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

Hongbin Wang1,2, Mia Borlongan2, Howard L Kaufman3,4

  • 1Department of Pharmaceutical and Biomedical Sciences, California Northstate University College of Pharmacy, Elk Grove, California, USA.

Insights

Oncolytic viruses, like talimogene laherparepvec, can deliver cytokine payloads to enhance anti-tumor immunity. This review explores various cytokines to optimize oncolytic virus immunotherapy for cancer treatment.

Area of Science:

  • Immunology
  • Virology
  • Oncology

Background:

  • Cytokines are crucial for immune cell regulation and several are approved cancer therapies.
  • Oncolytic viruses directly kill tumor cells and stimulate immune responses against cancer.
  • Talimogene laherparepvec, an oncolytic herpes simplex virus type 1 (oHSV), encodes granulocyte-macrophage colony-stimulating factor (GM-CSF) and is approved for melanoma.

Purpose of the Study:

  • To review the role of cytokine and chemokine payloads in enhancing oncolytic virus (oHSV) antitumor immunity.
  • To discuss preliminary data on various cytokines and chemokines as payloads for oHSV.
  • To explore how optimal cytokine selection can improve clinical outcomes in oncolytic virus immunotherapy.

Main Methods:

  • Review of preliminary data on cytokine and chemokine payloads in oHSV.
  • Analysis of the impact of different cytokines (e.g., GM-CSF, IL-12, IL-15) on antitumor immunity.
  • Examination of cytokine combinations for enhanced therapeutic effects.

Main Results:

  • Oncolytic viruses can effectively deliver therapeutic cytokine payloads to tumor sites.
  • Various cytokines and chemokines, including GM-CSF, IL-12, and IL-15, show potential to enhance oHSV-mediated antitumor immunity.
  • Combinations of cytokines may offer synergistic benefits in driving immune responses.

Conclusions:

  • Cytokine delivery by oHSV is a promising strategy to augment antitumor immunity.
  • Further understanding of optimal cytokine payloads is essential for improving oncolytic virus immunotherapy.
  • Enhanced cytokine payloads can lead to improved clinical benefits for cancer patients treated with oHSV.

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