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Cancer immunotherapy—an approach that removes the barriers that protect cancer cells from a patient’s immune system—has revolutionized the treatment of many cancer types. About 40 percent of melanoma patients, for example, respond to immunotherapy, enabling the immune system’s T cells to attack cancer cells and take control of the disease.
In a study published in the February 6, 2019 issue of Nature, a University of Chicago-based team working in collaboration with scientists at Tsinghua University and the Chinese Academy of Sciences, demonstrates, in mice, that they can boost the tumor control rate from around 40 percent up to nearly 100 percent by opening up a parallel pathway.
This study relies on manipulating these cells, which are a crucial component of the immune system. The primary function of dendritic cells is to process antigens and present them to T cells. They act as messengers, connecting the innate and the adaptive immune systems.
But a protein known as YTHDF1 influences antigen processing by dendritic cells. This protein was discovered and characterized in 2015 by Chuan He, PhD, the John T. Wilson Distinguished Service Professor in chemistry, biochemistry and molecular biology, and the Institute for Biophysical Dynamics at the University of Chicago. YTHDF1 controls the level of proteases that destroy potential tumor antigens. This limits their presentation to T cells.
These limits were a problem, He said. But when he and his colleagues eliminated YTHDF1, the dendritic cells increased their ability to engulf peptides, degrade them and present them to T cells. This opened up a new and potentially effective approach to treatment of cancer in patients who do not respond well to checkpoint inhibitors.
“Once we combined YTHDF1 knock-out with the checkpoint inhibitor anti PD-L1, we got almost complete tumor control in a mouse model,” He said. Instead of a 40 percent response, nearly 100 percent of treated mice with melanoma responded to anti-PD-L1.
This study opens a lot of doors. It provides a whole new set of targets to the immune system, ranging from new sets of antigens to potential anti-cancer vaccines.
The researchers confirmed that dendritic cells from mice that lacked YTHDF1 were more effective at antigen-presentation than dendritic cells from normal, wild-type mice. “Our data show that loss of YTHDF1 in dendritic cells attenuates antigen degradation and leads to improved cross-presentation and better cross-priming of CD8 + T cells,” according to co- corresponding author Dali Han, PhD, now at the Beijing Institute of Genomics.
Together with gastroenterologist Marc Bissonnette, MD, associate professor of medicine at the University of Chicago, He’s team performed an additional test using biopsies from human patients with colon cancer, a disease that is much less responsive to immunotherapy than melanoma. They found that tissue from patients with high levels of YTHDF1 had limited T cell infiltration, but patients with low levels of YTHDF1 had more T cell infiltrates. “This suggests that humans correlate nicely with our mouse data,” He added.
“An important question in cancer treatment is ‘how could we get better antigen presentation?’” according to co-author Ralph Weichselbaum, MD, the Daniel K. Ludwig Distinguished Service Professor and chairman of radiation oncology at the University of Chicago. “This study opens a lot of doors,” he said. “It provides a whole new set of targets to the immune system, ranging from new sets of antigens to potential anti-cancer vaccines. This is the type of cross-divisional, interdisciplinary collaboration that could lead to unexpected discoveries.”
This supports the notion that reduced YTHDF1 often coincides with the T cell inflamed tumor microenvironment, which is crucial for successful immunotherapy, the authors note. YTHDF1 could be a therapeutic target for immunotherapy in combination with emerging checkpoint inhibitors or dendritic cell vaccines.
“It will be really interesting to test how the human system works with potential dendritic cell vaccines or small molecule inhibitors that can suppress the activity of YTHDF1 in human cancer patients,” according to corresponding author Meng Michelle Xu, PhD, a former member of the He and Weichselbaum laboratories.
“We have not yet seen any measurable toxicity, as far as we can tell, related to knocking down YTHDF1 in mice,” He added. “At this point, this appears to be a very benign system. We hope to begin early testing in patients within one year.”
The National Key Research and Development Program of China, the Strategic Priority Research Program of the Chinese Academy of Sciences, the National Institutes of Health, The Ludwig Center at the University of Chicago, the National Natural Science Foundation of China, the National Science Fund for Excellent Young Scholars, the Science Foundation for Distinguished Young Scholars of China, and the National Science Foundation. Additional authors include Jun Liu, Chuanyuan Chen, Lihui Dong, Yi Liu, Renbao Chang, Xiaona Huang, Yuanyuan Liu, Jianying Wang, Bin Shen, Urszula Dougherty and Marc Bissonnette.
Chuan He, PhD, is the John T. Wilson Distinguished Service Professor of Chemistry at UChicago. His research spans a broad range of chemical biology, nucleic acid chemistry and biology, epigenetics, and bioinorganic chemistry.Learn more about Dr. He
Ralph R. Weichselbaum, MD, specializes in the potentially curative treatment of oligometastasis with radiation therapy. He serves as chair of the Department of Radiation and Cellular Oncology.View Dr. Weichselbaum's physician profile