Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis

被引:27
|
作者
Kebir, Hania [1 ,2 ]
Carmant, Lionel [3 ,4 ,5 ]
Fontaine, Francois [3 ,4 ]
Beland, Kathie [3 ]
Bosoi, Ciprian M. [3 ]
Sanon, Nathalie T. [3 ]
Alvarez, Jorge I. [6 ]
Desgent, Sebastien [3 ]
Pittet, Camille L. [2 ]
Hebert, David [3 ]
Langlois, Marie-Josee [3 ]
Rebillard, Rose-Marie [4 ]
Nguyen, Dang K. [2 ,5 ]
Cieuta-Walti, Cecile [7 ]
Holmes, Gregory L. [8 ]
Goodkin, Howard P. [9 ]
Mytinger, John R. [9 ,11 ]
Connolly, Mary B. [10 ]
Prat, Alexandre [2 ,5 ]
Haddad, Elie [1 ,3 ,4 ]
机构
[1] Univ Montreal, Dept Microbiol Infect Dis & Immunol, Fac Med, Montreal, PQ, Canada
[2] Univ Montreal, CRCHUM, Fac Med, Montreal, PQ, Canada
[3] CHU St Justine, Ctr Rech, 3175 Chemin Cote St Catherine, Montreal, PQ H3T 1C5, Canada
[4] Univ Montreal, Fac Med, Dept Pediat, Montreal, PQ, Canada
[5] Univ Montreal, Fac Med, Dept Neurosci, Montreal, PQ, Canada
[6] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
[7] Univ Sherbrooke, Dept Pediat, CHU Sherbrooke, Sherbrooke, PQ, Canada
[8] Univ Vermont, Larner Coll Med, Dept Neurol Sci, Burlington, VT USA
[9] Univ Virginia, Dept Pediat, Fontaine Res Pk, Charlottesville, VA USA
[10] Univ British Columbia, BC Childrens Hosp, Div Neurol, Dept Pediat, Vancouver, BC, Canada
[11] Ohio State Univ, Dept Pediat, Div Pediat Neurol, Nationwide Childrens Hosp, Columbus, OH 43210 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2018年 / 128卷 / 05期
基金
加拿大健康研究院;
关键词
GLUTAMATE-RECEPTOR; T-CELLS; ANTIBODIES; EPILEPSY; GLUR3; AUTOANTIBODIES; THERAPY; SYSTEM; BRAIN; CYTOMEGALOVIRUS;
D O I
10.1172/JCI97098
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rasmussen's encephalitis (RE) is a chronic inflammatory brain disorder that causes frequent seizures and unilateral hemispheric atrophy with progressive neurological deficits. Hemispherectomy remains the only treatment that leads to seizure freedom for this refractory epileptic syndrome. The absence of an animal model of disease has been a major obstacle hampering the development of effective therapies. Here, we describe an experimental mouse model that shares several clinical and pathological features with the human disease. Immunodeficient mice injected with peripheral blood mononuclear cells from RE patients and monitored by video electroencephalography developed severe seizures of cortical origin and showed intense astrogliosis and accumulation of human IFN-gamma- and granzyme B-expressing T lymphocytes in the brain compared with mice injected with immune cells from control subjects. We also provide evidence for the efficacy of alpha 4 integrin blockade, an approved therapy for the treatment of multiple sclerosis and Crohn's disease, in reducing inflammatory markers associated with RE in the CNS. This model holds promise as a valuable tool for understanding the pathology of RE and for developing patient-tailored experimental therapeutics.
引用
收藏
页码:2000 / 2009
页数:10
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