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使用99锝标记单克隆抗体对肿瘤进行免疫闪烁显像:综述

Immunoscintigraphy of tumours using 99Tcm-labelled monoclonal antibodies: a review.

作者信息

Reilly R M

机构信息

Division of Nuclear Medicine, Toronto Hospital, Ontario, Canada.

出版信息

Nucl Med Commun. 1993 May;14(5):347-59. doi: 10.1097/00006231-199305000-00002.

Abstract

99Tcm is the optimum radionuclide for imaging in nuclear medicine due to its superior physical properties (E gamma of 140 keV and t1/2 of 6 h). Several techniques have recently been developed for labelling monoclonal antibodies with 99Tcm for immunoscintigraphy of human malignancies. These techniques primarily consist of either direct labelling of endogenous sulphydryl groups on the immunoglobulin with 99Tcm or indirect labelling through conjugation of a preformed 99Tcm-chelate. Direct methods offer the best promise for a one-step labelling kit but the 99Tcm-antibody may be unstable in vivo. This instability has been advantageous, however, in reducing blood background radioactivity and achieving sufficiently high tumour/blood ratios for clinical imaging. Over 1200 patients have been studied with 99Tcm-labelled monoclonal antibodies in the past decade. The majority of studies have been carried out in melanoma or colon cancer but other malignancies have also been investigated. The sensitivity has been variable and depended both on the size of the lesion and its location. Single photon emission computed tomographic imaging was helpful in some instances. Further study of labelling techniques and their effect on the pharmacokinetics of 99Tcm-labelled monoclonal antibodies as well as additional clinical evaluation of these agents is indicated.

摘要

由于锝-99m(99Tcm)具有优越的物理性质(γ射线能量为140keV,半衰期为6小时),它是核医学成像的最佳放射性核素。最近已开发出几种用99Tcm标记单克隆抗体以用于人类恶性肿瘤免疫闪烁成像的技术。这些技术主要包括用99Tcm直接标记免疫球蛋白上的内源性巯基或通过预先形成的99Tcm螯合物的共轭进行间接标记。直接方法为一步标记试剂盒提供了最好的前景,但99Tcm标记的抗体在体内可能不稳定。然而,这种不稳定性在降低血液本底放射性和实现足够高的肿瘤/血液比值以进行临床成像方面具有优势。在过去十年中,已有超过1200名患者接受了99Tcm标记的单克隆抗体研究。大多数研究是在黑色素瘤或结肠癌中进行的,但也对其他恶性肿瘤进行了研究。敏感性各不相同,取决于病变的大小及其位置。单光子发射计算机断层成像在某些情况下是有帮助的。需要进一步研究标记技术及其对99Tcm标记的单克隆抗体药代动力学的影响,以及对这些药物进行更多的临床评估。

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