Multiple sclerosis (MS) remains the major disabling neurological illness of young adults. The consensus that MS is a T cell mediated, organ specific autoimmune disease has led to the clinical use of various immunomodulatory therapies, systemic IFN beta being the best characterized and most utilized at present. Unfortunately, while IFN beta clearly has the potential to modify the clinical course of MS, the effect is partial and not curative. Furthermore, the relevant mechanism(s) of action of IFN beta in MS remain obscure, hindering both the search for more effective therapies as well as a better understanding of the immunopathogenesis. IL-12, a cytokine central to the generation of cell mediated immune responses, is critical to the pathogenesis of experimental autoimmune encephalomyelitis, the primary experimental surrogate for MS. Further there is compelling evidence relating IL-12 production to disease activity and progression in MS itself. These investigators have found that IFN beta potently suppresses the production of IL-12 by human monocyte/macrophages. The central hypothesis underlying these studies is that a principal mechanism of action of therapeutic IFN beta in MS is the suppression of IL-12 production. The ultimate goal of this research is to use knowledge of the molecular mechanisms underlying IFN beta mediated alterations in IL-12 responses to devise novel therapeutic strategies for MS. The studies in this application aim to further characterize the effects of therapeutic IFN beta on in vivo and ex vivo IL-12 production and to characterize, in vitro, the molecular mechanisms responsible for IFN beta-mediated suppression of IL-12 production.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS039435-01A1
Application #
6199139
Study Section
Immunological Sciences Study Section (IMS)
Program Officer
Kerza-Kwiatecki, a P
Project Start
2000-07-01
Project End
2000-08-31
Budget Start
2000-07-01
Budget End
2000-08-31
Support Year
1
Fiscal Year
2000
Total Cost
$73,559
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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