Ma Jie, Li Zheng, Luo Dong
State Key Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, PUMC, Panjiayuan, Beijing, People's Republic of China.
J Drug Target. 2003 Apr;11(3):169-76. doi: 10.1080/1061-1860310001598217.
Experimental studies using monoclonal antibody have demonstrated that anti-idiotypic immunity can be enhanced by microspheres or cytokines. The underlying physiological principles behind these strategies involve sustained release of antigen and arousal of the immune system. In this study, a murine model was used to investigate the combination effect of microspheres and cytokines on anti-idiotypic response. A single chain antibody scFv-pDL1.0, which recognizes the human ovarian cancer antigen CA125 was formulated in microspheres and injected to mice alone or in the presence of colony stimulating factor (GM-CSF) or tumor necrosis factor (TNF-alpha). The immunization of mice with formulated single chain antibody and cytokines resulted in enhanced production of anti-idiotypic antibody, and which subsequently induced the production of anti-anti-idiotypic antibody. These results raise the possibility of cancer immunotherapy by administration of single chain antibody encapsulated in microspheres with GM-CSF or TNF-alpha.
使用单克隆抗体的实验研究表明,抗独特型免疫可通过微球或细胞因子得到增强。这些策略背后的潜在生理原理涉及抗原的持续释放和免疫系统的激活。在本研究中,使用小鼠模型来研究微球和细胞因子对抗独特型反应的联合作用。一种识别人类卵巢癌抗原CA125的单链抗体scFv-pDL1.0被制备于微球中,并单独或在存在集落刺激因子(GM-CSF)或肿瘤坏死因子(TNF-α)的情况下注射到小鼠体内。用制备好的单链抗体和细胞因子对小鼠进行免疫导致抗独特型抗体产生增加,随后诱导了抗抗独特型抗体的产生。这些结果增加了通过给予包裹在微球中的单链抗体与GM-CSF或TNF-α进行癌症免疫治疗的可能性。