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

TitleThe development of a novel cancer immunotherapeutic platform using tumor-targeting mesenchymal stem cells and a protein vaccine.
Publication TypeJournal Article
Year of Publication2011
AuthorsWei H-J, Wu ATH, Hsu C-H, Lin Y-P, Cheng W-F, Su C-H, Chiu W-T, Whang-Peng J, Douglas FL, Deng W-P
JournalMol Ther
Volume19
Issue12
Pagination2249-57
Date Published2011 Dec
ISSN1525-0024
KeywordsADP Ribose Transferases, Animals, Apoptosis, Bacterial Toxins, Blotting, Western, CD8-Positive T-Lymphocytes, Enzyme-Linked Immunosorbent Assay, Exotoxins, Female, Fibrosarcoma, Genes, MHC Class I, Humans, Image Processing, Computer-Assisted, Lung Neoplasms, Mesenchymal Stromal Cells, Mice, Middle Aged, Oncogene Proteins, Viral, Papillomaviridae, Papillomavirus E7 Proteins, Papillomavirus Infections, Papillomavirus Vaccines, Peptide Fragments, Real-Time Polymerase Chain Reaction, RNA, Messenger, Sarcoma, Experimental, T-Lymphocytes, Cytotoxic, Virulence Factors
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.

DOI10.1038/mt.2011.152
Alternate JournalMol. Ther.
PubMed ID21792181
PubMed Central IDPMC3242654

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