Adoptive cell therapy (ACT) is poised to expand the curative potential of immunotherapy. ACT works by administering T cells that have been genetically engineered to express tumor-specific T cell receptors (TCRs) so that they recognize a particular cancer antigen. Dr. Gormally’s [Dennis and Marsha Dammerman Fellow] work addresses two major challenges that currently limit the effectiveness of ACTs against solid tumors: identifying antigen targets that can be recognized by the immune system, and designing TCRs that target those antigens with exquisite specificity. Dr. Gormally and his colleagues have identified multiple immunogenic antigens derived from cancer-causing mutations and developed a powerful approach to retrieve potent, antigen-specific TCRs from large libraries of blood samples from cancer patients. The goal of these efforts is to identify safe and effective TCRs for clinical application. Dr. Gormally received his PhD from the University of Cambridge, Cambridge, his MD from Yale School of Medicine, New Haven, and his BA from Pomona College, Claremont.
Damon Runyon Researchers
Meet Our Scientists
Michael V. Gormally, MD, PhD
      Project title:     "Immunologic targeting of 'undruggable' TP53 hotspot mutations through T cell receptor gene therapy"  
  
      Institution:     Memorial Sloan Kettering Cancer Center  
  
      Named Award:     Dennis and Marsha Dammerman Fellow  
  
      Award Program:     Fellow  
  
      Sponsor(s) / Mentor(s):     Christopher A. Klebanoff, MD, and Michael F. Berger, PhD  
  
      Cancer Type:     All Cancers  
  
      Research Area:     Drug Discovery  
   
  





