During the last thirty years I have been working in cancer research, focused on the development of immunotherapeutic agents, such as MAbs and vaccines for the treatment of different types of cancer. I believe that tumor immunotherapy could only be successful if we trigger multiple checkpoints in the immune system, instructing it to see "cancer cells" as "viral-infected-cells", therefore leading to more effective antitumor immune responses. Specifically, my goals include the development and characterization of new MAbs raised against key molecules of the immune system, such as co-stimulatory and co-inhibitory molecules, thus activating or blocking their function when affects the anti-tumor response we desire to obtain. Another goal of my career is to assist other investigators, users of the MAF, with their own research projects, providing them my expertise and advise and developing the MAbs they need for their basic, translational and clinical research. Examples of successful antibodies developed at the Core are the anti-human OX40 antibody that blocks the function of inducible and natural Tregs (I am patent co-author) and the anti - PR1/ HLA-A2, a T cell receptor-like antibody that mediates complement dependent cytotoxicity against acute myeloid leukemia progenitor cells. Both of them are under clinical development.
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Professor, Director of Monoclonal Antibodies Core Facility
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