Possible role of the innate immunity in temporal lobe epilepsy
Article first published online: 11 DEC 2007
© 2008 International League Against Epilepsy
Volume 49, Issue 6, pages 1055–1065, June 2008
How to Cite
Van Gassen, K. L.I., De Wit, M., Koerkamp, M. J.A. G., Rensen, M. G.A., Van Rijen, P. C., Holstege, F. C.P., Lindhout, D. and De Graan, P. N.E. (2008), Possible role of the innate immunity in temporal lobe epilepsy. Epilepsia, 49: 1055–1065. doi: 10.1111/j.1528-1167.2007.01470.x
- Issue published online: 11 DEC 2007
- Article first published online: 11 DEC 2007
- Accepted November 2, 2007; Online Early publication December 12, 2007.
- Temporal lobe epilepsy;
- Immune system
Purpose: Temporal lobe epilepsy (TLE) is a multifactorial disease often involving the hippocampus. So far the etiology of the disease has remained elusive. In some pharmacoresistant TLE patients the hippocampus is surgically resected as treatment. To investigate the involvement of the immune system in human TLE, we performed large-scale gene expression profiling on this human hippocampal tissue.
Methods: Microarray analysis was performed on hippocampal specimen from TLE patients with and without hippocampal sclerosis and from autopsy controls (n = 4 per group). We used a common reference pool design to perform an unbiased three-way comparison between the two patient groups and the autopsy controls. Differentially expressed genes were statistically analyzed for significant overrepresentation of gene ontology (GO) classes.
Results: Three-way analysis identified 618 differentially expressed genes. GO analysis identified immunity and defense genes as most affected in TLE. Particularly, the chemokines CCL3 and CCL4 were highly (>10-fold) upregulated. Other highly affected gene classes include neuropeptides, chaperonins (protein protection), and the ubiquitin/proteasome system (protein degradation).
Discussion: The strong upregulation of CCL3 and CCL4 implicates these chemokines in the etiology and pathogenesis of TLE. These chemokines, which are mainly expressed by glia, may directly or indirectly affect neuronal excitability. Genes and gene clusters identified here may provide targets for developing new TLE therapies and candidates for genetic research.