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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Therapeutic cancer vaccines: reasons to believe
1Epitopea Ltd, Salisbury House, Station Rd, Cambridge CB1 2LA, U.K.
Abstract:
Our hopes of using the power of the immune system to control tumours have been partially fulfilled with anti-PD1 antibodies and other checkpoint inhibitors and the use of engineered T cells targeting lineage-specific surface markers with chimeric antigen receptors. Can these successes be generalised? Therapeutic cancer vaccines aim to educate or re-educate the immune system to recognise tumour specific or tumour associated antigens. After many false dawns, some positive data for the effectiveness of such an approach is starting to emerge in advanced solid tumours, albeit as combination therapies with checkpoint inhibitors. But is the field targeting the right antigens? Interventions using the most effective vaccine platforms to target certain sets of antigens in patients with low disease burden might bring impressive long-term benefits to patients as single agents.
Insights
Cancer vaccines are showing promise, especially in combination with checkpoint inhibitors for advanced solid tumors. Future research should focus on optimal antigen targeting for potential single-agent therapies in low-burden disease.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Current immunotherapies like anti-PD1 antibodies and chimeric antigen receptor T cells show partial success in controlling tumors.
- Therapeutic cancer vaccines aim to harness the immune system against tumor-specific or associated antigens, but have faced challenges.
- Emerging data suggests potential effectiveness of cancer vaccines, particularly in combination with checkpoint inhibitors for advanced solid tumors.
Purpose of the Study:
- To evaluate the potential of therapeutic cancer vaccines in controlling tumors.
- To explore whether current successes in cancer immunotherapy can be generalized to vaccine approaches.
- To investigate the critical role of antigen selection in the efficacy of cancer vaccines.
Main Methods:
- Review of existing data on anti-PD1 antibodies, chimeric antigen receptor T cells, and therapeutic cancer vaccines.
- Analysis of emerging clinical trial data for cancer vaccines in advanced solid tumors.
- Consideration of vaccine platform effectiveness and antigen targeting strategies.
Main Results:
- Positive data is emerging for therapeutic cancer vaccines, particularly as combination therapies with checkpoint inhibitors in advanced solid tumors.
- The effectiveness of cancer vaccines may depend significantly on the specific antigens targeted.
- The field is questioning whether the correct antigens are being pursued for vaccine development.
Conclusions:
- Therapeutic cancer vaccines show emerging promise, especially when combined with checkpoint inhibitors for advanced solid tumors.
- Optimizing antigen selection is crucial for improving vaccine efficacy.
- Targeting specific antigens with effective vaccine platforms in patients with low disease burden may offer significant long-term benefits as monotherapy.
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