Ram B P, Tyle P
American Cyanamid, Princeton, New Jersey 08540.
Pharm Res. 1987 Jun;4(3):181-8. doi: 10.1023/a:1016443725167.
Monoclonal antibodies can be produced against virtually any molecule, and unlike polyclonal antisera, they are highly specific. There has been great improvement in the monoclonal antibody production technique since its inception in 1975. The idea behind using monoclonals to direct cancer treatments is based on the fact that surfaces of tumor contain a wide variety of proteins, some of which are specific to the tumor type. Monoclonal antibodies that bind to such tumor-specific antigens could be used, either alone or as conjugates of drugs and toxins (immunoconjugates), to selectively seek out and destroy these tumor cells. Targeted drug delivery therapy of tumor using monoclonals or their conjugates has been reported by many investigators, and the early results are quite promising. However, many obstacles still have to be overcome before immunoconjugates become a valuable agent in the treatment of human diseases including cancer.
几乎可以针对任何分子生产单克隆抗体,并且与多克隆抗血清不同,它们具有高度特异性。自1975年单克隆抗体生产技术问世以来,该技术已有了很大改进。使用单克隆抗体指导癌症治疗背后的理念基于这样一个事实,即肿瘤表面含有多种蛋白质,其中一些是肿瘤类型所特有的。与这类肿瘤特异性抗原结合的单克隆抗体可以单独使用,也可以作为药物和毒素的缀合物(免疫缀合物)使用,以选择性地寻找并摧毁这些肿瘤细胞。许多研究人员报道了使用单克隆抗体或其缀合物进行肿瘤的靶向药物递送治疗,早期结果很有前景。然而,在免疫缀合物成为包括癌症在内的人类疾病治疗中有价值的药物之前,仍有许多障碍需要克服。