نتایج جستجو برای: experimental allergic encephalomyelitis eae

تعداد نتایج: 752731  

Journal: :Proceedings of the Royal Society of Medicine 1961

Journal: :modares journal of medical sciences: pathobiology 2012
forouzan yousefi masoumeh ebtekar masoud soleimani seyed mahmoud hashemi

objective: this study investigated the effects of adipose-derived mesenchymal stem cells (mscs) and conditioned medium injection on cell infiltration in the brains of an experimental c57bl/6 mice model of autoimmune encephalomyelitis (eae). methods: eae was induced with myelin oligodendrocyte glycoprotein (35-55 peptides) in 20 mice. mscs were obtained from the adipose tissue of c57bl/6 mice a...

Journal: :Physiological research 2004
Steven M LeVine Anuradha Chakrabarty

Multiple sclerosis (MS) and its animal model, experimental allergic encephalomyelitis (EAE), are autoimmune disorders resulting in demyelination in the central nervous system (CNS). Pathologically, the blood-brain barrier becomes damaged, macrophages and T cells enter into the CNS, oligodendrocytes and myelin are destroyed, astrocytes and microglia undergo gliosis, and axons become transected. ...

Journal: :Journal of immunology 1999
N Davoust S Nataf R Reiman M V Holers I L Campbell S R Barnum

Although generally thought of as a T cell-driven autoimmune disease, recent studies in experimental allergic encephalomyelitis (EAE), the animal model of multiple sclerosis, suggest a significant role for innate immune mechanisms. To address the possibility that the complement system plays a central role in these diseases, we developed a transgenic mouse with astrocyte-targeted production of a ...

Journal: :Folia neuropathologica 2003
Barbara Kwiatkowska-Patzer Bozena Baranowska Michał Walski Andrzej W Lipkowski

A specific protein (antigen) given orally is a known method of introducing tolerance of immunological response to this antigen. This method has recently been reviewed by some authors as a possible tool in the treatment of autoaggressive diseases, such as multiple sclerosis. The experimental allergic encephalomyelitis (EAE) respected animal model for MS was used for the study. The aim of the stu...

Journal: :Journal of immunology 2003
Michaela Robbie-Ryan Melinda B Tanzola Virginia H Secor Melissa A Brown

Mast cell-deficient mice (W/W(v)) exhibit significantly reduced severity of experimental allergic encephalomyelitis (EAE), a murine model of multiple sclerosis. In this study, the contribution of FcR-mediated mast cell activation to disease was examined. W/W(v) mice were reconstituted i.v. with bone marrow-derived mast cells (BMMCs) from wild-type mice or those lacking functional FcRs. Eight we...

Sajad Sahab Negah, Sanaz Sheykhian,

Multiple sclerosis (MS) and its animal model, experimental autoimmune encephalomyelitis (EAE), are chronic inflammatory demyelinating disorders of central nervous system (CNS). While the cause is unclear, the fundamental mechanism is thought to be destruction of myelin sheaths of neurons through immune system. One of the approaches being proposed in EAE therapy is neural stem cells (NSCs) trans...

Journal: :The Journal of Experimental Medicine 1996
B M Segal E M Shevach

Inbred mice exhibit a spectrum of susceptibility to induction of experimental allergic encephalomyelitis (EAE). We have compared the immune responses of the susceptible SJL (H-2s) and resistant B10.S (H-2s) strains to determine factors other than the MHC background which control resistance/susceptibility to EAE. The resistance of the B10.S strain was found to be secondary to an antigen-specific...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Rosetta Pedotti Jason J DeVoss Sawsan Youssef Dennis Mitchell Jochen Wedemeyer Rami Madanat Hideki Garren Paulo Fontoura Mindy Tsai Stephen J Galli Raymond A Sobel Lawrence Steinman

Analysis of mRNA from multiple sclerosis lesions revealed increased amounts of transcripts for several genes encoding molecules traditionally associated with allergic responses, including prostaglandin D synthase, histamine receptor type 1 (H1R), platelet activating factor receptor, Ig Fc epsilon receptor 1 (Fc epsilon RI), and tryptase. We now demonstrate that, in the animal model of multiple ...

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