Target intelligence / Profile preview

Herpes simplex virus type 1 (oncolytic variant) (HSV-1 (oncolytic))

Target
HSV-1 (oncolytic)
Molecular classification
Virus, Oncolytic virus, Replication-competent virus
01

Overview

Oncolytic herpes simplex virus type 1 (HSV-1) is a genetically engineered virus used as a therapeutic agent in cancer treatment. Upon direct injection or intratumoral replication, the virus selectively infects and destroys tumor cells through lytic replication, sparing normal tissue due to engineered attenuations. The destruction of tumor cells releases immunogenic molecules that promote dendritic cell maturation and stimulate the activation of cytotoxic T cells, resulting in a robust antitumor immune response. These mechanisms combine direct oncolysis with systemic cancer immunotherapy, particularly for solid tumors. Several engineered variants express immune-stimulating transgenes, such as GM-CSF, anti-PD-1 antibody, or cytokines, to further augment antitumor efficacy[1][2][3][4].

Other names
Oncolytic HSV-1oHSV-1Oncolytic herpes simplex virus 1HSV-1-based oncolytic virusTalimogene laherparepvec (T-VEC)
02

Mechanism of action

Selective replication in tumor cells (lytic cycle) Direct tumor cell lysis Release of danger signals (ATP, HMGB1, calreticulin) triggering dendritic cell activation and cross-presentation to T cells Promotes antitumor innate and adaptive immune responses

03

Biological functions

Cell lysisImmunogenic cell deathActivation of innate and adaptive immune responseTumor cell killingInduction of apoptosis
04

Disease associations

Cancer (multiple tumor types, especially melanoma, glioma, colon adenocarcinoma)
05

Safety considerations

Potential for local and systemic inflammation (e.g. GM-CSF effects: fever, fatigue)Risk of unintended viral infection (controllable with antivirals)Necessity for repeated dosing (limited duration of therapeutic effect)
06

Interacting drugs

Talimogene laherparepvec (T-VEC)

2 more in the full profile.

07

Biomarkers

Damage-associated molecular patterns (DAMPs): HMGB1, ATP, calreticulin exposureIncreased dendritic cell infiltrationCytotoxic T lymphocyte (CD8+) activity

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