Autologous stem cell transplantation as rescue therapy in malignant forms of multiple sclerosis

Author:

Mancardi Giovanni Luigi1,Murialdo Alessandra2,Rossi Paolo3,Gualandi Francesca4,Martino Gianvito3,Marmont Alberto4,Ciceri Fabio5,Schenone Angelo6,Parodi Roberto Carlo7,Capello Elisabetta2,Comi Giancarlo3,Uccelli Antonio6

Affiliation:

1. Department of Neurosciences, Ophthalmology and Genetics, University of Genoa, Genoa, Italy, Centre of Excellence for Biomedical Research, University of Genoa, Genoa, Italy,

2. Department of Neurosciences, Ophthalmology and Genetics, University of Genoa, Genoa, Italy

3. Department of Neurology and Clinical Neurophysiology, University Vita-Salute San Raffaele, Milan, Italy

4. II Division of Haematology and Stem Cell Transplantation Centre, S. Martino Hospital, Genoa, Italy

5. Department of Haematology, University Vita-Salute San Raffaele, Milan, Italy

6. Department of Neurosciences, Ophthalmology and Genetics, University of Genoa, Genoa, Italy, Centre of Excellence for Biomedical Research, University of Genoa, Genoa, Italy

7. Division of Neuroradiology, San Martino Hospital, Genoa, Italy

Abstract

Malignant forms of multiple sclerosis (MS) represent a limited group of very aggressive demyelinating diseases, which rapidly progress to severe disability leading often to life-threatening conditions. On these clinical entities, currently available therapies for MS are not very effective. Recently, it has been demonstrated that intense immunosuppression followed by autologous stem cell transplantation (ASCT) can affect the clinical course of individuals with severe MS and completely abrogate the inflammatory activity detected by magnetic resonance imaging (MRI). We report on the treatment with intense immune ablation followed by ASCT of three patients with malignant MS whose clinical course indicated a dramatically poor prognosis. This procedure succeeded in halting the rapidly worsening course of disease. The effect was long lasting, as demonstrated by a sustained efficacy over a two-year period in two subjects and 12 months in the third case. In addition, a striking effect on inflammation-related MRI findings was obtained. These results support a role for intense immunosuppression followed by ASCT as treatment in rapidly evolving malignant MS cases unresponsive to conventional therapies.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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