Target intelligence / Profile preview

Oncolytic viral therapy (OVT)

Target
OVT
Molecular classification
Biological therapy, Gene therapy, Immunotherapy
01

Overview

Oncolytic viral therapy is a promising treatment modality that uses replication-competent lytic viruses to selectively target and destroy tumor cells while sparing normal cells. These viruses can be naturally occurring or genetically engineered to enhance their tumor selectivity and oncolytic activity. The selectivity is achieved through various mechanisms, including exploitation of defective interferon signaling pathways in tumor cells, modification of viral coat proteins to target tumor-specific receptors, and placing essential viral genes under the control of tumor-specific promoters. Oncolytic viruses mediate tumor cell destruction through two main mechanisms: direct lysis of infected cells and indirect augmentation of host antitumor immunity. The viruses can also be armed with therapeutic transgenes to enhance their efficacy. This approach offers a unique opportunity for tumor targeting with reduced side effects compared to conventional chemotherapy and radiotherapy.

Other names
Viral oncotherapyOncolytic virotherapyOncolytic viral therapyTumor-selective viral therapy
02

Mechanism of action

Direct oncolysis of infected tumor cells Exploitation of defective interferon signaling pathways in tumor cells Targeting of tumor-specific receptors or molecular pathways Stimulation of systemic antitumor immune responses Induction of immunogenic cell death

03

Biological functions

Direct tumor cell lysisInduction of apoptosisStimulation of antitumor immune responsesTumor microenvironment modification
04

Disease associations

CancerMalignant tumors
05

Safety considerations

Off-target viral replication in immunocompromised patientsPotential systemic toxicityNeutralizing antibody developmentLimited viral distribution and penetration in solid tumorsViral clearance by host immune system
06

Interacting drugs

Engineered oncolytic viruses (HSV-1, adenovirus, vesicular stomatitis virus, Newcastle disease virus, reovirus)

1 more in the full profile.

07

Biomarkers

Defects in interferon signaling pathwaysOverexpression of specific tumor receptors (e.g., CEA)Defects in Rb pathwaySurvivin overexpressionTumor-specific promoter activity

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