Target intelligence / Profile preview

Herpes simplex virus type 1 (oncolytic) (oHSV-1 (or oHSV, when referring to the platform generally))

Target
oHSV-1 (or oHSV, when referring to the platform generally)
Molecular classification
Other (oncolytic virus; gene therapy agent; viral vector)
01

Overview

Oncolytic herpes simplex virus therapy utilizes modified HSV, typically HSV-1, for direct tumor cell lysis and induction of anti-tumor immune responses. The virus is engineered to preferentially replicate in cancer cells—often through deletion of virulence genes or insertion of immune-stimulating factors—triggering lytic cell death and the release of tumor antigens that prime immune responses[1][2][4]. Anti-HSV antivirals like acyclovir can be used as an added safety measure. FDA-approved agents such as talimogene laherparepvec (T-VEC) are examples of this approach, notably for advanced melanoma.

Other names
oncolytic herpes simplex virusoHSVherpes simplex virus-mediated oncolytic therapyHSV-mediated oncolytic virotherapy
02

Mechanism of action

- Selective infection and lysis of tumor cells (oncolysis) - Stimulation of anti-tumor immune response via release of tumor-associated and viral antigens - Induction of immunogenic cell death and maturation of dendritic cells - Enhanced antigen presentation leading to T cell activation

03

Biological functions

Cell deathImmune responseCell lysisInduction of immunogenic cell deathViral replicationAntigen release
04

Disease associations

CancerInfection
05

Safety considerations

Potential for encephalitis (particularly with wild-type HSV)systemic viral spread in immunocompromised hostspre-existing anti-HSV immunityoff-target infectionviral reactivationinflammatory toxicitiesantiviral resistance
06

Interacting drugs

Talimogene laherparepvec (T-VEC; a genetically modified HSV-1)

2 more in the full profile.

07

Biomarkers

Tumor-associated antigensviral DNA in plasmaimmune cell infiltration (CD8+ T cells)released DAMPs (e.g. HMGB1, ATP, calreticulin exposure)

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