4.8 Article

Vascular Normalization as an Emerging Strategy to Enhance Cancer Immunotherapy

Journal

CANCER RESEARCH
Volume 73, Issue 10, Pages 2943-2948

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-12-4354

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Funding

  1. Medimmune
  2. Roche
  3. NIH [P01-CA080124, R01-CA115767, R01-CA085140, R01-CA126642, R21-CA139168, R01-CA159258, R01-CA096915]
  4. Federal Share/NCI Proton Beam Program
  5. Department of Defense [W81XWH-10-1-0016]
  6. Postdoctoral Research Fellowship [W81XWH-11-1-0619]
  7. American Cancer Society [RSG-11-073-01-TBG]
  8. National Foundation for Cancer Research
  9. Australian-American Fulbright Commission
  10. American Society of Clinical Oncology

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The recent approval of Provenge has brought new hope for anticancer vaccine therapies. However, the immunosuppressive tumor microenvironment seems to impair the efficacy of vaccine therapies. The abnormal tumor vasculature creates a hypoxic microenvironment that polarizes inflammatory cells toward immune suppression. Moreover, tumors systemically alter immune cells' proliferation, differentiation, and function via secretion of growth factors and cytokines. For example, VEGF, a major proangiogenic cytokine induced by hypoxia, plays a critical role in immunosuppression via these mechanisms. Hence, antiangiogenic treatment may be an effective modality to potentiate immunotherapy. Here, we discuss the local and systemic effects of VEGF on tumor immunity and propose a potentially translatable strategy to re-engineer the tumor-immune microenvironment and improve cancer immunotherapy by using lower vascular normalizing doses of antiangiogenic agents. Cancer Res; 73(10); 2943-8. (C) 2013 AACR.

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