Augmentation of in vivo CMS5mHE tumor eradication by HER216-30, but not OVA323-339. Augmentation of in vivo CMS5mHE tumor eradication by HER216-30, but.

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Augmentation of in vivo CMS5mHE tumor eradication by HER216-30, but not OVA323-339. Augmentation of in vivo CMS5mHE tumor eradication by HER216-30, but not OVA323-339. (A) Pre-tumor cell injection. One week after the last peptide immunization described in Materials and Methods, mice were challenged i.v. with 1x106 CMS5mHE tumor cells. Twenty days after tumor inoculation, lung metastatic foci were counted under a dissecting microscope. The number of metastatic foci in mice immunized with OVA323-339 or HER216-30 in combination with HER263-71 was less than in mice immunized with HER263-71 alone or in untreated mice. In mice immunized with HER216-30 and HER263-71, markedly fewer metastatic foci were counted than in mice immunized with OVA323-339 and HER263-71. (B and C) Post-tumor cell injection. Four days after i.v. inoculation with 1x106 CMS5mHE tumor cells, mice were immunized with peptide on a weekly basis. Results similar to A were observed. Animal survival was also monitored up to 50 days following tumor inoculation. Only mice treated with HER216-30 and HER263-71 survived throughout the observation period. The number of foci represents the mean ± SD of five mice per group in A and B. Lijie Wang et al. Cancer Immun 2003;3:16 Copyright © 2003 by Hiroshi Shiku