Antitumor effect of adenoviral vector prime protein boost immunity targeting the MUC1 VNTRs

Wang,Yuqian; Liu,Chenlu; Xia,Qiu; Wang,Peng; Li,Bo; Lu,Zhenzhen; Sun,Jiaxi; Wu,Hui; Yu,Bin; Wu,Jiaxin; Yu,Xianghui; Kong,Wei; Zhang,Haihong; Cong,Xianling

doi:10.3892/or.2013.2950

2014-March Volume 31 Issue 3

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2014-March Volume 31 Issue 3

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Article

Antitumor effect of adenoviral vector prime protein boost immunity targeting the MUC1 VNTRs

Authors:
- Yuqian Wang
- Chenlu Liu
- Qiu Xia
- Peng Wang
- Bo Li
- Zhenzhen Lu
- Jiaxi Sun
- Hui Wu
- Bin Yu
- Jiaxin Wu
- Xianghui Yu
- Wei Kong
- Haihong Zhang
- Xianling Cong
View Affiliations / Copyright

Affiliations: Science Research Center, China-Japan Union Hospital, Jilin University, Changchun 130012, P.R. China, National Engineering Laboratory of AIDS Vaccine, College of Life Science, Jilin University, Changchun 130012, P.R. China, High School affiliated with Jilin University, Changchun 130012, P.R. China
Pages: 1437-1444
|
Published online on: December 30, 2013

https://doi.org/10.3892/or.2013.2950
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Abstract

Mucin 1 (MUC1) is a tumor-associated antigen that is overexpressed in several adenocarcinomas. However, clinical trials with MUC1 showed that MUC1 is a relatively poor immunogen in humans. In view of the low immunogenicity of this protein vaccine, we designed a method based on an immunoadjuvant and immunization strategy to enhance the cellular immune response to this protein vaccine. DDA/MPL has been evaluated as an adjuvant to induce strong immunity for the tuberculosis vaccine. However, its adjuvant role combined with the vaccine targeting MUC1 in malignant carcinomas has not previously been reported. Our previous study showed that adenovirus prime protein boost vaccination could significantly enhance the cellular immunity and antitumor efficacy. In our study, we used MUC1 VNTRs as the target of cancer vaccine and DDA/MPL as the adjuvant to enhancing the cellular immunity of recombinant MUC1 protein vaccine, and an AD-9M adenoviral vector prime-recombinant protein and DDA/MPL boost (designated MUC-1 VPP vaccine) strategy was studied to enhance the antitumor efficacy. The results demonstrated that antigen-specific IFN-γ-secreting T cells were increased by 2-fold, and cytotoxic T lymphocytes (CTLs) were induced effectively when the protein vaccine was combined with the DDA/MPL adjuvant. Moreover, the vaccination induced nearly 60% inhibition of the growth of B16 melanoma in mice and prolonged the survival of tumor-bearing mice. The inhibition was correlated with the specific immune responses induced by the MUC1 VPP vaccine. The data suggested that DDA/MPL-adjuvant MUC-1 VPP vaccine may be developed into effective tumor vaccines for melanomas and possibly for other tumors expressing MUC1 protein.

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Journals

International Journal of Molecular Medicine

International Journal of Oncology

Molecular Medicine Reports

Oncology Reports

Experimental and Therapeutic Medicine

Oncology Letters

Biomedical Reports

Molecular and Clinical Oncology

World Academy of Sciences Journal

International Journal of Functional Nutrition

International Journal of Epigenetics

Medicine International

Antitumor effect of adenoviral vector prime protein boost immunity targeting the MUC1 VNTRs

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Abstract

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