Abstract
Interferon beta-1a (IFNâ-1a) has demonstrated efficacy in multiple sclerosis (MS), although its mechanism of action remains only partly understood. We evaluated the ex vivo and in vitro effects of IFNâ-1a (Rebif) on regulatory T-cell (T(Reg)) function in 22 relapsing-remitting MS patients and 16 healthy controls. T(Reg) function was significantly enhanced after 3 and 6 months of IFNbeta-1a therapy. Furthermore, there was a trend towards increasing proportions of total CD4(+)CD25(+) and CD4(+)CD25(+)GITR(+) T(Reg) after 6 months of IFNbeta-1a therapy when compared with baseline. In conclusion, IFNbeta-1a therapy enhances T(Reg) function, and this may be relevant in the inflammatory environment of MS lesions.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adjuvants, Immunologic / therapeutic use*
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Adult
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CD4-Positive T-Lymphocytes / metabolism
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Cohort Studies
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Female
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Glucocorticoid-Induced TNFR-Related Protein
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Humans
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In Vitro Techniques
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Interferon beta-1a
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Interferon-beta / therapeutic use*
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Interleukin-2 Receptor alpha Subunit / metabolism
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Longitudinal Studies
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Male
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Middle Aged
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Multiple Sclerosis, Relapsing-Remitting / blood
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Multiple Sclerosis, Relapsing-Remitting / drug therapy*
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Multiple Sclerosis, Relapsing-Remitting / immunology*
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Multiple Sclerosis, Relapsing-Remitting / metabolism
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Receptors, Nerve Growth Factor / metabolism
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Receptors, Tumor Necrosis Factor / metabolism
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T-Lymphocyte Subsets / pathology
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T-Lymphocytes, Regulatory / immunology*
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Treatment Outcome
Substances
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Adjuvants, Immunologic
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Glucocorticoid-Induced TNFR-Related Protein
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Interleukin-2 Receptor alpha Subunit
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Receptors, Nerve Growth Factor
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Receptors, Tumor Necrosis Factor
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TNFRSF18 protein, human
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Interferon-beta
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Interferon beta-1a