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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Prostate cancer vaccines: maximizing a suboptimal immune response for improved outcome
1Genitourinary Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA. slovins@mskcc.org
Abstract:
As approaches toward isolating tumor-associated antigens have become more refined, vaccines composed of novel cell surface proteins, peptides, or DNA encoding the molecule of interest have been developed. All of these approaches have in some way been shown to break immunologic tolerance, either by the generation of high-titer antibodies against the immunogen or by eliciting T-cell responses as shown by T-cell proliferation assays or specific cytokine release via enzyme-linked immunosorbent spot. No single immunologic approach to date has successfully shown significant durable disease remission in prostate cancer, albeit clinical trials using immune modulators together with vaccines have suggested that radiographic antitumor responses are feasible. This review updates the status of prostate cancer vaccines as tools for induction of active immunity and discusses the issues relevant to their clinical trial development.
Insights
Prostate cancer vaccines targeting tumor antigens show promise in breaking immunologic tolerance and eliciting immune responses. While durable remission remains elusive, clinical trials suggest feasibility of radiographic antitumor responses.
Area of Science:
- Oncology
- Immunology
- Vaccine Development
Background:
- Advances in isolating tumor-associated antigens have enabled development of novel prostate cancer vaccines.
- Vaccine strategies include cell surface proteins, peptides, and DNA encoding target antigens.
- These approaches aim to overcome immune tolerance in cancer patients.
Purpose of the Study:
- To review the current status of prostate cancer vaccines for active immunotherapy.
- To discuss challenges and considerations for clinical trial development of these vaccines.
Main Methods:
- Review of scientific literature on prostate cancer vaccines and immunotherapy.
- Analysis of immune responses, including antibody generation and T-cell activation (proliferation, cytokine release).
- Evaluation of clinical trial data on vaccine efficacy and safety.
Main Results:
- Prostate cancer vaccines have demonstrated the ability to break immunologic tolerance.
- Immune responses observed include high-titer antibodies and T-cell activation.
- Clinical trials combining vaccines with immunomodulators suggest feasibility of radiographic antitumor responses.
Conclusions:
- Prostate cancer vaccines are valuable tools for inducing active immunity.
- Significant durable disease remission has not yet been achieved with monotherapy vaccines.
- Further development and clinical trials are necessary to optimize vaccine strategies for prostate cancer treatment.
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