巯基还原介导的99mTc-IgG用于狒狒模型炎症病变的显像。

I C Dormehl, W K Louw, N Hugo, I F Redelinghuys, P J Fourie
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引用次数: 0

摘要

放射性标记程序可以改变免疫球蛋白分子Fc部分的结构,从而改变其体内免疫行为,损害其作为放射性药物治疗炎症病变的功效。本研究测试了巯基还原介导的99mTc人IgG对狒狒腹部/胸部或大腿的局灶性炎症病变的显像效果,无论是细菌还是化学诱导的。在静脉注射标记IgG后4 - 7小时,大腿病变处出现阳性图像。腹部/胸部病变从来都不是很清楚,主要是因为肾脏非常热。所有病变晚期(20小时)的显像较差,背景较高。虽然在IgG定位的机制中没有中性粒细胞和单核细胞的活性,但细菌诱导的病变更明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiol reduction-mediated 99mTc-IgG for scintigraphy of inflammatory lesions in the baboon model.

Radiolabeling procedures may modify the structure of the Fc portion of the immunoglobulin molecule in such a way that its in vivo immunological behavior may be altered and its efficacy as radiopharmaceutical for inflammatory lesions impaired. This study tested the efficacy of thiol reduction-mediated 99mTc human IgG for scintigraphy of focal inflammatory lesions, either bacterially or chemically induced and located either in the abdominal/thoracical region or in the thigh of baboons. Positive images were obtained in the thigh lesions between 4 and 7 hr after i.v. administration of the labeled IgG. The abdominal/thoracic lesions were never very clear, mostly because of very hot kidneys. Late visualization (20 hr) of all lesions was poor and a high background was present. Bacterially induced lesions were better visible, although no neutrophil nor monocyte activity could be established in the mechanism of the IgG localization.

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