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Updated: Aug 11, 2026

Preparation of Tumor Antigen-loaded Mature Dendritic Cells for Immunotherapy
Published on: August 1, 2013
[Immunological efficiency of DNA vaccine targeting dendritic cells against tumor]
Bo Zhu1, Xiao-ming Cheng, Yu-zhong Duan
1Cancer Center of Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China. oncology_bozhu@yahoo.com.cn
Aim:
To construct the DNA vaccine containing ovalbumin (OVA) and Fc fusion gene targeting dentritic cells (DCs) and evaluate its anti-tumor efficiency in an E.G7-OVA-bearing tumor model.
Methods:
Constructed OVA-Fc-pcDNA3.1 plasmids were transfected into CHO cells with lipofectamine and the in vitro expression of OVA-Fc was determined by flow cytometry and ELISA. (51)Cr-relaese assay was used to determine the anti-tumor activity of cytotoxic T lymphocytes (CTLs) from splenocytes of immunized mice. According to tumor volume and survival time of the mice, the therapeutic effect of this vaccine was evaluated in E.G7-OVA-bearing tumor model.
Results:
DNA sequencing and restriction endonuclease digestion analysis indicated that the recombinant expression vector OVA-Fc-pcDNA3.1 had been constructed successfully. OVA-Fc expression could be detected in CHO cells transfected with OVA-Fc-pcDNA3.1 by ELISA and flow cytometry. The DNA vaccine containing OVA-Fc fusion gene inhibited tumor's growth and prolonged the time of tumor-bearing mice due to elicit the CTL-mediated anti-tumor immunity.
Conclusion:
OVA-Fc-pcDNA3.1 DNA vaccine targeting dendritic cells can elicit the CTL-mediated anti-tumor immunity, which lays the foundation for further clinical experiments.
Insights
This study developed a novel DNA vaccine, OVA-Fc-pcDNA3.1, targeting dendritic cells. The vaccine demonstrated significant anti-tumor efficiency by eliciting cytotoxic T lymphocyte-mediated immunity in a mouse model.
Area of Science:
- Immunology
- Molecular Biology
- Biotechnology
Context:
- Cancer immunotherapy research focuses on developing effective strategies against tumors.
- DNA vaccines offer a promising platform for inducing targeted immune responses.
- Ovalbumin (OVA) and Fc fusion proteins are utilized for enhanced antigen presentation and immune stimulation.
Purpose:
- To construct a DNA vaccine encoding an ovalbumin (OVA) and Fc fusion gene designed to target dendritic cells (DCs).
- To evaluate the anti-tumor efficacy of this novel DNA vaccine in a murine E.G7-OVA tumor model.
Summary:
- The recombinant expression vector OVA-Fc-pcDNA3.1 was successfully constructed and confirmed through DNA sequencing and restriction digestion.
- In vitro expression of the OVA-Fc fusion protein was validated in transfected cells using ELISA and flow cytometry.
- The DNA vaccine demonstrated significant anti-tumor activity by inhibiting tumor growth and prolonging survival in tumor-bearing mice, attributed to the induction of cytotoxic T lymphocyte (CTL)-mediated immunity.
Impact:
- The developed OVA-Fc-pcDNA3.1 DNA vaccine successfully elicits CTL-mediated anti-tumor immunity.
- This research provides a strong foundation for future clinical investigations into DNA vaccine-based cancer therapies.
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