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Tumor cell lysis via herpes simplex virus type 1 replication exploits the ability of engineered or wild-type HSV-1 viruses to selectively infect and destroy cancerous tissues by hijacking cellular processes for robust viral propagation. This approach forms the foundation for modern oncolytic virotherapies such as T-VEC that combine direct cytolytic effects with stimulation of systemic anti-tumoral immunity.
Selective replication within tumor cells leading to cell lysis and release of tumor antigens, stimulating anti-tumor immune responses.
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