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Updated: Jul 5, 2026

Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Anti-angiogenesis: making the tumor vulnerable to the immune system
1Department of Pathology, Research Institute for Growth and Development (GROW), University Hospital Maastricht, AZ Maastricht, The Netherlands. aw.griffioen@path.unimaas.nl
Abstract:
Ongoing angiogenesis has been shown to possess immune suppressive activity through several mechanisms. One of these mechanisms is the suppression of adhesion receptors, such as intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and E-selectin-adhesion molecules involved in leukocyte interactions-on the vascular endothelium. This phenomenon, when happening to the tumor endothelium, supports tumor growth due to escape from immunity. Since angiogenesis has this immune suppressive effect, it has been hypothesized that inhibition of angiogenesis may circumvent this problem. In vitro and in vivo data now show that several angiogenesis inhibitors are able to normalize endothelial adhesion molecule expression in tumor blood vessels, restore leukocyte vessel wall interactions, and enhance the inflammatory infiltrate in tumors. It is suggested that such angiogenesis inhibitors can make tumors more vulnerable for the immune system and may therefore be applied to facilitate immunotherapy approaches for the treatment of cancer.
Insights
Ongoing angiogenesis suppresses the immune system by reducing leukocyte interactions. Inhibiting angiogenesis can restore these interactions, making tumors more vulnerable to immune attack and enhancing cancer immunotherapy.
Area of Science:
- Immunology
- Oncology
- Vascular Biology
Background:
- Ongoing angiogenesis contributes to immune suppression via mechanisms like reduced adhesion molecule expression on vascular endothelium.
- Tumor endothelium's altered adhesion molecules facilitate immune evasion and support tumor growth.
- Angiogenesis inhibition is hypothesized to counteract this immune suppressive effect.
Purpose of the Study:
- To investigate whether inhibiting angiogenesis can restore immune cell interactions with tumor vasculature.
- To determine if angiogenesis inhibitors can enhance anti-tumor immunity and facilitate immunotherapy.
Main Methods:
- In vitro and in vivo studies were conducted.
- The effects of various angiogenesis inhibitors on endothelial adhesion molecule expression were assessed.
- Leukocyte-endothelium interactions and inflammatory infiltrate in tumors were analyzed.
Main Results:
- Angiogenesis inhibitors normalized endothelial adhesion molecule expression in tumor blood vessels.
- Restoration of leukocyte-vessel wall interactions was observed.
- Enhanced inflammatory infiltrate within tumors was detected.
Conclusions:
- Inhibition of angiogenesis can reverse immune suppressive effects associated with tumor vasculature.
- Angiogenesis inhibitors may re-sensitize tumors to the immune system.
- These inhibitors show potential as adjuncts to facilitate cancer immunotherapy approaches.
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