作者: Yolanda S. Kap , Jon D. Laman , Bert A. ‘t Hart
DOI: 10.1007/S11481-009-9178-Y
关键词: Experimental autoimmune encephalomyelitis 、 Multiple sclerosis 、 Immunotherapy 、 Myelin oligodendrocyte glycoprotein 、 Interleukin 23 、 Marmoset 、 Neuroscience 、 Central nervous system 、 Immunology 、 Biology 、 Callithrix
摘要: The attrition rate of new drugs for central nervous system diseases including multiple sclerosis (MS) is very high. A widely recognized bottleneck in the selection promising drug candidates from development pipeline lack sufficiently predictive animal models. Here, we review how experimental autoimmune encephalomyelitis (EAE) model Neotropical primate “common marmoset” can help to bridge gap between rodent EAE models and MS. marmoset closely resembles MS clinical as well pathological presentation be used fundamental research into immunopathogenic mechanisms therapy development. We discuss recent insights arising this model, both on novel therapeutics immunopathogenesis.