Researchers at the Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch and Charité -- Universitätsmedizin Berlin, Campus Berlin-Buch, have succeeded in generating cells of the immune system to specifically target and destroy cancer cells. The research findings of Matthias Obenaus, Professor Thomas Blankenstein (MDC and Charité), Dr. Matthias Leisegang (MDC), and Professor Wolfgang Uckert (Humboldt-Universität zu Berlin and MDC), as well as Professor Dolores Schendel (Medigene AG, Planegg/Martinsried) have now been published.
The immune system of the body is trained to distinguish between "foreign" and "self" and to recognize and destroy exogenous structures. In cancer, however, the immune system appears to be quite docile in its response. While it is capable of detecting cancer cells because they often bear characteristics (antigens) on their surfaces that identify them as pathologically altered cells, usually the immune system does not mount an attack but rather tolerates them. The reason: The cancer cells are endogenous to the body, and immune cells do not recognize them as foreign, as they would pathogens. The researchers want to break this tolerance in order to develop therapies against cancer.
T cells are the linchpin in the attack of the immune system. On their surface they have anchor molecules (receptors) with which they recognize foreign structures, the antigens of bacteria or viruses, and thus can target and destroy invaders. Cancer researchers and immunologists are attempting to mobilize this property of the T cells in the fight against cancer. The objective is to develop T cells that specifically recognize and attack only cancer cells but spare other body cells.
Now Matthias Obenaus, Professor Blankenstein, Dr. Leisegang, Professor Uckert, and Professor Schendel have developed human T cell receptors (TCRs) that have no tolerance toward human cancer antigens and specifically recognize the antigen MAGE-A1, which is present on various human tumor cells. Instead of directly using human-derived TCRs, which do not mediate substantial anti-tumor effects, the scientists took a "detour" over a mouse model.
First, the researchers transferred the genetic information for human TCRs into the mice, thus creating an entire arsenal of human TCRs. When the humanized mouse T cells come into contact with human cancer cells, they perceive the tumor antigens as foreign -- like viral or bacterial antigens. Thus, the T cells can specifically target, attack, and destroy the tumor cells.
The researchers subsequently isolated the human T-cell receptors of these mice, which are specifically targeted toward the tumor antigen MAGE-A1. Then they transferred the T-cell receptors into human T cells, thereby training them to recognize the cancer cells as foreign.
Some people possess T cells which naturally recognize MAGE-A1 on tumor cells, but only in the Petri dish. In studies using an animal model, only the human TCRs derived from mice were shown to be effective against the tumor. The TCRs from human T cells ignored the tumor completely. The comparison with the tweaked human TCRs from the mouse model shows that the TCRs of patients cannot recognize the tumor antigens sufficiently; they are too weak.
"The fact that our TCRs from the mouse are better is a strong indication that the T cells of a human are tolerant toward MAGE-A1," said Matthias Obenaus and Professor Blankenstein.
Using the T-cell receptors they developed, the researchers are planning an initial clinical trial with patients with MAGE-A1 positive multiple myeloma, a malignant disease of the bone marrow.
Max Delbrueck Center for Molecular Medicine (MDC) Berlin-Buch News Release (03/19/15)
Science Daily (03/19/15)
Abstract (Nature Biotechnology; 33, 402-407 (03/16/15))
Abstract (Nature Medicine; 16, 1029-1034 (08/08/10))