Lode H N, Reisfeld R A
Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Immunol Res. 2000;21(2-3):279-88. doi: 10.1385/IR:21:2-3:279.
Targeting of cytokines into the tumor microenvironment using antibody-cytokine fusion proteins, called immunocytokines, represents a novel approach in cancer immunotherapy. This article summarizes therapeutic efficacy and immune mechanisms involved in targeting interleukin-2 (IL-2) to neuroectodermal tumors using ganglioside GD2-specific antibody-IL-2 fusion protein (ch14.18-IL-2). Treatment of established melanoma metastases with ch14.18-IL-2 resulted in eradication of disease followed by a vaccination effect protecting mice from lethal challenges with wild-type tumor calls. In a syngeneic neuroblastoma model, targeted IL-2 was effective in the amplification of a weak memory immune response previously induced by IL-12 gene therapy using an engineered linear version of this heterodimeric cytokine. These findings show that targeted IL-2 may provide an effective tool in cancer immunotherapy and establish the missing link between T cell-mediated vaccination and objective clinical responses.
利用抗体 - 细胞因子融合蛋白(称为免疫细胞因子)将细胞因子靶向肿瘤微环境,是癌症免疫治疗中的一种新方法。本文总结了使用神经节苷脂GD2特异性抗体 - IL - 2融合蛋白(ch14.18 - IL - 2)将白细胞介素 - 2(IL - 2)靶向神经外胚层肿瘤所涉及的治疗效果和免疫机制。用ch14.18 - IL - 2治疗已建立的黑色素瘤转移灶可导致疾病根除,随后产生疫苗接种效应,保护小鼠免受野生型肿瘤细胞的致命攻击。在同基因神经母细胞瘤模型中,靶向IL - 2可有效增强先前使用工程化线性异二聚体细胞因子IL - 12基因疗法诱导的微弱记忆免疫反应。这些发现表明,靶向IL - 2可能为癌症免疫治疗提供一种有效工具,并建立T细胞介导的疫苗接种与客观临床反应之间缺失的联系。