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Targeting VEGF/VEGFR to Modulate Antitumor Immunity

Frontiers in Immunology · 2018 · Vol. 9 · pp. 978–978
Ju YangJing YanBaorui Liu

Abstract

In addition to the crucial role in promoting the growth of tumor vessels, vascular endothelial growth factor (VEGF) is also immunosuppressive. VEGF can inhibit the function of T cells, increase the recruitment of regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs), and hinder the differentiation and activation of dendritic cells (DCs). Recent studies have investigated the role of antiangiogenic agents in antitumor immunity, especially in recent 3 years. Therefore, it is necessary to update the role of targeting VEGF/VEGFR in antitumor immunity. In this review, we focus on the latest clinical and preclinical findings on the modulatory role of antiangiogenic agents targeting VEGF/VEGFR in immune cells, including effector T cells, Tregs, MDSCs, DCs, tumor-associated macrophages, and mast cells. Our review will be potentially helpful for the development of combinations of angiogenesis inhibitors with immunological modulators.

Immune cells in cancerAngiogenesis and VEGF in CancerCancer Immunotherapy and BiomarkersAngiogenesisImmune systemMyeloid-derived Suppressor CellCancer researchVascular endothelial growth factorImmunologyVEGF receptorsImmunityEffectorMedicine

MeSH terms

Myeloid-Derived Suppressor CellsAnimalsCell DifferentiationDendritic CellsHumansImmunologic FactorsNeoplasmsNeovascularization, PathologicAngiogenesis InhibitorsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth FactorsT-Lymphocytes, RegulatoryMice

Funding

  • National Natural Science Foundation of China
  • Government of Jiangsu Province
  • Natural Science Foundation of Jiangsu Province
  • National Key Research and Development Program of China
Citations
613
FWCI
21.77
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References
118
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100%
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