Abstract
Cancer vaccines, in order to be successful, must generate tumor-specific CD8+ T cells that can effectively traffic to the tumor microenvironment (TME) and maintain their activity in the immunosuppressive TME. T cell avidity and priming are critical components of an effective vaccine response, but the immunosuppressive environment of the tumor may still inhibit optimal T cell function. The addition of immune checkpoint inhibitors to existing cancer vaccines has been associated with an effective T cell response that translates into prolonged survival. This article will examine the components necessary to induce a potent and effective CD8+ T cell response using combination vaccine immunotherapies.
Original language | English (US) |
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Title of host publication | Immunity to Pathogens and Tumors |
Publisher | Elsevier Inc. |
Pages | 534-541 |
Number of pages | 8 |
Volume | 4 |
ISBN (Print) | 9780080921525 |
DOIs | |
State | Published - Apr 27 2016 |
Keywords
- Avidity
- CD8 T cells
- CTLA-4
- Cyclophosphamide
- GVAX
- Immune checkpoint inhibitor
- Immunotherapy
- Listeria monocytogenes
- OX40
- PD-1
- Tumor microenvironment
- Vaccines
ASJC Scopus subject areas
- General Medicine