Glatiramer acetate (GA; Copaxone) is an approved drug for the treatment of multiple sclerosis (MS). The underlying multifactorial anti-inflammatory, neuroprotective effect of GA is in the induction of reactive Tcells that release immu-nomodulatory cytokines and neurotrophic factors at the injury site. These GA-induced cytokines and growth fac-tors may have a direct effect on axon function. Building on previous findings that suggest a neuroprotective effect of GA, we assessed the therapeutic effects of GA on brain and spinal cord pathology and functional correlates using the chronic experimental autoimmune encephalomyelitis (EAE) mouse model of MS. Therapeutic regimens were uti-lized based on promising prophylactic efficacy. More spe-cifical...
Glatiramer acetate (GA) is a synthetic amino acid copolymer that is approved for treatment of relaps...
Mechanisms underlying the clinical benefits of glatiramer acetate (GA) for patients with multiple sc...
The relationship between immune responses to self-antigens and autoimmune disease is unclear. In con...
Glatiramer acetate (GA; Copaxone) is an approved drug for the treatment of multiple sclerosis (MS). ...
Glutamate-mediated excitotoxicity is supposed to induce neurodegeneration in multiple sclerosis (MS)...
Multiple sclerosis (MS) is considered to be primarily an inflammatory autoimmune disease. Over the l...
Multiple sclerosis (MS) is considered to be primarily an inflammatory autoimmune disease. Over the l...
Axonal and neuronal pathologies are a central constituent of multiple sclerosis (MS) and its animal ...
Glatiramer acetate (GA, Copaxone((R))), a standardized mixture of synthetic polypeptides, has now be...
The immunomodulador glatiramer acetate (GA) has been shown to significantly reduce the severity of s...
Background: Glatiramer acetate (GA) is a well-established treatment option for patients with clinica...
Glatiramer acetate (GA; Copaxone) is a random copolymer of glutamic acid, lysine, alanine, and tyros...
EAE is a common animal model for multiple sclerosis (MS). Immunomodulatory treatments such as glatir...
Glatiramer acetate is a synthetic, random copolymer widely used as a first-line agent for the treatm...
AbstractGlatiramer acetate (Copaxone®; GA) is a non-biological complex drug for multiple sclerosis. ...
Glatiramer acetate (GA) is a synthetic amino acid copolymer that is approved for treatment of relaps...
Mechanisms underlying the clinical benefits of glatiramer acetate (GA) for patients with multiple sc...
The relationship between immune responses to self-antigens and autoimmune disease is unclear. In con...
Glatiramer acetate (GA; Copaxone) is an approved drug for the treatment of multiple sclerosis (MS). ...
Glutamate-mediated excitotoxicity is supposed to induce neurodegeneration in multiple sclerosis (MS)...
Multiple sclerosis (MS) is considered to be primarily an inflammatory autoimmune disease. Over the l...
Multiple sclerosis (MS) is considered to be primarily an inflammatory autoimmune disease. Over the l...
Axonal and neuronal pathologies are a central constituent of multiple sclerosis (MS) and its animal ...
Glatiramer acetate (GA, Copaxone((R))), a standardized mixture of synthetic polypeptides, has now be...
The immunomodulador glatiramer acetate (GA) has been shown to significantly reduce the severity of s...
Background: Glatiramer acetate (GA) is a well-established treatment option for patients with clinica...
Glatiramer acetate (GA; Copaxone) is a random copolymer of glutamic acid, lysine, alanine, and tyros...
EAE is a common animal model for multiple sclerosis (MS). Immunomodulatory treatments such as glatir...
Glatiramer acetate is a synthetic, random copolymer widely used as a first-line agent for the treatm...
AbstractGlatiramer acetate (Copaxone®; GA) is a non-biological complex drug for multiple sclerosis. ...
Glatiramer acetate (GA) is a synthetic amino acid copolymer that is approved for treatment of relaps...
Mechanisms underlying the clinical benefits of glatiramer acetate (GA) for patients with multiple sc...
The relationship between immune responses to self-antigens and autoimmune disease is unclear. In con...