PHILADELPHIA -- (Dec. 14, 2017) -- A new study from The Wistar Institute revealed the mechanism implicated in the defective function of tumor-associated dendritic cells (DCs), a specialized type of immune cells that expose the antigens on their surface to activate the T cells. The new findings explain why DCs are not effective in executing a specialized process that is required for inducing antitumor immune responses and effective cancer immunotherapy. The work was published online in Nature Communications.
"Dendritic cells are essential for prompting the immune response against malignant cells and for driving the clinical success of cancer immunotherapy, but their function is often defective in cancer patients," said Dmitry I. Gabrilovich, M.D., Ph.D., Christopher M. Davis Professor and program leader of the Immunology, Microenvironment & Metastasis Program at Wistar. "Our research sheds light on the mechanism of this impairment, pointing us in the direction of new strategies for improving the response to immunotherapy."
DCs are specialized immune cells that can ingest foreign antigens, degrade them and present the fragments on their surface to activate T cell-mediated immunity. Antigens are exposed on the surface of DCs in a protein complex along with major histocompatibility complex (MHC) proteins that mediate the recognition and activation of the appropriate T cell subtype. Different classes of MHC molecules exist and are involved in immunity against pathogens and tumor cells as well as the formation of immune tolerance to self-antigens.
DCs are fundamental players in antitumor immunity through a process known as antigen cross-presentation, in which they process tumor-derived antigens into the MHC class I pathway for presentation to T cells that have the ability to kill cancer cells. This DC function is also required for the success of cancer vaccines and immunotherapy, but it is well established that tumor-associated DCs are defective in their ability to perform antigen cross-presentation. DCs from cancer patients and tumor-bearing animal models also accumulate higher amounts of lipids compared with DCs from healthy individuals, a process that has been implicated in defective cross-presentation by DCs. The mechanism underlying this association was unknown.
In collaboration with the group of Valerian Kagan, Ph.D., D.Sc., at the University of Pittsburgh, Gabrilovich and colleagues analyzed in great detail the events that take place in the DCs from tumor-bearing mice models and found that impaired cross-presentation, which occurred in the presence of tumor-derived factors, was associated with defective trafficking of the antigen-MHC complex to the cell surface. Importantly, they also observed that tumor-associated DCs accumulate chemically altered lipids that are the product of oxidative modification. Compared to unaltered lipids, these modified lipids had different ability to interact with target proteins, thus modifying their function.
Computational analysis as well as direct experiments identified some of the target proteins that strongly interact with the modified lipids, showing that these proteins are involved in the transport of the antigen-MHC complex to the cell surface. Interfering with the function of their targets, these interactions ultimately impair cross-presentation.
"Our findings present new potential targets for therapeutic regulation of cross-presentation," said Filippo Veglia, Ph.D., first author of the study and staff scientist in the Gabrilovich Lab. "For example, we investigated the effect of the antioxidant vitamin E and found that it abrogated the tumor-induced defects in cross-presentation by DCs."