首页> 外文期刊>Journal of drug targeting >Single chain antibody vaccination in mice against human ovarian cancer enhanced by microspheres and cytokines.
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Single chain antibody vaccination in mice against human ovarian cancer enhanced by microspheres and cytokines.

机译:微球和细胞因子增强了小鼠抗人卵巢癌的单链抗体接种。

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摘要

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.
机译:使用单克隆抗体的实验研究表明,微球或细胞因子可以增强抗独特型免疫。这些策略背后的基本生理原理涉及抗原的持续释放和免疫系统的唤醒。在这项研究中,使用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。将识别人卵巢癌抗原CA125的单链抗体scFv-pDL1.0配制在微球中,单独注射或在存在集落刺激因子(GM-CSF)或肿瘤坏死因子(TNF-alpha)的情况下注射给小鼠。用配制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的产生增强,并且随后诱导抗抗独特型抗体的产生。这些结果通过给予包裹在微球中的GM-CSF或TNF-α的单链抗体,提高了癌症免疫疗法的可能性。

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