| Literature DB >> 18565596 |
Jan Hilpert1, Johanna M Beekman, Susanne Schwenke, Kristin Kowal, David Bauer, Johannes Lampe, Rupert Sandbrink, Jürgen F Heubach, Steffen Stürzebecher, Joachim Reischl.
Abstract
Treatment with interferon beta-1b (IFNB-1b) is clinically effective in multiple sclerosis patients. However, the mechanism of action is only partially understood, and validated biological response markers are lacking. We assessed IFNB-1b-induced transcriptional changes by microarray technology. Healthy male volunteers received 250 mug IFNB-1b or placebo in a double-blind, randomized controlled trial (n=5 per group). Most transcripts demonstrated peak levels after 6-12 h and returned to baseline after 48 h. We identified 227 differentially regulated genes including novel and previously described markers. This panel may become a valuable tool for development of new IFNB-1b formulations and assessment of clinical drug effects.Entities:
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Year: 2008 PMID: 18565596 DOI: 10.1016/j.jneuroim.2008.04.036
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478