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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Active specific immunotherapy targeting the Wilms' tumor protein 1 (WT1) for patients with hematological malignancies
Ann Van Driessche1, Zwi N Berneman, Viggo F I Van Tendeloo
1Laboratory of Experimental Hematology, Vaccine & Infectious Disease Institute (VaxInfectio), Faculty of Medicine, University of Antwerp, Antwerp, Belgium. ann.van.driessche@uza.be
Abstract:
There is a growing body of evidence that Wilms' tumor protein 1 (WT1) is a promising tumor antigen for the development of a novel class of universal cancer vaccines. Recently, in a National Cancer Institute prioritization project, WT1 was ranked first in a list of 75 cancer antigens. In this light, we exhaustively reviewed all published cancer vaccine trials reporting on WT1-targeted active specific immunotherapy in patients with hematological malignancies and solid tumors. In all clinical trials, vaccine-induced immunological responses could be detected. Importantly, objective clinical responses (including stable disease) were observed in 46% and 64% of evaluable vaccinated patients with solid tumors and hematological malignancies, respectively. Immunogenicity of WT1-based cancer vaccines was demonstrated by the detection of a specific immunological response in 35% and 68% of evaluable patients with solid tumors and hematological malignancies, respectively. In order to become part of the armamentarium of the modern oncologist, it will be important to design WT1-based immunotherapies applicable to a large patient population, to standardize vaccination protocols enabling systematic review, and to further optimize the immunostimulatory capacity of the vaccine components. Moreover, improved immunomonitoring tools that reveal clinically relevant T-cell responses will further shape the ideal WT1 immunotherapy strategy. In conclusion, the clinical results obtained so far in WT1-targeted cancer vaccine trials reveal an untapped potential for inducing cancer immunity with minimal side effects and hold promise for a new adjuvant treatment against residual disease and against cancer relapse.
Insights
Wilms' tumor protein 1 (WT1) cancer vaccines show promise, inducing immune responses and clinical benefits in patients with hematological malignancies and solid tumors. Further optimization is needed for broader application in cancer treatment.
Area of Science:
- Oncology
- Immunology
- Vaccine Development
Background:
- Wilms' tumor protein 1 (WT1) is recognized as a significant tumor antigen.
- WT1 was prioritized as a top cancer antigen by the National Cancer Institute.
- WT1-targeted active specific immunotherapy represents a novel approach to cancer vaccination.
Purpose of the Study:
- To review published cancer vaccine trials targeting WT1.
- To evaluate the efficacy and immunogenicity of WT1-based immunotherapies.
- To identify areas for improvement in WT1-targeted cancer vaccine development.
Main Methods:
- Systematic review of published clinical trials on WT1-targeted cancer vaccines.
- Analysis of immunological and clinical response data from patients with hematological malignancies and solid tumors.
- Assessment of vaccine-induced immune responses and objective clinical outcomes.
Main Results:
- All reviewed trials detected vaccine-induced immunological responses.
- Objective clinical responses (including stable disease) were observed in 46% of solid tumor patients and 64% of hematological malignancy patients.
- Immunogenicity was demonstrated in 35% of solid tumor patients and 68% of hematological malignancy patients.
Conclusions:
- WT1-based cancer vaccines demonstrate potential for inducing anti-cancer immunity with minimal side effects.
- Further research should focus on large-scale applicability, standardized protocols, and enhanced vaccine components.
- Improved immunomonitoring is crucial for optimizing WT1 immunotherapy strategies and adjuvant treatment against residual disease or relapse.
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