Volume 87, Issue 6 pp. 457-460
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Effects of recombinant α-2b-interferon therapy in patients with progressive MS

E. Kinnunen

Corresponding Author

E. Kinnunen

Departments of Neurology, Hyvinkää Hospital, Helsinki, Finland

Department of Neurology, Hyvinkää Hospital, Sairaalankatu 1, 05850 Hyvinkää, FinlandSearch for more papers by this author
T. Timonen

T. Timonen

Departments of Pathology, University of Helsinki, Helsinki, Finland

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T. Pirttilä

T. Pirttilä

Departments of Neurology, University of Tampere, Helsinki, Finland

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P. Kalliomäki

P. Kalliomäki

Departments of Pathology, University of Helsinki, Helsinki, Finland

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L. Ketonen

L. Ketonen

Departments of Diagnostic Radiology, Strong Memorial Hospital, Rochester, U.S.A., Helsinki, Finland

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E. Matikainen

E. Matikainen

Departments of Institute of Occupational Health, Helsinki, Helsinki, Finland

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R. Sepponen

R. Sepponen

Departments of Instrumentarium Corp., Helsinki, Finland

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J. Juntunen

J. Juntunen

Departments of Institute of Occupational Health, Helsinki, Helsinki, Finland

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First published: June 1993
Citations: 18

Abstract

The effects of systemic recombinant interferon-α-2b were studied in 6 carefully selected patients with progressive multiple sclerosis. 3.0 million IU were given as daily subcutaneous injections for 6 months, 5 patients showed worsening disability, and in 4 of them new or enlarged lesions were detected in MRI. In one patient no change in disability was found; his MRI showed regressed changes. The mean progression index during the treatment was significantly higher (p < 0.02) than during the previous 2 to 3 years’ period of continuous progression. The frequency of peripheral blood natural killer (CD16 +) cells declined significantly 3 months during the treatment, but returned to the pretreatment values after termination the treatment. An increase of intrathecal IgG synthesis and oligoclonal bands was demonstrated in 4 and 3 patients, respectively. Our experience suggests that long-term recombinant IFN-α-2b treatment may activate the immunological process of MS.

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