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Journal article

A role for VAV1 in experimental autoimmune encephalomyelitis and multiple sclerosis.

Abstract:
Multiple sclerosis, the most common cause of progressive neurological disability in young adults, is a chronic inflammatory disease. There is solid evidence for a genetic influence in multiple sclerosis, and deciphering the causative genes could reveal key pathways influencing the disease. A genome region on rat chromosome 9 regulates experimental autoimmune encephalomyelitis, a model for multiple sclerosis. Using interval-specific congenic rat lines and association of single-nucleotide polymorphisms with inflammatory phenotypes, we localized the gene of influence to Vav1, which codes for a signal-transducing protein in leukocytes. Analysis of seven human cohorts (12,735 individuals) demonstrated an association of rs2546133-rs2617822 haplotypes in the first VAV1 intron with multiple sclerosis (CA: odds ratio, 1.18; CG: odds ratio, 0.86; TG: odds ratio, 0.90). The risk CA haplotype also predisposed for higher VAV1 messenger RNA expression. VAV1 expression was increased in individuals with multiple sclerosis and correlated with tumor necrosis factor and interferon-gamma expression in peripheral blood and cerebrospinal fluid cells. We conclude that VAV1 plays a central role in controlling central nervous system immune-mediated disease and proinflammatory cytokine production critical for disease pathogenesis.
Publication status:
Published

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Publisher copy:
10.1126/scitranslmed.3000278

Authors


Publisher:
American Association for the Advancement of Science
Journal:
Science translational medicine More from this journal
Volume:
1
Issue:
10
Pages:
10ra21
Publication date:
2009-12-01
DOI:
EISSN:
1946-6242
ISSN:
1946-6234


Language:
English
Keywords:
Pubs id:
pubs:52619
UUID:
uuid:10de1ae2-4213-4e86-8d18-9d5b9576157c
Local pid:
pubs:52619
Source identifiers:
52619
Deposit date:
2012-12-19
ARK identifier:

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