HER2/neu的细胞外结构域是乳腺癌主动特异性免疫治疗的潜在免疫原。

B M Fendly, C Kotts, D Vetterlein, G D Lewis, M Winget, M E Carver, S R Watson, J Sarup, S Saks, A Ullrich
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引用次数: 0

摘要

原癌基因HER2/neu编码一种蛋白酪氨酸激酶(p185HER2),该蛋白与人类表皮生长因子受体同源。HER2/neu的扩增和/或过表达发生在多种人类恶性肿瘤中,似乎与一些乳腺癌和卵巢癌的进展有关。由于这一事实,HER2/neu是特定癌症治疗策略的一个有趣的靶点。一种这样的策略是主动特异性免疫治疗,其中免疫系统针对肿瘤细胞表达的特定抗原。我们在豚鼠模型中使用了一种分泌p185HER2细胞外结构域的转染细胞系作为her2衍生免疫原的来源。通过延迟型超敏反应监测,免疫动物产生了细胞免疫反应,免疫动物的抗血清特异性地抑制了过表达p185HER2的人乳腺肿瘤细胞的体外生长。这些数据为以HER2/neu原癌基因过表达为特征的癌症的免疫治疗方法提供了支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The extracellular domain of HER2/neu is a potential immunogen for active specific immunotherapy of breast cancer.

The proto-oncogene HER2/neu encodes a protein tyrosine kinase (p185HER2) that is homologous to the human epidermal growth factor receptor. Amplification and/or overexpression of HER2/neu occurs in multiple human malignancies and appears to be integrally involved in progression of some breast and ovarian cancers. Because of this fact, HER2/neu is an intriguing target for specific cancer therapeutic strategies. One such strategy is active specific immunotherapy, in which the immune system is targeted at specific antigens expressed by tumor cells. We have employed a transfected cell line that secretes the extracellular domain of p185HER2 as a source of HER2-derived immunogen in a guinea pig model. The immunized animals developed a cellular immune response, as monitored by delayed-type hypersensitivity, and antisera derived from immunized animals specifically inhibited the in vitro growth of human breast tumor cells overexpressing p185HER2. These data provide support for an immunotherapeutic approach to cancers characterized by overexpression of the HER2/neu proto-oncogene.

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