Christian Hinrichs, MD

Funded by the Stuart Scott Memorial Cancer Research Fund

Cancers caused by human papillomavirus (HPV), like cervical and throat cancers, are hard to treat once they spread. Our team developed a new approach called TCR-T therapy to fight HPV cancers. We take a patient’s own immune cells, called T cells, and modify the T cells in a lab so they can recognize cancer cells. After growing the cells for several weeks, we put them back into the patient. Think of it as programming T cells with a lock-and-key that fits only HPV cancer cells, allowing them to find and destroy tumors. In a clinical trial, two patients with advanced cancer saw their tumors disappear after a single treatment, and they have remained cancer-free for over a year. While successful, TCR-T therapy is slow and expensive because it must be custom-made for each patient. Some patients with fast-growing tumors simply cannot wait, and some hospitals cannot afford to offer the treatment. To solve this, we are developing a simpler treatment called a T cell engager. This protein works like double-sided tape: one side attaches to the cancer cell and the other to a T cell. By pulling the cells together, the immune system can attack the cancer. Because these proteins can be mass-produced and stored, treatment could become faster, cheaper, and more widely available. Our goal is to advance T cell engagers through lab testing and into clinical trials so more people with HPV cancers achieve lasting remission.

Location: Rutgers Cancer Institute - New Brunswick
Proposal: Off-the-shelf HPV16 TCR engagers for adult HPV-driven cancers
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