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Updated: May 15, 2026

Monitoring Functionality and Morphology of Vasculature Recruited by Factors Secreted by Fast-growing Tumor-generating Cells
Published on: November 23, 2014
Modulation of immunity by antiangiogenic molecules in cancer
Magali Terme1, Orianne Colussi, Elie Marcheteau
1INSERM U970, Paris Cardiovascular Research Center, Université Paris-Descartes, Sorbonne Paris Cité, 56 rue Leblanc, 75015 Paris, France.
Abstract:
In the last decades a new class of therapeutic drugs have been developed that block tumor angiogenesis. These antiangiogenic molecules, which target VEGF or VEGFR, PDGFR, and c-kit, can act not only on endothelial cells but also on immune cells. Some antiangiogenic molecules inhibit the development of immunosuppressive mechanisms developed by the tumors to escape the immune system (such as regulatory T cells, myeloid-derived suppressor cells, and immunosuppressive cytokines). These immunomodulatory effects must be characterized in detail to enable a better prescription of these treatments. In this paper we will focus on the impact of anti-angiogenic drugs on immunosuppression and their potential combination with immunotherapeutic strategies. Interestingly, immune parameters or their modulation during treatment could serve as potential biomarkers of response or resistance to anti-angiogenic therapies.
Insights
Anti-angiogenic drugs targeting tumor blood vessel growth also impact immune cells, potentially reversing tumor-induced immunosuppression. Understanding these effects is key for combining anti-angiogenic therapies with immunotherapy and identifying treatment response biomarkers.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Tumor angiogenesis is a key process targeted by new therapeutic drugs.
- Anti-angiogenic molecules targeting VEGF, VEGFR, PDGFR, and c-kit impact both endothelial and immune cells.
- Tumors develop immunosuppressive mechanisms to evade the immune system, involving regulatory T cells, myeloid-derived suppressor cells, and cytokines.
Purpose of the Study:
- To detail the immunomodulatory effects of anti-angiogenic drugs.
- To explore the potential of combining anti-angiogenic therapies with immunotherapeutic strategies.
- To identify immune parameters as potential biomarkers for anti-angiogenic therapy response.
Main Methods:
- Review of existing literature on anti-angiogenic drugs and their effects on the tumor microenvironment.
- Analysis of immunomodulatory mechanisms affected by anti-angiogenic agents.
- Discussion of potential combination strategies with immunotherapy.
Main Results:
- Anti-angiogenic drugs can inhibit tumor-induced immunosuppression by affecting regulatory T cells, myeloid-derived suppressor cells, and immunosuppressive cytokines.
- These drugs can modulate immune cell function, potentially enhancing anti-tumor immunity.
- Immune parameters may serve as predictive biomarkers for response or resistance to anti-angiogenic therapies.
Conclusions:
- Anti-angiogenic drugs possess significant immunomodulatory properties that can counteract tumor immunosuppression.
- Combination of anti-angiogenic drugs with immunotherapy holds promise for improved cancer treatment outcomes.
- Monitoring immune parameters during treatment can guide therapeutic decisions and predict patient response.
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