Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?

Cytokines are small proteins that regulate the growth and functional activity of immune cells, and several have been approved for cancer therapy. Oncolytic viruses are agents that mediate antitumor activity by directly killing tumor cells and inducing immune responses. Talimogene laherparepvec is an...

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Main Authors: Howard L Kaufman, Hongbin Wang, Dipongkor Saha, Samuel D Rabkin, Mia Borlongan, Uyen Le, Hans J Nauwynck
Format: Article
Language:English
Published: BMJ Publishing Group 2024-05-01
Series:Journal for ImmunoTherapy of Cancer
Online Access:https://jitc.bmj.com/content/12/5/e008025.full
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author Howard L Kaufman
Hongbin Wang
Dipongkor Saha
Samuel D Rabkin
Mia Borlongan
Uyen Le
Hans J Nauwynck
author_facet Howard L Kaufman
Hongbin Wang
Dipongkor Saha
Samuel D Rabkin
Mia Borlongan
Uyen Le
Hans J Nauwynck
author_sort Howard L Kaufman
collection DOAJ
description Cytokines are small proteins that regulate the growth and functional activity of immune cells, and several have been approved for cancer therapy. Oncolytic viruses are agents that mediate antitumor activity by directly killing tumor cells and inducing immune responses. Talimogene laherparepvec is an oncolytic herpes simplex virus type 1 (oHSV), approved for the treatment of recurrent melanoma, and the virus encodes the human cytokine, granulocyte-macrophage colony-stimulating factor (GM-CSF). A significant advantage of oncolytic viruses is the ability to deliver therapeutic payloads to the tumor site that can help drive antitumor immunity. While cytokines are especially interesting as payloads, the optimal cytokine(s) used in oncolytic viruses remains controversial. In this review, we highlight preliminary data with several cytokines and chemokines, including GM-CSF, interleukin 12, FMS-like tyrosine kinase 3 ligand, tumor necrosis factor α, interleukin 2, interleukin 15, interleukin 18, chemokine (C-C motif) ligand 2, chemokine (C-C motif) ligand 5, chemokine (C-X-C motif) ligand 4, or their combinations, and show how these payloads can further enhance the antitumor immunity of oHSV. A better understanding of cytokine delivery by oHSV can help improve clinical benefit from oncolytic virus immunotherapy in patients with cancer.
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issn 2051-1426
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series Journal for ImmunoTherapy of Cancer
spelling doaj-art-ae1324671e874fbf8b0558f501e18cfa2025-02-10T04:55:09ZengBMJ Publishing GroupJournal for ImmunoTherapy of Cancer2051-14262024-05-0112510.1136/jitc-2023-008025Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?Howard L Kaufman0Hongbin Wang1Dipongkor Saha2Samuel D Rabkin3Mia Borlongan4Uyen Le5Hans J Nauwynck66Ankyra Therapeutics/Massachusetts General Hospital, Boston, MA, USADepartment of Pharmaceutical and Biomedical Sciences, California Northstate University College of Pharmacy, Elk Grove, California, USADepartment of Pharmaceutical and Biomedical Sciences, California Northstate University College of Pharmacy, Elk Grove, California, USABrain Tumor Research Center, Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USACollege of Graduate Studies, California Northstate University, Elk Grove, California, USADepartment of Pharmaceutical and Biomedical Sciences, California Northstate University College of Pharmacy, Elk Grove, California, USALaboratory of Virology, Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Merelbeke, BelgiumCytokines are small proteins that regulate the growth and functional activity of immune cells, and several have been approved for cancer therapy. Oncolytic viruses are agents that mediate antitumor activity by directly killing tumor cells and inducing immune responses. Talimogene laherparepvec is an oncolytic herpes simplex virus type 1 (oHSV), approved for the treatment of recurrent melanoma, and the virus encodes the human cytokine, granulocyte-macrophage colony-stimulating factor (GM-CSF). A significant advantage of oncolytic viruses is the ability to deliver therapeutic payloads to the tumor site that can help drive antitumor immunity. While cytokines are especially interesting as payloads, the optimal cytokine(s) used in oncolytic viruses remains controversial. In this review, we highlight preliminary data with several cytokines and chemokines, including GM-CSF, interleukin 12, FMS-like tyrosine kinase 3 ligand, tumor necrosis factor α, interleukin 2, interleukin 15, interleukin 18, chemokine (C-C motif) ligand 2, chemokine (C-C motif) ligand 5, chemokine (C-X-C motif) ligand 4, or their combinations, and show how these payloads can further enhance the antitumor immunity of oHSV. A better understanding of cytokine delivery by oHSV can help improve clinical benefit from oncolytic virus immunotherapy in patients with cancer.https://jitc.bmj.com/content/12/5/e008025.full
spellingShingle Howard L Kaufman
Hongbin Wang
Dipongkor Saha
Samuel D Rabkin
Mia Borlongan
Uyen Le
Hans J Nauwynck
Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
Journal for ImmunoTherapy of Cancer
title Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
title_full Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
title_fullStr Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
title_full_unstemmed Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
title_short Cytokine-armed oncolytic herpes simplex viruses: a game-changer in cancer immunotherapy?
title_sort cytokine armed oncolytic herpes simplex viruses a game changer in cancer immunotherapy
url https://jitc.bmj.com/content/12/5/e008025.full
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