| Literature DB >> 16781782 |
Stefanie Kuerten1, Felix S Lichtenegger, Susan Faas, Doychin N Angelov, Magdalena Tary-Lehmann, Paul V Lehmann.
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.Entities:
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Year: 2006 PMID: 16781782 DOI: 10.1016/j.jneuroim.2006.03.021
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478