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用于放射免疫检测的抗纤维蛋白单克隆抗体:在大鼠模型系统中的初步评估

Anti-fibrin monoclonal antibodies for radioimmunodetection: preliminary assessment in a rat model system.

作者信息

Walker K Z, Khafagi F, Bautovich G J, Boniface G R, Bundesen P G, Rylatt D B

机构信息

Clinical Immunology Research Centre, Sydney University, N.S.W., Australia.

出版信息

Thromb Res. 1988 Nov 15;52(4):269-78. doi: 10.1016/0049-3848(88)90068-0.

DOI:10.1016/0049-3848(88)90068-0
PMID:3201401
Abstract

The D Dimer (DD) site formed by linkage of D domains from adjacent fibrin (FN) molecules is unique to cross-linked FN and its degradation products and is not found in FN monomer or fibrinogen (FB). Thus monoclonal antibodies (MAb) reactive to DD should have a very suitable specificity for in vivo thrombus detection. Two anti-DD MAbs have been labelled with 131-I and assessed as scintigraphic agents in a normal rat model system. Each rat received 3 sc implants of antigen covalently coupled to Sepharose beads: 1) Human DD 2) Human FB 3) Glycine (GL) (control). Scintigraphic images taken 7 days after injection of 131-I anti DD MAb showed clear localisation of both anti-DD MAbs to the DD implant rather than to the FB or GL implants with no localisation in normal tissues. This was confirmed in biodistribution studies. Injection of anti-DD MAbs DD-3B6/22 and DD-IC3/108 resulted in DD: blood ratios of 10.4 +/- 0.6 and 4.9 +/- 0.3 respectively. These results suggest that anti-DD MAbs will have potential for thrombus radioimmunodetection.

摘要

由相邻纤维蛋白(FN)分子的D结构域连接形成的D-二聚体(DD)位点是交联FN及其降解产物所特有的,在FN单体或纤维蛋白原(FB)中不存在。因此,对DD有反应性的单克隆抗体(MAb)对体内血栓检测应具有非常合适的特异性。两种抗DD MAb已用131-I标记,并在正常大鼠模型系统中作为闪烁显像剂进行评估。每只大鼠接受3次皮下植入与琼脂糖珠共价偶联的抗原:1)人DD 2)人FB 3)甘氨酸(GL)(对照)。注射131-I抗DD MAb 7天后拍摄的闪烁显像图像显示,两种抗DD MAb均清晰定位于DD植入物,而非FB或GL植入物,且在正常组织中无定位。这在生物分布研究中得到了证实。注射抗DD MAb DD-3B6/22和DD-IC3/108后,DD与血液的比率分别为10.4±0.6和4.9±0.3。这些结果表明,抗DD MAb在血栓放射免疫检测方面具有潜力。

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引用本文的文献

1
Detection of experimental thrombi in rabbits with an 131I-labelled fibrin-specific monoclonal antibody.
Eur J Nucl Med. 1990;16(11):787-94. doi: 10.1007/BF00833012.