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Reprogramming Pancreatic Cancer

Findings published  in the current edition of the journal Science Translational Medicine suggest that a type of white blood cell called tumor associated macrophages that have been deceived by pancreatic cancer cells into not attacking them can be “reprogrammed” by a specially designed molecule that activates a protein found on their surfaces. 

Researchers hope that this immune system boosting molecule — ADH-503 —eventually can be used to make checkpoint inhibitor immunotherapies available to pancreatic cancer patients. Pancreatic cancer is the third deadliest cancer in the United States, but has been shown to not respond to most current immunotherapies, which have revolutionized the treatment of some other cancers. 

The paper “Agonism of CD11b reprograms innate immunity to sensitize pancreatic cancer to immunotherapies” was a collaboration between Washington University School of Medicine (WSU) in St. Louis and Rush University Medical Center in Chicago. Co-senior authors are Vineet Gupta, PhD, vice chair for research and innovation in Rush’s Department of Internal Medicine, and David DeNardo, PhD, an associate professor of medicine and of pathology and immunology at Washington University. 

The authors describe how the novel ADH-503 compound interferes with the migration and polarization of myeloid cells — a type of immune system cell that circulates through the body, identifying and attacks pathogens like cancer. A particular focus of the study was a type of myeloid cell called macrophages (Greek for “big eaters”) that are present in the tumors, since cancer cells are especially adept at disrupting the processes by which macrophages are able to control tumor growth.  

In myeloid cells, including macrophages, a receptor protein called CD11b plays a central role in recruiting them to tumors and in detecting threats and signaling whether the immune system should respond. In pancreatic cancer tumors, though, the number of macrophages that help tumors grow far outnumber those that suppress them. 

ADH-503 binds with and activates the CD11b receptor proteins on the myeloid cell surface. When the researchers orally administered the ADH-503 compound to mice with pancreatic cancer, the number of myeloid cells in and near the tumors dropped. The remaining myeloid cells were shown to be ones that promoted, rather than suppressed, immune responses. This environment resulted in greater numbers of cancer-killing T cells within the tumor, significantly slower tumor growth and longer survival.

“We believe these data demonstrate that targeting the CD11b receptor with a novel molecule can decrease TAM density and reprogram myeloid cell responses to reduce tumor growth. It also overcomes resistance to T-Cell mediated therapies.” Gupta said.   

The researchers then investigated whether creating this same environment could make pancreatic tumors susceptible to standard immunotherapy. First, they treated a control group of mice with a checkpoint inhibitor (PD-1 inhibitor) immunotherapy used to treat other kinds of cancer. There was no measurable effect. But when the therapy was combined with the ADH-503 compound, the tumors shrank and the mice survived significantly longer.

While pancreatic cancer is the third leading cause of cancer-related death in the United States, only 89 of more than 2,600 (or about 3%) 2,600 cancer immunotherapies clinical trials target pancreatic cancer

“Pancreatic cancer is a highly lethal disease, and we are in desperate need of new therapeutic approaches,” said DeNardo. “In animal studies, this small molecule led to very marked improvements and was even curative in some cases. We are hopeful that this approach could help pancreatic cancer patients.”

Phase 1 clinical trials are planned to start in the fall of 2019. The trial will assess the safety of the combined ADH-503 compound and checkpoint inhibitor immunotherapy in a small number of patients. If they treatment is found to be safe, additional studies will assess the treatment’s effectiveness.

Media Contact

Charlie Jolie
Media Relations
312-942-7817
charles_l_jolie@rush.edu

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