Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3065915 | Journal of Neuroimmunology | 2006 | 13 Pages |
Abstract
Gene knock-out and knock-in mice are becoming increasingly indispensable for mechanism-oriented studies of EAE. Most gene-modified mice are on the C57BL/6 background, for which presently there are only two EAE models available, the MOG peptide 35–55 and the PLP 178–191 peptide induced disease. However, because MS is not a single pathogenic entity, different EAE models are required to reproduce and study its various features. Here we are introducing MBP-PLP fusion protein (MP4)-induced EAE for C57BL/6 mice. B cell- and CD8+ T cell-dependence, as well as multi-determinant recognition are among the unique features of this demyelinating EAE.
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Authors
Stefanie Kuerten, Felix S. Lichtenegger, Susan Faas, Doychin N. Angelov, Magdalena Tary-Lehmann, Paul V. Lehmann,