Mach J P, Pèlegrin A, Folli S, Buchegger F
Institut de Biochimie, Université de Lausanne, Epalinges.
Bull Acad Natl Med. 1992 Jun;176(6):879-89.
While it is now well accepted that radiolabeled antibodies can be useful for tumour detection by immunoscintigraphy, the use of larger doses of more aggressive radioisotopes coupled to antibodies for radioimmunotherapy is still in its infancy. At the experimental level, our group has shown that the intravenous injection of large doses of 131I labeled F(ab')2 fragments from monoclonal anti-carcinoembryonic antigen (CEA) antibodies can eradicate well established human colon carcinoma xenografts in nude mice. At the clinical level, in a dosimetry study performed at the Institut Gustave Roussy, the same anti-CEA monoclonal antibodies and fragments, labeled with subtherapeutic doses of 131I, were injected in patients with liver metastases from colorectal carcinomas. Direct measurement of radioactivity in surgically resected liver metastases and normal liver confirmed the specificity of tumour localization of the antibodies, but also showed that the calculated radiation doses which could be delivered by injections of 200 to 300 mCi of 131I labeled antibodies or fragments, remained fairly low, in the range of 1,500 to 3,000 rads. This is obviously insufficient for a single modality treatment. An alternative approach is to inject radiolabeled antibodies intra peritoneally to treat peritoneal carcinomatosis. Several clinical studies using this strategy are presently under evaluation and suggest that positive results can be obtained when the tumour diameters are very small. In systemic radioimmunotherapy, positive results have been obtained in more radiosensitive types of malignancies such as B cell lymphomas by intravenous injection of antibodies directed against B cell differentiation markers or against idiotypic antigens from each lymphoma, and labeled with 131I or 90Y. The major directions of research for improvement of radioimmunotherapy include the design of genetically engineered new forms of humanized antibodies, the synthesis of original chelates for coupling new radioisotopes to antibodies and the development of two step strategies for immunolocalization of radioisotopes.
虽然放射性标记抗体可通过免疫闪烁显像用于肿瘤检测这一点现在已被广泛接受,但将更大剂量的更具攻击性的放射性同位素与抗体结合用于放射免疫治疗仍处于起步阶段。在实验层面,我们小组已表明,静脉注射大剂量的131I标记的抗癌胚抗原(CEA)单克隆抗体的F(ab')2片段能够根除裸鼠体内已形成的人结肠癌异种移植瘤。在临床层面,在古斯塔夫·鲁西研究所进行的一项剂量学研究中,将用亚治疗剂量的131I标记的相同抗CEA单克隆抗体和片段注射到患有结直肠癌肝转移的患者体内。对手术切除的肝转移灶和正常肝脏中的放射性进行直接测量,证实了抗体在肿瘤定位方面的特异性,但也表明,注射200至300 mCi的131I标记抗体或片段所计算出的辐射剂量仍然相当低,在1500至3000拉德范围内。这显然不足以进行单一方式的治疗。另一种方法是腹腔内注射放射性标记抗体来治疗腹膜癌病。目前有几项使用该策略的临床研究正在评估中,结果表明当肿瘤直径非常小时可获得阳性结果。在全身放射免疫治疗中,通过静脉注射针对B细胞分化标志物或针对每种淋巴瘤的独特型抗原且用131I或90Y标记的抗体,在B细胞淋巴瘤等对放射更敏感的恶性肿瘤类型中已取得阳性结果。放射免疫治疗改进的主要研究方向包括设计基因工程改造的新型人源化抗体、合成用于将新的放射性同位素与抗体偶联的新型螯合剂以及开发放射性同位素免疫定位的两步策略。