The main goal of our research is to better understand the link between the immune and the central nervous systems. We are particularly focused on how CD8 T cells are activated in the central nervous system, and how we can translate this knowledge into potential therapeutic strategies for neurodegeneration. Our latest work uncovered an unexpected role of CD8 T cells in a juvenile and slowly progressive form of the neurodegenerative disease Amyotrophic Lateral Sclerosis 4 (ALS4), which is caused by a mutation in the gene SETX. We found that clonally expanded CD8 T cells of likely autoimmune origin are progressively activated in the central nervous system (CNS) and blood of patients and mice. In ALS4 mice, clonal expansion of CD8 T cells in the CNS correlates with disease progression. Starting from these original results, our lab will further explore the role of CD8 T cells in the pathogenesis of several forms of ALS, in both humans and mice. Techniques include, but are not limited to, molecular biology and cloning, T cell transduction, flow cytometry, imaging, in vitro and in vivo assays, behavioral tests, and RNA-sequencing. Collaborates on designing, conducting and reporting of research projects.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree