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Updated: Jun 2, 2026

Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
Published on: July 20, 2019
A novel antiangiogenic and vascular normalization therapy targeted against human CD160 receptor
Sophie Chabot1, Nabila Jabrane-Ferrat, Karine Bigot
1Institut National de la Santé et de la Recherche Médicale U1043, F-31300 Toulouse, France.
Abstract:
Angiogenesis plays an essential role in several diseases of the eye and in the growth of solid tumors, but existing antiangiogenic therapies have limited benefits in several cases. We report the antiangiogenic effects of a monoclonal antibody, CL1-R2, in several animal models of neovascularization. CL1-R2 recognizes human CD160, a membrane receptor which is conserved in various mammal species. We show that CD160 is expressed on the endothelial cells of newly formed blood vessels in human colon carcinoma and mouse B16 melanoma but not in vessels of healthy tissues. CL1-R2 reduced fibroblast growth factor 2-induced neovascularization in the rabbit cornea, in a mouse model of oxygen-induced retinopathy, and in a mouse Matrigel plug assay. Treatment of B16 melanoma-bearing mice with CL1-R2 combined with cyclophosphamide chemotherapy caused regression of the tumor vasculature and normalization of the remaining vessels as shown by Doppler ultrasonography, intravital microscopy, and histology. These studies validate CD160 as a potential new target in cases of human pathological ocular and tumor neoangiogenesis that do not respond or become resistant to existing antiangiogenic drugs.
Insights
A new monoclonal antibody, CL1-R2, targets CD160, effectively inhibiting pathological angiogenesis in eye diseases and tumors. This offers a promising new therapeutic avenue for resistant or unresponsive cases.
Area of Science:
- Oncology
- Ophthalmology
- Immunology
Background:
- Angiogenesis is crucial in ocular diseases and tumor growth.
- Current antiangiogenic therapies have limitations in efficacy.
- Pathological neovascularization requires novel therapeutic targets.
Purpose of the Study:
- To investigate the antiangiogenic effects of monoclonal antibody CL1-R2.
- To evaluate CL1-R2 as a potential therapeutic target for CD160.
- To assess CL1-R2 efficacy in preclinical models of neovascularization.
Main Methods:
- CL1-R2 was tested in rabbit cornea, mouse oxygen-induced retinopathy, and Matrigel plug assays.
- CD160 expression was analyzed in tumor vasculature and healthy tissues.
- CL1-R2 efficacy was assessed in combination with chemotherapy in melanoma models.
Main Results:
- CL1-R2 targets CD160, expressed on neovascular endothelial cells but not in healthy tissues.
- CL1-R2 demonstrated significant antiangiogenic effects in multiple preclinical models.
- Combination therapy with CL1-R2 and chemotherapy regressed tumor vasculature and normalized remaining vessels.
Conclusions:
- CD160 is a validated target for inhibiting pathological angiogenesis.
- CL1-R2 shows potential as a novel therapeutic agent for resistant ocular and tumor neovascularization.
- CL1-R2 offers a new strategy for treating angiogenesis-dependent diseases.
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