PREVENTION OF EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS BY ANTIBODIES AGAINST ALPHA-4-BETA-1 INTEGRIN

被引:1490
作者
YEDNOCK, TA
CANNON, C
FRITZ, LC
SANCHEZMADRID, F
STEINMAN, L
KARIN, N
机构
[1] UNIV AUTONOMA MADRID,MADRID 34,SPAIN
[2] STANFORD UNIV,STANFORD,CA 94305
关键词
D O I
10.1038/356063a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
EXPERIMENTAL autoimmune encephalomyelitis (EAE) is an inflammatory condition of the central nervous system with similarities to multiple sclerosis 1,2. In both diseases circulating leukocytes penetrate the blood-brain barrier and damage myelin, resulting in impaired nerve conduction and paralysis 3-5 . We sought to identify the adhesion receptors that mediate the attachment of circulating leukocytes to inflamed brain endothelium in EAE, because this interaction is the first step in leukocyte entry into the central nervous system. Using an in vitro adhesion assay on tissue sections, we found that lymphocytes and monocytes bound selectively to inflamed EAE brain vessels. Binding was inhibited by antibodies against the integrin molecule alpha-4-beta-1, but not by antibodies against numerous other adhesion receptors. When tested in vivo, anti-alpha-4 integrin effectively prevented the accumulation of leukocytes in the central nervous system and the development of EAE. Thus, therapies designed to interfere with alpha-4-beta-1 integrin may be useful in treating inflammatory diseases of the central nervous system, such as multiple sclerosis.
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页码:63 / 66
页数:4
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