Chemokine receptor CCR5 in interferon-treated multiple sclerosis
pmid: 17511851
Chemokine receptor CCR5 in interferon-treated multiple sclerosis
To study the relationship between CC chemokine receptor CCR5 expression and disease activity in multiple sclerosis (MS) patients treated with beta-interferon (IFN-beta).The CCR5 Delta32 allele and a CCR5 promoter polymorphism associated with cell surface expression of CCR5 were analyzed in 109 patients with relapsing-remitting MS treated with IFN-beta who were followed clinically for 1 year. Cellular CCR5 expression was measured by flow cytometry.Patients with MS had a higher percentage of CCR5-positive monocytes than healthy controls. Increased monocyte expression of CCR5 correlated weakly with an increased short-term relapse risk but there was no relationship between CCR5 Delta32 allele and CCR5 promoter polymorphism genotypes and relapse risk.The results do not support a major role of CCR5 in the pathogenesis of relapses in MS patients treated with IFN-beta, but it is possible that monocyte CCR5 expression may be used as a marker of disease activity.
- Hvidovre Hospital Denmark
- Copenhagen University Hospital Denmark
- University of Copenhagen Denmark
- Rigshospitalet Denmark
- Glostrup Hospital Denmark
Adult, Central Nervous System, Genetic Markers, Male, Multiple Sclerosis, Genotype, DNA Mutational Analysis, Relapsing-Remitting, Monocytes, Promoter Regions, Multiple Sclerosis, Relapsing-Remitting, Genetic, Gene Frequency, Receptors, Humans, Genetic Predisposition to Disease, Genetic Testing, Polymorphism, Promoter Regions, Genetic, Polymorphism, Genetic, Interferon-beta, Middle Aged, Mutation, Biological Markers, Female, Interferons, CCR5, Biomarkers
Adult, Central Nervous System, Genetic Markers, Male, Multiple Sclerosis, Genotype, DNA Mutational Analysis, Relapsing-Remitting, Monocytes, Promoter Regions, Multiple Sclerosis, Relapsing-Remitting, Genetic, Gene Frequency, Receptors, Humans, Genetic Predisposition to Disease, Genetic Testing, Polymorphism, Promoter Regions, Genetic, Polymorphism, Genetic, Interferon-beta, Middle Aged, Mutation, Biological Markers, Female, Interferons, CCR5, Biomarkers
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