Nakamura K
Department of Radiology, School of Medicine, Keio University.
Kaku Igaku. 1994 Sep;31(9):1133-40.
Radioimmunoscintigraphy (RIS) and radioimmunotherapy (RIT) have been exclusively studied for a dozen or so years, but few clinical RIS and RIT have been successful due to some limitations. In this review, two approaches are introduced to exceed the limitations; One is the modification of physiological and biochemical properties of tumors and the other is the modification of radiolabeled antibodies such as the development of labeling procedures and the production of new antibodies and fragments. The effect of interferon and vasoactive agents on the uptake of antibodies in tumors, and comparative biodistribution and pharmacokinetics of different radiolabeled antibodies and fragments which are produced in the new generation are reviewed. We believe that RIS and RIT could be evaluated precisely when these approaches are well applied to clinical patients.
放射免疫闪烁显像(RIS)和放射免疫治疗(RIT)已经被专门研究了十几年,但由于一些局限性,很少有临床RIS和RIT取得成功。在这篇综述中,介绍了两种克服这些局限性的方法;一种是改变肿瘤的生理和生化特性,另一种是改变放射性标记抗体,如标记程序的改进、新抗体和片段的生产。综述了干扰素和血管活性药物对肿瘤中抗体摄取的影响,以及新一代生产的不同放射性标记抗体和片段的比较生物分布和药代动力学。我们相信,当这些方法很好地应用于临床患者时,RIS和RIT可以得到精确评估。