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Interferon-beta 1b treatment modulates cytokines in patients with primary progressive multiple sclerosis
ISSN
0001-6314
Date Issued
2006
Author(s)
Dressel, Alexander
Kolb, A. K.
Elitok, E.
Bitsch, Annette
Bogumil, T.
Weber, F.
DOI
10.1111/j.1600-0404.2006.00700.x
Abstract
Objectives - It is unknown whether the immunological effects of binterferon (IFN-beta) differ in primary progressive multiple sclerosis (PPMS) when compared with relapsing - remitting multiple sclerosis (RRMS). Therefore, we investigated the effects of IFN-beta 1b treatment in PPMS on proliferation and cytokine pattern of peripheral blood mononuclear cells (PBMC) and interleukin-10 (IL-10) serum level. Methods - Eighteen patients were treated with IFN-b1b for 12 months in an open-label trial. Serum and PBMC were collected longitudinally. Results - Interleukin-10 serum levels increased ( P 0.02) during treatment. Tumor necrosis factor-alpha was increased in anti CD3 (OKT3) antibody stimulated PBMC during treatment (P = 0.04), whereas secretion of IL-10 was decreased in OKT3 ( P 0.04), but increased in concavalin A stimulated PBMC ( P 0.02). Conclusions - Interleukin-10 serum levels rose in IFN-b1 beta-treated patients as has been observed in RRMS. The changes in cytokine patterns secreted by T-lymphocytes of PPMS patients, however, differ from effects observed in RRMS supporting the hypothesis that PPMS differs in some immunological aspects from RRMS.