新型HPV16E7-HBcAg-Hsp65融合蛋白疫苗的有效治疗效果

Chao Zhang, Chenliang Zhou, Xiaoliang Wang, Xinxing Ma, Meijun Diao, Haitao Liu, Dan Xu, Jian Wei, Yuanxiang Jiang, Menghua Zhang, Lingyun Zhou, Jiang Fan, Ge Liu
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引用次数: 0

摘要

结果:TC-1在高剂量(30 μg)下均表现出较强的剂量依赖性治疗效果和提高率。vr111的三种融合成分都是诱导最佳抗肿瘤活性、CTL反应和T细胞增殖所必需的。肿瘤生长抑制和更高的小鼠存活率是以顺铂为基础的联合治疗的有益效果。此外,vr111疫苗的抗肿瘤效力与E7特异性CD8 + T细胞免疫应答显著相关,过继性淋巴细胞转移治疗也具有肿瘤生长抑制作用。结论:vr111是一种有效的HPV治疗性候选疫苗,在人乳头瘤病毒诱导的小鼠肿瘤模型中具有良好的抗肿瘤作用,可以考虑其用于宫颈癌的联合治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potent Therapeutic Efficacy of a Novel HPV16E7-HBcAg-Hsp65 Fusion Protein Vaccine
Results: In TC-1 showed potent dose dependent therapeutic efficacy against and improved rates in the and high doses (30 μg). The three fusion components of VR 111 were all necessary to induce the best anti-tumor activity, CTL response and T cell proliferation. The tumor growth inhibition and a higher mouse survival rate were among the beneficial effects of cisplatin-based combination treatment. Moreover, the anti-tumor potency of VR 111 vaccine was proved to be significantly associated with E7 specific CD8 + T cell immune response and the adoptive lymphocyte transfer therapy also showed tumor growth inhibition. Conclusion: The results confirmed VR 111 as a potent therapeutic HPV vaccine candidate with superior anti-tumor efficacy in a murine model of HPV-induced cancer which its potentials could be considered for combination therapies against cervical cancer.
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