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Authors
Supervisors
Lucas, Sophie
Abstract
Cancer immunotherapies, such as monoclonal antibodies (mAbs) directed against PD-1, aim at boosting immune responses against tumor cells. They have become a standard of care for several types of cancer. However, a majority of patients do not respond to current immunotherapies. Resistance to PD-1 blockade can in part be explained by the action of TGF-b1, an immunosuppressive cytokine activated notably by regulatory T cells (Tregs) via a mechanism that requires protein GARP. We developed antibodies against GARP:TGF-b1 complexes that block TGF-b1 activation by Tregs and we evaluated their anti-tumor efficacy in tumor-bearing mice. We observed that anti-GARP:TGF-b1 mAbs induce the regression of tumors otherwise resistant to anti-PD-1, and we showed that combined blockade of GARP:TGF-b1 and PD-1 can exert anti-tumor activity via multiple modes of action. This may prove important for the selection of cancer patients who could benefit from this novel form of immunotherapy in the clinics.
Affiliations

Citations

Bertrand Van Ouytsel, S.-C. (2021). Multiple modes of action for antibodies targeting GARP-expressing cells in tumors. https://hdl.handle.net/2078.5/114056