Therapeutic MUC1-Based Cancer Vaccine Expressed in Flagella-Efficacy in an Aggressive Model of Breast Cancer

Nathalie Machluf, R. Arnon
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引用次数: 8

Abstract

MUC1, a tumor-associated antigen overexpressed in many carcinomas, represents a candidate of choice for cancer immunotherapy. Flagella-based MUC1 vaccines were tested in therapeutic setting in two aggressive breast cancer models, comprising the implantation of the 4T1-MUC1 cell line in either Balb/c, or Human MUC1 transgenic mice in which spontaneous metastases occurs. Recombinant flagella carrying only 7 amino acid of MUC1 elicited therapeutic activity, affecting both the growth of established growing tumors and the number of metastases. Higher therapeutic activity was achieved with an additional recombinant flagella designed with the SYFPEITHI algorithm. The vaccines triggered a Th1 response against MUC1 with no evident autoimmune response towards healthy MUC1-expressing tissues. Recombinant flagella carrying a 25-residue fragment of MUC1, induced the most effective response, as evidenced by a significant reduction of both the size and growth rate of the tumor as well as by the lower number of metastases, and expanding life span of vaccinated mice.
基于鞭毛表达muc1的治疗性肿瘤疫苗在侵袭性乳腺癌模型中的疗效
MUC1是一种在许多肿瘤中过表达的肿瘤相关抗原,代表了癌症免疫治疗的候选选择。在两种侵袭性乳腺癌模型中,基于鞭毛的MUC1疫苗在治疗环境中进行了测试,包括将4T1-MUC1细胞系植入Balb/c或人类MUC1转基因小鼠中,这些小鼠会发生自发转移。仅携带MUC1 7个氨基酸的重组鞭毛可激发治疗活性,既影响已建立的生长肿瘤的生长,也影响转移瘤的数量。用SYFPEITHI算法设计的另一个重组鞭毛获得了更高的治疗活性。这些疫苗触发了针对MUC1的Th1应答,而对表达MUC1的健康组织没有明显的自身免疫应答。携带MUC1 25残基片段的重组鞭毛诱导了最有效的反应,这证明了肿瘤的大小和生长速度显著降低,转移数量减少,并延长了接种小鼠的寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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