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Clinical Immunology University Hospital Zurich Lab H1 (Office), Lab G 13/14 (Lab) Sternwartestr. 14 8091 Zurich Tel. +41 44 255 1003 Fax +41 44 255 1030 tobias.suter@usz.ch |
Our research aims at understanding the interaction of the immune system with the nervous system under both normal and inflammatory conditions.
Keywords: autoimmunity, anti-tumor immunity, neuroimmunology, antigen presentation, microglia, dendritic cells, cytokines, oligodendrocytes, de- and re-myelination, HIF-1a, HGF, transgenic mice, EAE, MS.
1 PI, 1 Research Associate, 1 Research Assistant, 1 PhD-Student.
The focus of our research is currently on the role of myeloid cells in the regulation of central nervous system (CNS) autoimmunity. To this end, we use experimental autoimmune encephalomyelitis (EAE) in mice as a model for multiple sclerosis (MS). We have been studying both the disease initiating role of dendritic cells (DC) and the role of potentially disease mitigating antigen presenting cells (APC). Currently, we are particularly intrigued by the functions that the CNS resident APC, the microglia, might execute both in propagation and resolution of the disease.
Based on our recent oligodendrocyte work,
we start in 2011 a new project funded by the SNF, in which we study the role of HIF-1a and HGF
in the repair response during CNS autoimmunity.
In vivo immunology using gene-targeted and transgenic mice, neuroinflammation and neurodegeneration models, cellular in vitro assays, protein biochemistry, molecular biology.
Moransard M, Dann A,
Staszewski O, Fontana
A, Prinz M and Suter T. NG2 expressed by
macrophages and oligodendrocyte precursor cells is dispensable in Experimental
Autoimmune Encephalomyelitis. Brain. 2011 May;134(Pt 5):1315-30. doi: 10.1093/brain/awr070.
Swiss National Research Foundation, Swiss MS-Society, NCCR Neural Plasticity and Repair, Hartmann-Müller Stiftung
http://www.klimm.usz.ch/LehreUndForschung/Seiten/Forschungsschwerpunkt.aspx
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