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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Emerging cancer vaccines: the promise of genetic vectors
Luigi Aurisicchio1, Gennaro Ciliberto
1Takis, via di Castel Romano 100, 00128 Rome, Italy. aurisicchio@takis-it.it.
Abstract:
Therapeutic vaccination against cancer is an important approach which, when combined with other therapies, can improve long-term control of cancer. In fact, the induction of adaptive immune responses against Tumor Associated Antigens (TAAs) as well as innate immunity are important factors for tumor stabilization/eradication. A variety of immunization technologies have been explored in last decades and are currently under active evaluation, such as cell-based, protein, peptide and heat-shock protein-based cancer vaccines. Genetic vaccines are emerging as promising methodologies to elicit immune responses against a wide variety of antigens, including TAAs. Amongst these, Adenovirus (Ad)-based vectors show excellent immunogenicity profile and have achieved immunological proof of concept in humans. In vivo electroporation of plasmid DNA (DNA-EP) is also a desirable vaccine technology for cancer vaccines, as it is repeatable several times, a parameter required for the long-term maintenance of anti-tumor immunity. Recent findings show that combinations of different modalities of immunization (heterologous prime/boost) are able to induce superior immune reactions as compared to single-modality vaccines. In this review, we will discuss the challenges and requirements of emerging cancer vaccines, particularly focusing on the genetic cancer vaccines currently under active development and the promise shown by Ad and DNA-EP heterologous prime-boost.
Insights
Therapeutic cancer vaccines, especially genetic ones like Adenovirus (Ad) and DNA electroporation (DNA-EP), show promise. Combining these methods (heterologous prime-boost) can significantly enhance anti-tumor immune responses for better cancer control.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Therapeutic cancer vaccination is crucial for long-term cancer control, often in combination with other treatments.
- Induction of adaptive and innate immune responses against Tumor Associated Antigens (TAAs) is key for tumor stabilization and eradication.
- Various vaccine technologies, including cell-based, protein, peptide, and heat-shock protein vaccines, have been explored.
Purpose of the Study:
- To review emerging cancer vaccine technologies, focusing on genetic vaccines.
- To discuss the challenges and requirements for developing effective cancer vaccines.
- To highlight the potential of Adenovirus (Ad)-based vectors and in vivo DNA electroporation (DNA-EP) for cancer vaccination.
Main Methods:
- Review of current literature on cancer vaccine technologies.
- Focus on genetic vaccine approaches, specifically Adenovirus (Ad) vectors and DNA electroporation (DNA-EP).
- Discussion of heterologous prime-boost immunization strategies.
Main Results:
- Genetic vaccines, including Ad vectors and DNA-EP, demonstrate promising immunogenicity for eliciting anti-TAA responses.
- Adenovirus (Ad)-based vectors have achieved immunological proof of concept in humans.
- In vivo electroporation of plasmid DNA (DNA-EP) is a repeatable technology suitable for maintaining anti-tumor immunity.
Conclusions:
- Emerging genetic cancer vaccines, particularly Ad vectors and DNA-EP, offer significant potential for cancer therapy.
- Heterologous prime-boost strategies combining different immunization modalities can induce superior immune responses compared to single-modality vaccines.
- Ad and DNA-EP heterologous prime-boost approaches show promise for enhancing anti-tumor immunity and improving cancer control.
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