Targeting CD73 in the tumor microenvironment with MEDI9447

Carl Hay(Altimmune (United States)), Erin Sult(Altimmune (United States)), Qihui Huang(Altimmune (United States)), Kathy Mulgrew(Altimmune (United States)), Stacy Fuhrmann(Altimmune (United States)), Kelly McGlinchey(Altimmune (United States)), Scott A. Hammond(Altimmune (United States)), Raymond Rothstein(Altimmune (United States)), Jonathan Rios‐Doria(Altimmune (United States)), Edmund Poon(Aimmune Therapeutics (United Kingdom)), Nick Holoweckyj(Altimmune (United States)), Nicholas M. Durham(Altimmune (United States)), Ching Ching Leow(AstraZeneca (Netherlands)), Gundo Diedrich(MacroGenics (United States)), Melissa Damschroder(Altimmune (United States)), Ronald Herbst(Altimmune (United States)), Robert E. Hollingsworth(Altimmune (United States)), Kris F. Sachsenmeier(Altimmune (United States))
OncoImmunology
July 11, 2016
Cited by 286Open Access
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Abstract

MEDI9447 is a human monoclonal antibody that is specific for the ectoenzyme CD73 and currently undergoing Phase I clinical trials. Here we show that MEDI9447 is a potent inhibitor of CD73 ectonucleotidase activity, with wide ranging immune regulatory consequences. MEDI9447 results in relief from adenosine monophosphate (AMP)-mediated lymphocyte suppression in vitro and inhibition of mouse syngeneic tumor growth in vivo. In contrast with other cancer immunotherapy agents such as checkpoint inhibitors or T-cell agonists, MEDI9447 drives changes in both myeloid and lymphoid infiltrating leukocyte populations within the tumor microenvironment of mouse models. Changes include significant alterations in a number of tumor micro-environmental subpopulations including increases in CD8(+) effector cells and activated macrophages. Furthermore, these changes correlate directly with responder and non-responder subpopulations within animal studies using syngeneic tumors. Combination data showing additive activity between MEDI9447 and anti-PD-1 antibodies using human cells in vitro and mouse tumor models further demonstrate the potential value of relieving adenosine-mediated immunosuppression. Based on these data, a Phase I study to test the safety, tolerability, and clinical activity of MEDI9447 in cancer patients was initiated (NCT02503774).


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