Smart Cancer Therapies: Teaching the Body’s Own T-cells to Attack Tumors

Kris Saha
Kris Saha

University of Wisconsin-Madison engineers are manufacturing specific and highly personalized cancer treatments that take advantage of a patient’s own cells to attack tumors.

These so-called Chimeric Antigen Receptor (CAR) T-Cell therapies have already shown tremendous potential in treating blood-based cancers, such as leukemia. Now, with support from a two-year grant from the National Science Foundation, they are investigating ways to make these cutting-edge therapies more versatile and practical.

“It’s really exciting to work in the CAR T-Cell research space,” says Krishanu Saha, an assistant professor of biomedical engineering at UW-Madison. “It’s research that is close to the clinic.”

Working with colleague David Beebe, the John D. MacArthur Professor & Claude Bernard Professor in biomedical engineering, and Christian Capitini, an assistant professor of pediatrics at UW-Madison, Saha aims to develop improved methods for making CAR T-Cells, and to test their efficacy against a broad array of tumor types.

“This is a really good use of the engineering talent on campus in partnership with the excellent clinicians here at UW-Madison,” says Saha.

Unlike traditional cancer treatments like radiation and chemotherapy, which indiscriminately poison all rapidly-dividing cells inside of a patient—and in the process cause a whole host of devastating of side-effects—CAR T-cell treatments use genetic engineering to improve upon the body’s own defense mechanisms and specifically eliminate cancer.

Florescent imaging
The researchers use fluorescent imaging to monitor engineered T-cell cultures. After identifying promising strategies using cell lines, they plan to develop animal models to test personalized cancer therapies.

T-cells are the body’s targeted killers: They seek out and destroy potential threats such as invading bacteria or virus-infected tissue. T-cells have features on their surfaces called receptors that recognize their targets. Recently, scientists figured out a way to isolate T-cells from patients and add special artificial receptors to those cells in order to reeducate the microscopic assassins. Those engineered cells, now bearing a so-called “Chimeric Antigen Receptor” (CAR) on their surfaces, attack cancer with startling efficiency when reintroduced to patients’ bodies.

Early clinical trials involving CAR T-cells have shown tremendous promise; in one test the therapy eliminated all traces of leukemia from 90 percent of patients.

However, despite these early successes, some aspects of CAR T-cell treatments remain challenging. Because T-cells don’t grow very well outside of a patient’s body, biomedical engineers have a limited window of time to work with the samples and make the necessary modifications. Additionally, most strategies to add the chimeric antigen to the cells rely on viruses, which sometimes causes additional, unexpected changes.

“We’re trying to attack the problem of manufacturing T-cells in a process that is easy to control, understand, and scale up in a clinical setting,” says Saha. “Our approach uses perhaps a more controlled way of inserting the CAR.”

“To me this is the tip of the iceberg for how synthetic biology will penetrate in the human body.”
-Kris Saha

Their approach relies on CRISPR, the genetic engineering technique that allows researchers to precisely rewrite genomes with relative ease. Saha is rapidly becoming a leader in the technology, with several ongoing projects to uncover deeper understanding of how CRISPR makes changes inside human cells.

In addition to improving the production of CAR T-cells, the researchers plan to make the revolutionary therapy applicable to a broader array of cancers. Currently, CAR T-cells have been shown to treat blood-based cancers highly effectively, but clinicians have seen little success applying the therapies to solid tumors.

During the next two years, Saha will first identify promising CAR T-cell therapies for solid cancer cell lines growing in glass dishes, then develop animal models—a first step in developing any new treatment for human patients. Based on early successes, however, the potential for these types of treatments seems almost limitless.

“To me this is the tip of the iceberg for how synthetic biology will penetrate in the human body,” says Saha.

The research is supported by the National Science Foundation’s Early-concept Grants for Exploratory Research (EAGER) program, which prioritizes potentially transformative, research, radically different approaches, and novel interdisciplinary perspectives.

Sam Million-Weaver

This article originally appeared on the College of Engineering website at