文章摘要
Xia Chen,Xiaoming Zhang,Xiangji Lu,Meng Ren,Rina Su,Weishi Gao,Yanwei Gao. Enhancing the treatment effects of tumor cell purified autogenous heat shock protein 70-peptide complexes on HER-3-overexpressing breast cancer*. Oncol Transl Med, 2021, 7: 165-171.
增强自体热休克蛋白70-肿瘤肽复合物对HER-3阳性乳腺癌治疗效果的研究
Enhancing the treatment effects of tumor cell purified autogenous heat shock protein 70-peptide complexes on HER-3-overexpressing breast cancer*
Received:February 24, 2021  Revised:July 29, 2021
DOI:10.1007/s10330-021-0485-5
中文关键词: 热休克蛋白70-抗原肽复合物;Her-2蛋白;重组蛋白;树突状细胞;细胞免疫治疗
英文关键词: heat shock protein 70 peptide complexes (HSP70-PCs); HER-3 protein; recombinant protein; dendritic cells (DCs); cellular immunotherapy
基金项目:乳腺癌HSP70-HER谱对诱导自体特异性CD8+NKT细胞活性的影响
Author NameAffiliationPostcode
Xia Chen Inner Mongolia Red Cross Blood Center, Hohhot, Inner Mongolia 010010, China 010010
Xiaoming Zhang Inner Mongolia People’s Hospital, Hohhot, Inner Mongolia 010017, China 
Xiangji Lu Inner Mongolia Armed Police Hospital, Hohhot, Inner Mongolia 010010, China 
Meng Ren Inner Mongolia People’s Hospital, Hohhot, Inner Mongolia 010017, China 
Rina Su Inner Mongolia People’s Hospital, Hohhot, Inner Mongolia 010017, China 
Weishi Gao Inner Mongolia People’s Hospital, Hohhot, Inner Mongolia 010017, China * 
Yanwei Gao* Inner Mongolia People’s Hospital, Hohhot, Inner Mongolia 010017, China * 010017
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中文摘要:
  目的 探讨增强自体热休克蛋白70-肿瘤肽复合物对HER-3阳性乳腺癌患者治疗效果的方法。 方法 我们首先研究了HER-3在乳腺癌组织中的表达及其与患者肿瘤临床特征的关系。其次,我们从具有不同HER-2和HER-3表达的原发性乳腺癌细胞中纯化自体HSP70-PCs,并测定复合物诱导的自体树突状细胞和CD8+T细胞的抗肿瘤活性。再次,用重组人HSP70-HER-3蛋白复合物对从HER-3高表达乳腺癌细胞中纯化的自体HSP70-PCs进行干预,并检测其免疫活性。 结果 结果表明,HSP70-PCs与重组HSP70-HER-3蛋白复合物结合后,诱导自体CD8+T细胞杀伤HER-3阳性乳腺癌细胞的免疫活性明显强于自体HSP70-PCs。 结论 本研究为以HSP70-DC为基础的HER-3高表达乳腺癌患者的免疫治疗提供了新的方向。
英文摘要:
    Objective The aim of this study was to enhance the treatment effect of tumor purified autogenous heat shock protein 70-peptide complexes (HSP70-PCs) on HER-3-overexpressing breast cancer. Methods In this study, we first studied the expression of HER-3 in breast cancer tissues and its relationship with patient characteristics. We then purified HSP70-PCs from primary breast cancer cells with different HER-2 and HER-3 expression profiles and determined the cytotoxicity of autogenous dendritic cells (DCs) and CD8+ T cells induced by these complexes. Third, recombinant human HSP70-HER-3 protein complexes were used to inhibit the autogenous HSP70-PCs purified from HER-3–overexpressing breast cancer cells, and the resulting immunological response was examined. Results The results show that HSP70-PCs can be combined with recombinant HSP70-HER-3 protein complexes to induce stronger immunological responses than autogenous HSP70-PCs alone and that these treatments induce autogenous CD8+ T cell killing of HER-3-positive breast cancer cells. Conclusion These findings provide a new direction for HSP70-DC-based immunotherapy for patients with HER-3-overexpressing breast cancer.
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