Oncolytic Adenoviruses: The Cold War against Cancer Finally Turns Hot.
Bryan OronskyBrian GastmanAnthony P ConleyChristopher ReidScott CaroenTony ReidPublished in: Cancers (2022)
Oncolytic viruses, colloquially referred to as "living drugs", amplify themselves and the therapeutic transgenes that they carry to stimulate an immune response both locally and systemically. Remarkable exceptions aside, such as the recent 14-patient trial with the PD-1 inhibitor, dostarlimab, in mismatch repair (MMR) deficient rectal cancer, where the complete response rate was 100%, checkpoint inhibitors are not cure-alls, which suggests the need for a combination partner like oncolytic viruses to prime and augment their activity. This review focuses on adenoviruses, the most clinically investigated of all the oncolytic viruses. It covers specific design features of clinical adenoviral candidates and highlights their potential both alone and in combination with checkpoint inhibitors in clinical trials to turn immunologically "cold" and unresponsive tumors into "hotter" and more responsive ones through a domino effect. Finally, a "mix-and-match" combination of therapies based on the paradigm of the cancer-immunity cycle is proposed to augment the immune responses of oncolytic adenoviruses.
Keyphrases
- immune response
- clinical trial
- papillary thyroid
- dna damage
- rectal cancer
- squamous cell
- cell cycle
- toll like receptor
- squamous cell carcinoma
- dendritic cells
- case report
- study protocol
- lymph node metastasis
- phase iii
- oxidative stress
- randomized controlled trial
- inflammatory response
- cell proliferation
- sensitive detection
- genetic diversity
- human immunodeficiency virus
- living cells
- hepatitis c virus
- quantum dots
- hiv testing
- antiretroviral therapy
- single molecule