Suppr超能文献

利用肿瘤靶向间充质干细胞和蛋白疫苗开发新型癌症免疫治疗平台。

The development of a novel cancer immunotherapeutic platform using tumor-targeting mesenchymal stem cells and a protein vaccine.

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.

出版信息

Mol Ther. 2011 Dec;19(12):2249-57. doi: 10.1038/mt.2011.152. Epub 2011 Jul 26.

Abstract

An ideal anticancer strategy should target only the malignant cells but spare the normal ones. In this regard, we established a platform, consisting of an antigen-delivering vehicle and a protein vaccine, for developing an immunotherapeutic approach with the potential for eliminating various cancer types. Mesenchymal stem cells (MSCs) have been demonstrated capable of targeting tumors and integrating into the stroma. Moreover, we have developed a protein vaccine PE(ΔIII)-E7-KDEL3 which specifically recognized E7 antigen and elicited immunity against cervical cancer. Taking advantage of tumor-homing property of MSCs and PE(ΔIII)-E7-KDEL3, we used E6/E7-immortalized human MSCs (KP-hMSCs) as an E7 antigen-delivering vehicle to test if this protein vaccine could effectively eliminate non-E7-expressing tumor cells. Animals which received combined treatment of KP-hMSCs and PE(ΔIII)-E7-KDEL3 demonstrated a significant inhibition of tumor growth and lung-metastasis when compared to PE(ΔIII)-E7-KDEL3 only and KP-hMSCs only groups. The efficiency of tumor suppression correlated positively to the specific immune response induced by PE(ΔIII)-E7-KDEL3. In addition, this combined treatment inhibited tumor growth via inducing apoptosis. Our findings indicated that KP-hMSCs could be used as a tumor-targeting device and mediate antitumor effect of PE(ΔIII)-E7-KDEL3. We believe this strategy could serve as a platform for developing a universal vaccine for different cancer types.

摘要

一种理想的抗癌策略应该只针对恶性细胞,而不影响正常细胞。在这方面,我们建立了一个平台,包括一个抗原递药载体和一个蛋白疫苗,用于开发一种具有消除各种癌症类型潜力的免疫治疗方法。间充质干细胞(MSCs)已被证明能够靶向肿瘤并整合到基质中。此外,我们已经开发了一种蛋白疫苗 PE(ΔIII)-E7-KDEL3,它能特异性识别 E7 抗原并引发针对宫颈癌的免疫反应。利用 MSCs 和 PE(ΔIII)-E7-KDEL3 的肿瘤归巢特性,我们使用 E6/E7-永生化人 MSCs(KP-hMSCs)作为 E7 抗原递药载体,来测试这种蛋白疫苗是否能有效消除非 E7 表达的肿瘤细胞。与单独使用 PE(ΔIII)-E7-KDEL3 和单独使用 KP-hMSCs 的动物相比,接受 KP-hMSCs 和 PE(ΔIII)-E7-KDEL3 联合治疗的动物的肿瘤生长和肺转移明显受到抑制。肿瘤抑制的效率与 PE(ΔIII)-E7-KDEL3 诱导的特异性免疫反应呈正相关。此外,这种联合治疗通过诱导细胞凋亡抑制肿瘤生长。我们的研究结果表明,KP-hMSCs 可用作肿瘤靶向装置,并介导 PE(ΔIII)-E7-KDEL3 的抗肿瘤作用。我们相信,这种策略可以作为开发针对不同癌症类型的通用疫苗的平台。

相似文献

引用本文的文献

8
Mesenchymal Stem Cells Beyond Regenerative Medicine.再生医学之外的间充质干细胞
Front Cell Dev Biol. 2020 Feb 18;8:72. doi: 10.3389/fcell.2020.00072. eCollection 2020.

本文引用的文献

2
Cancer statistics, 2009.2009年癌症统计数据。
CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49. doi: 10.3322/caac.20006. Epub 2009 May 27.
4
How tumours escape mass destruction.肿瘤如何逃避大规模破坏。
Oncogene. 2008 Oct 6;27(45):5894-903. doi: 10.1038/onc.2008.268.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验