Abstract | BACKGROUND: Signaling through VEGF/VEGFR induces cancer angiogenesis and affects immune cells. An increasing number of studies have recently focused on combining anti- VEGF/VEGFR agents and immune checkpoint inhibitors (ICIs) to treat cancer in preclinical and clinical settings. BD0801 is a humanized rabbit anti- VEGF monoclonal antibody in the clinical development stage. METHODS: In this study, the anti- cancer activities of BD0801 and its potential synergistic anti- tumor effects when combined with different immunotherapies were assessed by using in vitro assays and in vivo tumor models. Ex vivo studies were conducted to reveal the possible mechanisms of actions (MOA) underlying the tumor microenvironment modification. RESULTS: BD0801 showed more potent antitumor activity than bevacizumab, reflected by stronger blockade of VEGF/VEGFR binding and enhanced inhibitory effects on human umbilical vein endothelial cells (HUVECs). BD0801 exhibited dose-dependent tumor growth inhibitory activities in xenograft and murine syngeneic tumor models. Notably, combining BD0801 with either anti-PD-1 or anti-PD-L1 antibodies showed synergistic antitumor efficacy in both lung and colorectal cancer mouse models. Furthermore, the mechanistic studies suggested that the MOA of the antitumor synergy involves improved tumor vasculature normalization and enhanced T-cell mediated immunity, including increased tumor infiltration of CD8+ and CD4+ T cells and reduced double-positive CD8+PD-1+ T cells. CONCLUSIONS:
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Authors | Liting Xue, Xingyuan Gao, Haoyu Zhang, Jianxing Tang, Qian Wang, Feng Li, Xinxin Li, Xiaohong Yu, Zhihong Lu, Yue Huang, Renhong Tang, Wenqing Yang |
Journal | BMC cancer
(BMC Cancer)
Vol. 21
Issue 1
Pg. 1134
(Oct 22 2021)
ISSN: 1471-2407 [Electronic] England |
PMID | 34686154
(Publication Type: Journal Article)
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Copyright | © 2021. The Author(s). |
Chemical References |
- Angiogenesis Inhibitors
- Immune Checkpoint Inhibitors
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Topics |
- Angiogenesis Inhibitors
(pharmacology, therapeutic use)
- Animals
- Disease Models, Animal
- Female
- Humans
- Immune Checkpoint Inhibitors
(pharmacology, therapeutic use)
- Mice
- Tumor Microenvironment
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