Zhu Shiguo, Li Shulin
Department of Comparative Biomedical Sciences, Louisiana State University, Baton Rouge, LA, USA.
Methods Mol Biol. 2008;423:327-37. doi: 10.1007/978-1-59745-194-9_25.
Interleukin 12 (IL-12) is effective in treating systemic microscopic malignancies by inducing T helper 1 (T(H)1) response, inhibiting angiogenesis, and triggering secondary cytokine production. Unfortunately, daily systemic administration of an acute dose of IL-12 protein is very costly and severely toxic. Here, a simple, economic, and less toxic approach, intramuscular administration of IL-12 gene, is provided for treating tumors in three tumor models. The results indicate that intramuscular administration of IL-12 encoding plasmid DNA via electroporation is a promising technology for treating systemic residual malignancies (less than 3-5 mm in diameter), as illustrated by the inhibition of tumor growth and lung metastases as well as the extension of survival rate. This approach is not effective in treating tumors larger than 3-5 mm in diameter.
白细胞介素12(IL-12)通过诱导辅助性T细胞1(TH1)反应、抑制血管生成和触发次级细胞因子产生,在治疗全身性微小恶性肿瘤方面有效。不幸的是,每日全身性给予急性剂量的IL-12蛋白成本非常高且毒性严重。在此,提供了一种简单、经济且毒性较小的方法,即肌肉注射IL-12基因,用于在三种肿瘤模型中治疗肿瘤。结果表明,通过电穿孔肌肉注射编码IL-12的质粒DNA是一种治疗全身性残留恶性肿瘤(直径小于3 - 5毫米)的有前景的技术,这表现为肿瘤生长和肺转移受到抑制以及存活率提高。这种方法在治疗直径大于3 - 5毫米的肿瘤时无效。