice not receiving antibody. 111In-transferrin blood activity was reduced to 1/48 of control with no decrease in tumor concentration: as a result, the tumor to blood ratio increased from 1.4:1 to 78:1. 111In-IgG blood activity was reduced to 1/17 of control, again with no decrease in tumor. The tumor to blood ratios increased from 0.7:1 to 17:1. The liver picked up most of the blood activity with none of the complex going to spleen, bone marrow, or kidney. Dog experiments showed clearance of blood was 90% complete in less than 15 min following antibody injection. Simultaneous scintillation images showed complete clearance of activity from the heart and great vessels in the chest and neck, and over the abdomen, with a concomitant increase in liver activity but no increase in spleen, kidney, or bone marrow activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当使用放射性标记的血清蛋白进行肿瘤成像时,会出现一个主要问题,即存在大量持续数天的循环背景活性。这会在注射后至少延迟2天进行成像,并且需要对模拟背景(第二次放射性药物注射)进行计算机减法处理,这会引入难以控制的伪影。我们在此提出在成像前立即注射特异性抗体,作为通过肝脏清除免疫复合物来降低血液背景的另一种方法。将111In-烷基人转铁蛋白和IgG静脉注射到BALB/c肿瘤小鼠体内,并在18小时后静脉注射抗人转铁蛋白和抗人IgG抗体。两小时后,将活性的肿瘤和器官分布与未接受抗体的对照小鼠进行比较。111In-转铁蛋白的血液活性降至对照的1/48,而肿瘤浓度没有降低:结果,肿瘤与血液的比率从1.4:1增加到78:1。111In-IgG的血液活性降至对照的1/17,肿瘤同样没有减少。肿瘤与血液的比率从0.7:1增加到17:1。肝脏摄取了大部分血液活性,没有复合物进入脾脏、骨髓或肾脏。犬实验表明,抗体注射后不到15分钟,血液清除率达到90%。同时闪烁图像显示,胸部和颈部的心脏和大血管以及腹部的活性完全清除,同时肝脏活性增加,但脾脏、肾脏或骨髓活性没有增加。(摘要截断于250字)

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