MOGAD is a disease in which the immune system mistakenly produces antibodies that target the MOG protein. This presumably damages the protective myelin layer around nerve cells, leading to inflammation in the central nervous system. However, until now, it has been difficult to study the mechanisms that cause the disease because the structure of the anti-MOG antibodies was unknown. In regard to therapy, it is important to distinguish the autoimmune disease MOGAD, that occurs in episodes and can affect the brain, optic nerve and spinal cord, from multiple sclerosis (MS).
White blood cells contain instructions for building MOG antibodies
The international research team led by Prof. Anne-Katrin Pröbstel from the UKB and the Universities of Basel and Bonn succeeded in identifying MOG-reactive B cells, the antibody factories of the immune system, in patient blood. These contained the genetic instructions for the anti-MOG antibodies. "Based on this alone, we were able to determine that MOG reactivity is present in different B cell subtypes," says Dr. Nora Wetzel, and Dr. Laila Kulsvehagen adds: "For example, there are B cells that are specific to MOG from the outset, while other B cells only develop this reactivity as they mature." The two co-first authors of the study belong to Prof. Pröbstel's research group.
The genetic code also allowed the researchers to produce the antibodies in the laboratory and test their functions. This revealed that the antibodies use various mechanisms to eliminate MOG-producing cells. "Interestingly, not all MOG antibodies were equally effective in using these different mechanisms. While this was partly due to the binding capacity of the antibodies, we suspect that the structural interaction between the MOG antigen and the antibody is relevant, especially for the activation of the immune cascade," says Prof. Pröbstel, director of the Center for Neurology at the University Hospital Bonn (UKB), member of the ImmunoSensation2 Cluster of Excellence at the University of Bonn and research group leader at the German Center for Neurodegenerative Diseases (DZNE).
This study confirms previous work involving patient sera and brain autopsies, thus reinforcing the hypothesis that anti-MOG antibodies contribute to the development of the disease, known in technical terms as pathogenesis. Prof. Pröbstel emphasizes: "The new understanding of the origin of MOG-reactive B cells and antibody functions is important for developing tailored therapies."