The role of interferon (IFN)-gamma in multiple sclerosis (MS) and its animal model, experimental autoimmune encephalomyelitis (EAE), has remained as an enigmatic paradox for more than 30 years. Several studies attribute this cytokine a prominent proinflammatory and pathogenic function in these pathologies. However, accumulating evidence shows that IFN-gamma also plays a protective role inducing regulatory cell activity and modulating the effector T cell response. Several innate and adaptive immune cells also develop opposite functions strongly associated with the production of IFN-gamma in EAE. Even the suppressive activity of different types of regulatory cells is dependent on IFN-gamma Interestingly, recent data supports a stage-specific participation of IFN-gamma in EAE providing a plausible explanation for previous conflicting results. In this review, we will summarize and discuss such literature, emphasizing the protective role of IFN-gamma on immune cells. These findings are fundamental to understand the complex role of IFN-gamma in the pathogenesis of these diseases and can provide basis for potential stage-specific therapy for MS targeting IFN-gamma-signaling or IFN-gamma producing immune cells. Keywords. Author Keywords:interferon-gamma; experimental autoimmune encephalomyelitis; multiple sclerosis; innate immunity; adaptive immunity; neuroinflammation . KeyWords Plus:EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; CENTRAL-NERVOUS-SYSTEM; NATURAL-KILLER-CELLS; DELTA T-CELLS; MONOCLONAL-ANTIBODY TREATMENT; INVARIANT NKT CELLS; IFN-GAMMA; REGULATORY ROLE; NITRIC-OXIDE; TNF-ALPHA