CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Expression of c-erb-B2 oncoprotein as a neoantigen strategy to repurpose anti-neu antibody therapy in a model of melanoma.
Expression of c-erb-B2 oncoprotein as a neoantigen strategy to repurpose anti-neu antibody therapy in a model of melanoma.
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本研究探索一种新策略:将通常与乳腺癌相关的生物标志物重新用于黑色素瘤。HER2/neu 是乳腺癌中研究充分的标志物,且已有有效的抗 HER2/neu 疗法。研究构建了编码 c-erb-B2(HER2/neu 的动物同源物)的慢病毒,并在体外转导 B16 黑色素瘤细胞,用于原位临床前小鼠模型,使 c-erb-B2 成为抗 c-erb-B2 单克隆抗体 7.16.4 的新抗原靶点。表达 c-erb-B2 的黑色素瘤被命名为 B16/neu。7.16.4 在体内对 B16/neu 产生具有统计学意义的抗肿瘤作用,该效应由 NK 细胞介导的抗体依赖性细胞介导的细胞毒作用实现。为进一步模拟表达 HER2/neu 不足 5% 的人类黑色素瘤,研究使用编码 c-erb-B2 的慢病毒在体内接种未处理的野生型 B16 肿瘤,并成功诱导 c-erb-B2 表达。联合 7.16.4 后再次观察到抗肿瘤作用;接受 c-erb-B2 慢病毒和 7.16.4 治疗的小鼠中,约 40% 达到完全临床缓解并长期存活。
本研究首次证明,可将 c-erb-B2 重新用作黑色素瘤的新抗原靶点。在新型抗 HER2/neu 抗体药物候选物疗效不断提高的当下,这些发现尤其具有意义。
In this study, we tested a novel approach of "repurposing" a biomarker typically associated with breast cancer for use in melanoma. HER2/neu is a well characterized biomarker in breast cancer for which effective anti-HER2/neu therapies are readily available.
We constructed a lentivirus encoding c-erb-B2 (the animal homolog to HER2/neu). This was used to transfect B16 melanoma in vitro for use in an orthotopic preclinical mouse model, which resulted in expression of c-erb-B2 as a neoantigen target for anti-c-erb-B2 monoclonal antibody (7. 16. 4). The c-erb-B2-expressing melanoma was designated B16/neu. 7. 16. 4 produced statistically significant in vivo anti-tumor responses against B16/neu. This effect was mediated by NK-cell antibody-dependent cell-mediated cytotoxicity.
To further model human melanoma (which expresses <5% HER2/neu), our c-erb-B2 encoding lentivirus was used to inoculate na ve (wild-type) B16 tumors in vivo , resulting in successful c-erb-B2 expression. When combined with 7. 16. 4, anti-tumor responses were again demonstrated where approximately 40% of mice treated with c-erb-B2 lentivirus and 7. 16. 4 achieved complete clinical response and long-term survival. For the first time, we demonstrated a novel strategy to repurpose c-erb-B2 as a neoantigen target for melanoma.
Our findings are particularly significant in the contemporary setting where newer anti-HER2/neu antibody-drug candidates have shown increased efficacy.
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