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Oncolytic herpes simplex virus immunotherapy for brain tumors: current pitfalls and emerging strategies to overcome therapeutic resistance

Journal

ONCOGENE
Volume 38, Issue 34, Pages 6159-6171

Publisher

SPRINGERNATURE
DOI: 10.1038/s41388-019-0870-y

Keywords

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Funding

  1. Food and Drug Administration Office of Orphan Products Development [R01FD005379]
  2. Department of Defense [W81XWH-15-1-0108]
  3. Rally Foundation for Childhood Cancer Research
  4. Hyundai Hope on Wheels
  5. Kaul Pediatric Research Institute
  6. UAB Medical Scientist Training Program (MSTP)
  7. American Brain Tumor Association
  8. National Cancer Institute of the National Institutes of Health [T32CA183926]
  9. [R01CA217179]

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Malignant tumors of the central nervous system (CNS) continue to be a leading cause of cancer-related mortality in both children and adults. Traditional therapies for malignant brain tumors consist of surgical resection and adjuvant chemoradiation; such approaches are often associated with extreme morbidity. Accordingly, novel, targeted therapeutics for neoplasms of the CNS, such as immunotherapy with oncolytic engineered herpes simplex virus (HSV) therapy, are urgently warranted. Herein, we discuss treatment challenges related to HSV virotherapy delivery, entry, replication, and spread, and in so doing focus on host anti-viral immune responses and the immune microenvironment. Strategies to overcome such challenges including viral re-engineering, modulation of the immunoregulatory microenvironment and combinatorial therapies with virotherapy, such as checkpoint inhibitors, radiation, and vaccination, are also examined in detail.

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