Mohanty Kartik, Saha Asim, Pal Smarajit, Mallick Palash, Chatterjee Sunil K, Foon Kenneth A, Bhattacharya-Chatterjee Malaya
Department of Internal Medicine, University of Cincinnati, The Vontz Center for Molecular Studies, 3125 Eden Avenue, Cincinnati, OH 45267, USA.
Breast Cancer Res Treat. 2007 Jul;104(1):1-11. doi: 10.1007/s10549-006-9391-9. Epub 2006 Sep 27.
Our goal is to apply an anti-idiotype (Id) antibody based vaccine approach for the treatment of Her-2/neu-positive human cancer. Amplification and/or over-expression of Her-2/neu occur in multiple human malignancies and are associated with poor prognosis. Her-2/neu proto-oncogene is a suitable target for cancer immunotherapy. We have developed and characterized a murine monoclonal anti-Id antibody, 6D12 that mimics a specific epitope of Her-2/neu and can be used as a surrogate antigen for Her-2/neu. In this study, the efficacy of 6D12 as a tumor vaccine was evaluated in a murine tumor model. Immunization of immunocompetent C57BL/6 mice with 6D12 conjugated to keyhole limpet hemocyanin and mixed with Freund's adjuvant or 6D12 combined with the adjuvant QS21 induced anti-6D12 as well as anti-Her-2/neu immunity. Her-2/neu-positive human breast carcinoma cells, SK-BR-3 reacted with immunized mice sera as determined by ELISA and flow cytometry. Flow cytometry analysis also demonstrated strong reactivity of immunized mice sera with human Her-2/neu transfected EL4 cells (EL4-Her-2), but no reactivity with nontransfected parental EL4 cells. Antibody dependent cellular cytotoxicity against EL4-Her-2 cells was also observed in presence of immune sera. Mice immunized with 6D12 were protected against a challenge with lethal doses of EL4-Her-2 cells, whereas no protection was observed against parental EL4 cells or when mice were immunized with an unrelated anti-Id antibody and challenged with EL4-Her-2 cells. These data suggest that anti-Id 6D12 vaccine can induce protective Her-2/neu specific antitumor immunity and may serve as a potential network antigen for the treatment of patients with Her-2/neu-positive tumors.
我们的目标是应用基于抗独特型(Id)抗体的疫苗方法来治疗Her-2/neu阳性的人类癌症。Her-2/neu的扩增和/或过表达发生在多种人类恶性肿瘤中,并与预后不良相关。Her-2/neu原癌基因是癌症免疫治疗的合适靶点。我们已经开发并鉴定了一种鼠单克隆抗Id抗体6D12,它模拟Her-2/neu的特定表位,可作为Her-2/neu的替代抗原。在本研究中,在鼠肿瘤模型中评估了6D12作为肿瘤疫苗的疗效。用与钥孔血蓝蛋白偶联并与弗氏佐剂混合的6D12或与佐剂QS21联合的6D12免疫有免疫活性的C57BL/6小鼠,可诱导产生抗6D12以及抗Her-2/neu免疫。通过ELISA和流式细胞术测定,Her-2/neu阳性的人乳腺癌细胞SK-BR-3与免疫小鼠血清发生反应。流式细胞术分析还表明,免疫小鼠血清与人Her-2/neu转染的EL4细胞(EL4-Her-2)有强烈反应,但与未转染的亲本EL4细胞无反应。在免疫血清存在的情况下,也观察到对EL4-Her-2细胞的抗体依赖性细胞毒性。用6D12免疫的小鼠对致死剂量的EL4-Her-2细胞攻击具有抵抗力,而对亲本EL4细胞攻击无抵抗力,在用无关抗Id抗体免疫并攻击EL4-Her-2细胞的小鼠中也未观察到保护作用。这些数据表明,抗Id 6D12疫苗可诱导保护性的Her-2/neu特异性抗肿瘤免疫,可能作为治疗Her-2/neu阳性肿瘤患者的潜在网络抗原。