Induction of pregnancy during established EAE halts progression of CNS autoimmune injury via pregnancy-specific serum factors

被引:45
作者
Gatson, NaTosha N. [1 ]
Williams, Jessica L. [1 ]
Powell, Nicole D. [1 ]
McClain, Melanie A. [1 ]
Hennon, Teresa R. [2 ]
Robbins, Paul D. [2 ]
Whitacre, Caroline C. [1 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Univ Pittsburgh, Dept Microbiol & Mol Genet, Pittsburgh, PA 15219 USA
关键词
Multiple sclerosis; Experimental autoimmune encephalomyelitis; Pregnancy; Exosomes; Autoimmunity; MULTIPLE-SCLEROSIS PATIENTS; HORMONE-THERAPY; ENCEPHALOMYELITIS; FOREBRAIN; EXOSOMES; ESTROGEN; RELAPSES; STRAINS; RISK;
D O I
10.1016/j.jneuroim.2010.09.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is a demyelinating disease of the CNS involving T cell targeting of myelin antigens. During pregnancy, women with MS experience decreased relapses followed by a post partum disease flare. Using murine experimental autoimmune encephalomyelitis, we recapitulate pregnancy findings in both relapsing and progressive models. Pregnant mice produced less TNF-alpha, IL-17 and exhibited reduced CNS pathology relative to non-pregnant controls. Microparticles, called exosomes, shed into the blood during pregnancy were isolated and found to significantly suppress T cell activation relative to those from non-pregnant controls. These results demonstrate the immunosuppressive potential of pregnancy and serum-derived pregnancy exosomes. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
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