Interferon beta (IFN-beta), also known as fibroblast IFN, is a secreted, approximately 22 kDa member of the type I interferon family of molecules [1]. Mature human IFN-beta shares 47% and 46% amino acid sequence identity with the mouse and rat proteins, respectively. Fibroblasts are the major producers of IFN-beta, but it can also be produced by dendritic cells, macrophages, and endothelial cells in response to pathogen exposure [2]. It is trans -criptionally regulated by TRAF3, IRF3, IRF7, and NF-kappa B [3]. Following secretion, IFN-beta signals through the heterodimeric IFN-alpha / beta Receptor and activates the JAK/STAT signaling pathway [4-7]. IFN-beta -deficient mice show increased susceptibility to experimental autoimmune encephalomyelitis (EAE), a disease model of human multiple sclerosis (MS) [8]. Furthermore, IFN-beta has been shown to suppress the Th17 cell response in both MS and EAE and has commonly been used as a treatment for MS [9-13].
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