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pubmed-article:11063837pubmed:abstractTextEffects on adhesion molecules of immune cells might contribute to the mode of action of interferon-beta (IFN-beta) in multiple sclerosis (MS). We have serially monitored the cell surface expression of integrins CD49d (VLA-4) and CD11a (LFA-1) on fresh T lymphocyte subpopulations from 5 MS patients monthly for 2 months prior to treatment and for 3 months on treatment with IFN-beta1b. In parallel, we assessed inflammatory disease activity by monthly contrast-enhanced magnetic resonance imaging (MRI). IFN-beta treatment specifically downregulated CD49d expression on CD8+ and CD4+/CD45RO+ 'memory' T lymphocytes and differentially modulated the proportion of CD4+, CD8+ and CD27+ T cells. These effects may play an important role in the reduction of central nervous system cell trafficking and inflammation in MS.lld:pubmed
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pubmed-article:11063837pubmed:articleTitleVLA-4/CD49d downregulated on primed T lymphocytes during interferon-beta therapy in multiple sclerosis.lld:pubmed
pubmed-article:11063837pubmed:affiliationNeuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, 10 Center Drive MSC1400, 20892-1400, Bethesda, MD, USA. pmuraro@umich.itlld:pubmed
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