Cells belonging to the body's own immune system can help fight tumors. For several years now, this has allowed oncologists to use medications known as checkpoint inhibitors to encourage T cells to eliminate tumor cells. Last year the two scientists who discovered this therapeutic approach were awarded the Nobel Prize for Medicine.
While doctors are enjoying some initial successes with this method, especially with regard to melanomas and several other types of cancer, immunologists and cancer researchers are working to develop the approach further. What they have in mind is a vaccine that would cause cancer-repelling T cells to multiply in the body, thereby strengthening the body's immune defenses. The big question is which molecules are suitable for a vaccine? Researchers working in the team of Manfred Kopf, Professor of Molecular Biomedicine, have now developed a method for identifying such molecules.
The search for a rapport between immune cells and tumor cells
Since on the one hand tumors differ greatly from patient to patient, and on the other no two people (except identical twins) have the same immune system, future immunization against cancer is a complex example of personalized medicine. The goal is to develop an individual vaccine for each patient.
Potential vaccines include pieces of proteins, known as peptides, that are found only in tumors due to a mutation. Because T cells are specific and always recognize only one particular peptide, just as a key fits only one lock, a further prerequisite for a vaccine of this kind is that the patient has T cells capable of recognizing these cancer peptides in the first place. So before doctors can immunize a cancer patient, laboratory tests must be conducted to search for corresponding pairs of T cells and peptides. A peptide that is recognized by a T cell can be used for personalized immunization. The vaccine should then activate the T cells in the body that recognize only that peptide (and thus tumor cells). These T cells should ultimately wipe out the tumor.
The ETH researchers' method makes it possible for a laboratory to determine which T cells recognize which peptide. Up to now this has been incredibly difficult. The scientists used tumors in mice to show that their approach works. Next, they want to demonstrate the effectiveness of their approach in dealing with tumors in humans.
Every patient gets their own set of reporter cells
At the heart of this new method lies a collection of several million reporter cells, each one of which presents on its cell surface one of many peptides found in a tumor. The reporter cells are designed to turn green as soon as a T cell interacts with it due to recognition of the presented peptide. This enables the scientists to identify those tumor peptides that the T cells of a cancer patient recognizes. This involves mixing the collection of reporter cells with T cells taken from the patient's tumor, isolating the reporter cells that turn green and identifying the peptide they carry.
Since each person (and each vertebrate generally) has a unique immune system, and since each tumor carries a unique pattern of mutations, the scientists must produce a different set of reporter cells for each patient. "One option is to determine the tumor's genetic sequence and compare it with the gene sequence of the patient's healthy cells," Kopf says. This lets the researchers determine the extent to which the tumor differs from healthy tissue and then transfer the genetic information with precisely these tumor-specific differences into the reporter cells.
As Kopf explains, "Other scientists are using computer predictions to try and find out which cancer peptides are suited to this type of immunization. But this approach is only as good as the algorithms used - and at the moment, they aren't very reliable. By contrast, we have developed an experimental test that assures us that the T cells recognize patient tumor peptides."
Initial tests involving a breast cancer model in mice showed Kopf and his colleagues that their method works. In immunized mice, the immune system did indeed attack the tumor; in the non-immunized mice that the scientists used as a control, this did not happen.
The scientists already patented this method five years ago. In 2015, their promising discovery won them ETH Zurich's Spark Award. Their work was recently published in the specialist journal Nature Immunology.
To develop commercial applications for the technique, the scientists founded an ETH spin-off called Tepthera. This start-up plans to demonstrate the effectiveness of their approach also using tumors in humans.
Just as interesting for autoimmune diseases
"Essentially, our technique and personalized immunization hold out promise for the treatment of all cancers - especially in combination with checkpoint inhibitors," Kopf says, adding that the technology could also be used in the research and treatment of autoimmune diseases such as multiple sclerosis or type 1 diabetes.
Unlike healthy people's immune system, the immune system in people who suffer from autoimmune diseases attacks not only foreign or mutated cells, but also the autoimmune patient's own body cells. In the case of many of these conditions, it is not yet known against which native molecules the autoimmune response is directed. This is something that can now be researched using the new method. In contrast to cancer, where the idea is to use immunization to activate the killer cells, for autoimmune diseases the aim is to develop a vaccine that tempers the immune system.
This article has been republished from materials provided by ETH Zurich. Note: material may have been edited for length and content. For further information, please contact the cited source.