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人前列腺干细胞抗原和 HSP70 融合蛋白疫苗抑制表达前列腺干细胞抗原的肿瘤在小鼠中的生长。

Human prostate stem cell antigen and HSP70 fusion protein vaccine inhibits prostate stem cell antigen-expressing tumor growth in mice.

机构信息

Clinical Laboratory Center, PLA Air Force General Hospital, Beijing, China.

出版信息

Cancer Biother Radiopharm. 2013 Jun;28(5):391-7. doi: 10.1089/cbr.2012.1357. Epub 2013 May 23.

DOI:10.1089/cbr.2012.1357
PMID:23701419
Abstract

Prostate stem cell antigen (PSCA) has been considered a potentially worthwhile target for prostate cancer therapy with its overexpression in both androgen-dependent and androgen-independent prostate cancers. However, PSCA is an autoantigen that can evoke immunological tolerance and hardly incite effective immunologic response. In this study, we sought to construct the fusion protein vaccines based on PSCA and heat shock protein 70 (HSP70) and to evaluate their immune responses and therapeutic efficacy. A series of recombinant proteins were prepared, and then, the male C57BL/6 mice were immunized subcutaneously by inoculation with RM-PSCA/Luc cells. The PSCA-specific cellular immune responses were monitored with ELISPOT and intracellular cytokines staining assay, and ELISA assay was used to detect humoral immune responses. The tumor growth was observed by in vivo bioluminescence imaging. The results showed that the mice vaccinated with PSCA-HSP could induce the PSCA-specific cellular and humoral immune responses. Tumor progression could be quantitatively monitored by in vivo bioluminescence imaging. Animal experiments showed that PSCA-HSP could inhibit the growth of PSCA-expressing tumors and prolong the survival time of vaccinated mice. This study supported and confirmed the potential of HSP70 as a chaperone for protein vaccines, and PSCA-HSP could be of potential value for prostate cancer treatment.

摘要

前列腺干细胞抗原 (PSCA) 在雄激素依赖性和雄激素非依赖性前列腺癌中均过度表达,因此被认为是前列腺癌治疗的一个有价值的潜在靶点。然而,PSCA 是一种自身抗原,可以引起免疫耐受,几乎不能引发有效的免疫反应。在这项研究中,我们试图构建基于 PSCA 和热休克蛋白 70 (HSP70) 的融合蛋白疫苗,并评估它们的免疫反应和治疗效果。制备了一系列重组蛋白,然后通过接种 RM-PSCA/Luc 细胞对雄性 C57BL/6 小鼠进行皮下免疫。通过 ELISPOT 和细胞内细胞因子染色分析监测 PSCA 特异性细胞免疫反应,通过 ELISA 分析检测体液免疫反应。通过体内生物发光成像观察肿瘤生长。结果表明,接种 PSCA-HSP 的小鼠可诱导 PSCA 特异性细胞和体液免疫反应。通过体内生物发光成像可以定量监测肿瘤进展。动物实验表明,PSCA-HSP 可以抑制表达 PSCA 的肿瘤的生长并延长接种小鼠的存活时间。这项研究支持并证实了 HSP70 作为蛋白疫苗伴侣的潜力,PSCA-HSP 可能对前列腺癌的治疗具有潜在价值。

相似文献

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Human prostate stem cell antigen and HSP70 fusion protein vaccine inhibits prostate stem cell antigen-expressing tumor growth in mice.人前列腺干细胞抗原和 HSP70 融合蛋白疫苗抑制表达前列腺干细胞抗原的肿瘤在小鼠中的生长。
Cancer Biother Radiopharm. 2013 Jun;28(5):391-7. doi: 10.1089/cbr.2012.1357. Epub 2013 May 23.
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Vaccination with recombinant adenoviruses and dendritic cells expressing prostate-specific antigens is effective in eliciting CTL and suppresses tumor growth in the experimental prostate cancer.用表达前列腺特异性抗原的重组腺病毒和树突状细胞进行疫苗接种,在实验性前列腺癌中可有效激发细胞毒性T淋巴细胞(CTL)并抑制肿瘤生长。
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A novel DNA/peptide combined vaccine induces PSCA-specific cytotoxic T-lymphocyte responses and suppresses tumor growth in experimental prostate cancer.一种新型的 DNA/肽联合疫苗可诱导 PSCA 特异性细胞毒性 T 淋巴细胞反应,并抑制实验性前列腺癌的肿瘤生长。
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Vaccination with a chaperone complex based on PSCA and GRP170 adjuvant enhances the CTL response and inhibits the tumor growth in mice.基于 PSCA 和 GRP170 佐剂的共伴侣复合物疫苗接种增强了 CTL 反应并抑制了小鼠肿瘤生长。
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Small interference RNA-mediated silencing of prostate stem cell antigen attenuates growth, reduces migration and invasion of human prostate cancer PC-3M cells.小干扰 RNA 介导的前列腺干细胞抗原沉默可减弱人前列腺癌 PC-3M 细胞的生长,减少迁移和侵袭。
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Prostate stem cell antigen vaccination induces a long-term protective immune response against prostate cancer in the absence of autoimmunity.前列腺干细胞抗原疫苗接种在无自身免疫的情况下可诱导针对前列腺癌的长期保护性免疫反应。
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