Antibody-mediated remyelination operates through mechanism independent of immunomodulation

被引:27
作者
Ciric, B
Van Keulen, V
Soldan, MP
Rodriguez, M
Pease, LR
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Dept Immunol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Coll Med, Dept Program Mol Neurosci, Rochester, MN 55905 USA
关键词
Remyelination; multiple sclerosis; IgM; EAE; immunomodulation;
D O I
10.1016/j.jneuroim.2003.11.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A set of antibodies capable of binding glial cells promotes remyelination in models of multiple sclerosis (MS). Within this set, the mouse antibody, SCH94.03, was immunomodulatory implying that immune system mobilization might be integral to remyelination. We evaluated whether the human remyelination-promoting antibody rHIgM22 influences acquired immunity. The antibody did not bind to immune cells, or influence humoral immune responses, antigen presentation, T cell proliferation or cytokine production. Treatment with rHIgM22 had no effect on demyelination or virus infection in two disease models. These results demonstrate that the remyelination-promoting activity of antibody rHIgM22 is not dependent on immunomodulation. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 161
页数:9
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