The Development of a Novel Cancer Immunotherapeutic Platform Using Tumor-targeting Mesenchymal Stem Cells and a Protein Vaccine

被引:24
|
作者
Wei, Hon-Jian [2 ]
Wu, Alexander T. H. [3 ,4 ,5 ]
Hsu, Chung-Huei [6 ]
Lin, Yi-Ping [1 ]
Cheng, Wen-Fang [7 ]
Su, Ching-Hua [2 ]
Chiu, Wen-Ta [5 ]
Whang-Peng, Jacqueline [5 ,8 ]
Douglas, Frank L. [9 ]
Deng, Win-Ping [1 ,5 ]
机构
[1] Taipei Med Univ, Coll Oral Med, Grad Inst Biomed Mat & Engn, Taipei 110, Taiwan
[2] Taipei Med Univ, Coll Med, Grad Inst Med Sci, Taipei 110, Taiwan
[3] Taipei Med Univ, Coll Med, Sch Med, Radiat Dept, Taipei 110, Taiwan
[4] Taipei Med Univ Hosp, Ctr Canc, Translat Res Lab, Taipei, Taiwan
[5] Taipei Med Univ, Ctr Excellence Canc Res, Taipei 110, Taiwan
[6] Taipei Med Univ Hosp, Dept Nucl Med, Taipei, Taiwan
[7] Natl Taiwan Univ, Coll Med, Grad Inst Oncol, Taipei 10764, Taiwan
[8] Wan Fang Hosp, Div Canc Ctr, Taipei, Taiwan
[9] Austen BioInnovat Inst Akron, Akron, OH USA
关键词
CD4(+) T-CELLS; GENE-THERAPY; THYMIDINE KINASE; PURKINJE NEURONS; RAT MYOCARDIUM; HUMAN-MELANOMA; ANTIGEN; FUSION; STROMA; GANCICLOVIR;
D O I
10.1038/mt.2011.152
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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(Delta III)-E7-KDEL3 which specifically recognized E7 antigen and elicited immunity against cervical cancer. Taking advantage of tumor-homing property of MSCs and PE(Delta III)-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(Delta III)-E7-KDEL3 demonstrated a significant inhibition of tumor growth and lung-metastasis when compared to PE(Delta III)-E7-KDEL3 only and KP-hMSCs only groups. The efficiency of tumor suppression correlated positively to the specific immune response induced by PE(Delta III)-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(Delta III)-E7-KDEL3. We believe this strategy could serve as a platform for developing a universal vaccine for different cancer types. Received 12 November 2010; accepted 24 June 2011; published online 26 July 2011. doi:10.1038/mt.2011.152
引用
收藏
页码:2249 / 2257
页数:9
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