Goldenberg D M
Center for Molecular Medicine and Immunology, University of Medicine and Dentistry of New Jersey, Newark 07103.
Semin Nucl Med. 1989 Oct;19(4):332-9. doi: 10.1016/s0001-2998(89)80025-x.
This review discusses the current limitations and future prospects of radiolabeled antibodies in cancer imaging (radioimmunodetection, or RAID) and therapy (radioimmunotherapy, or RAIT). Aspects such as the antibody vehicle, antigen target, radiolabel, tumor, host, and RAID and RAIT procedures are considered. In the short timespan for the development of RAID, tumors as small as 0.5 cm, which are sometimes missed by other radiological methods, can now be imaged with antibody fragments labeled with suitable radionuclides (eg, 111In, 123I, and 99mTc), particularly when single photon emmission computed tomography (SPECT) scanning methods are employed. 99mTc is clearly the preferred label, and the recent development of simple and rapid methods to attach this isotope to antibodies should be a welcome advance for the more widespread use of RAID. In RAIT, radiosensitive neoplasms, such as lymphomas, are already showing impressive responses to 131I-labeled antilymphoma murine monoclonal antibodies. Therefore, the successful conjugation of beta- and alpha-emitters to "humanized" monoclonal antibodies should provide a new generation of promising cancer therapeutics.
本综述讨论了放射性标记抗体在癌症成像(放射免疫检测,即RAID)和治疗(放射免疫治疗,即RAIT)方面的当前局限性及未来前景。文中考虑了诸如抗体载体、抗原靶点、放射性标记、肿瘤、宿主以及RAID和RAIT程序等方面。在RAID发展的短时间内,小至0.5厘米的肿瘤(有时会被其他放射学方法漏检)现在可用标记有合适放射性核素(如111铟、123碘和99m锝)的抗体片段成像,特别是采用单光子发射计算机断层扫描(SPECT)扫描方法时。99m锝显然是首选标记,且将这种同位素连接到抗体的简单快速方法的近期发展,对于RAID更广泛的应用来说应是一项令人欣喜的进展。在RAIT中,对放射性敏感的肿瘤,如淋巴瘤,已显示出对131碘标记的抗淋巴瘤鼠单克隆抗体有令人瞩目的反应。因此,将β和α发射体成功偶联到“人源化”单克隆抗体上,应能提供新一代有前景的癌症治疗药物。