Serum Gelatinases Levels in Multiple Sclerosis Patients during 21 Months of Natalizumab Therapy

Author:

Castellazzi Massimiliano1ORCID,Bellini Tiziana1,Trentini Alessandro1,Delbue Serena2,Elia Francesca2,Gastaldi Matteo3,Franciotta Diego3,Bergamaschi Roberto3,Manfrinato Maria Cristina1,Volta Carlo Alberto4,Granieri Enrico1,Fainardi Enrico5

Affiliation:

1. Department of Biomedical and Specialist Surgical Sciences, University of Ferrara, 44124 Ferrara, Italy

2. Department of Biomedical, Surgical and Dental Sciences, University of Milano, 20133 Milano, Italy

3. Department of General Neurology, National Neurological Institute C. Mondino, 27100 Pavia, Italy

4. Department of Morphology, Experimental Medicine and Surgery, University of Ferrara, 44124 Ferrara, Italy

5. Department of Neurosciences and Rehabilitation, S. Anna Hospital, 44124 Ferrara, Italy

Abstract

Background. Natalizumab is a highly effective treatment approved for multiple sclerosis (MS). The opening of the blood-brain barrier mediated by matrix metalloproteinases (MMPs) is considered a crucial step in MS pathogenesis. Our goal was to verify the utility of serum levels of active MMP-2 and MMP-9 as biomarkers in twenty MS patients treated with Natalizumab.Methods. Serum levels of active MMP-2 and MMP-9 and of specific tissue inhibitors TIMP-1 and TIMP-2 were determined before treatment and for 21 months of therapy.Results. Serum levels of active MMP-2 and MMP-9 and of TIMP-1 and TIMP-2 did not differ during the treatment. The ratio between MMP-9 and MMP-2 was increased at the 15th month compared with the 3rd, 6th, and 9th months, greater at the 18th month than at the 3rd and 6th months, and higher at the 21st than at the 3rd and 6th months.Discussion. Our data indicate that an imbalance between active MMP-9 and active MMP-2 can occur in MS patients after 15 months of Natalizumab therapy; however, they do not support the use of serum active MMP-2 and active MMP-9 and TIMP-1 and TIMP-2 levels as biomarkers for monitoring therapeutic response to Natalizumab.

Publisher

Hindawi Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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