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Published on: January 7, 2019
Cancer Vaccines: A Brief Overview
Sunil Thomas1, George C Prendergast2,3,4
1Lankenau Institute for Medical Research, 100 Lancaster Avenue, Wynnewood, PA, 19096, USA.
Abstract:
Vaccine approaches for cancer differ from traditional vaccine approaches for infectious disease in tending to focus on clearing active disease rather than preventing disease. In this review, we provide a brief overview of different types of vaccines and adjuvants that have been investigated for the purpose of controlling cancer burdens in patients, some of which are approved for clinical use or in late-stage clinical trials, such as the personalized dendritic cell vaccine sipuleucel-T (Provenge) and the recombinant viral prostate cancer vaccine PSA-TRICOM (Prostvac-VF). Vaccines against human viruses implicated in the development and progression of certain cancers, such as human papillomavirus in cervical cancer, are not considered here. Cancers express "altered self" antigens that tend to induce weaker responses than the "foreign" antigens expressed by infectious agents. Thus, immune stimulants and adjuvant approaches have been explored widely. Vaccine types considered include autologous patient-derived immune cell vaccines, tumor antigen-expressing recombinant virus vaccines, peptide vaccines, DNA vaccines, and heterologous whole-cell vaccines derived from established human tumor cell lines. Opportunities to develop effective cancer vaccines may benefit from seminal recent advances in understanding how immunosuppressive barricades are erected by tumors to mediate immune escape. In particular, targeted ablation of these barricades with novel agents, such as the immune checkpoint drug ipilimumab (anti-CTLA-4) approved recently for clinical use, may offer significant leverage to vaccinologists seeking to control and prevent malignancy.
Insights
Cancer vaccines aim to clear existing disease, unlike infectious disease vaccines. Novel approaches and immune checkpoint inhibitors show promise for controlling and preventing malignancy by overcoming tumor-induced immune suppression.
Area of Science:
- Oncology
- Immunology
- Vaccinology
Background:
- Cancer vaccines differ from infectious disease vaccines by targeting active disease clearance.
- Tumors present "altered self" antigens, eliciting weaker immune responses than foreign antigens from pathogens.
- Overcoming tumor-induced immunosuppression is crucial for effective cancer immunotherapy.
Purpose of the Study:
- To review various vaccine types and adjuvants investigated for cancer treatment.
- To highlight approved and late-stage clinical trial cancer vaccines.
- To discuss how targeting tumor immunosuppressive mechanisms can enhance vaccine efficacy.
Main Methods:
- Overview of different cancer vaccine modalities.
- Discussion of adjuvants and immune stimulants.
- Exploration of novel therapeutic strategies targeting tumor immune escape.
Main Results:
- Several cancer vaccine types are under investigation, including dendritic cell, viral, peptide, DNA, and whole-cell vaccines.
- Some vaccines, like sipuleucel-T and PSA-TRICOM, are in clinical use or trials.
- Immune checkpoint inhibitors (e.g., ipilimumab) show potential in combination with vaccines.
Conclusions:
- Cancer vaccine development focuses on overcoming the unique challenges of "altered self" antigens and tumor immunosuppression.
- Targeting immunosuppressive barriers erected by tumors is a promising strategy for enhancing cancer vaccine effectiveness.
- Advances in understanding tumor immune escape offer new opportunities for controlling and preventing malignancy through vaccination.
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