Literature DB >> 18164542

The therapy of multiple sclerosis with immune-modulating or immunosuppressive drug. A critical evaluation based upon evidence based parameters and published systematic reviews.

Marinella Clerico1, Chiara Rivoiro, Giulia Contessa, Daniela Viglietti, Luca Durelli.   

Abstract

Today many different drugs are available for treatment of multiple sclerosis (MS). Interferons, glatiramer acetate, mitoxantrone, and natalizumab have been approved by the regulatory authorities of many countries for the treatment of MS. Evidence based medicine (EBM) principles allow physicians to better address the correct treatment for patients. This article aimed to review all the clinical trials on immune-modulating and immunosuppressive drugs on the basis of the EBM principles. Based on the evidence to date interferon beta represents the best therapeutic option, particularly if given at high doses and with multiple injections per week. Due to its lower efficacy, glatiramer acetate should be used as a second choice in case of intolerable side effects or toxicity of interferon beta. Great efficacy has been demonstrated for mitoxantrone and natalizumab. These drugs should be, however, used with particular attention for their potential toxic effects.

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Year:  2008        PMID: 18164542     DOI: 10.1016/j.clineuro.2007.10.020

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  8 in total

Review 1.  Opportunistic autoimmune disorders: from immunotherapy to immune dysregulation.

Authors:  Yi-chi M Kong; Wei-Zen Wei; Yaron Tomer
Journal:  Ann N Y Acad Sci       Date:  2010-01       Impact factor: 5.691

Review 2.  [Intravenous immunoglobulins in multiple sclerosis. An update].

Authors:  S Schwarz; H-M Meinck; B Storch-Hagenlocher
Journal:  Nervenarzt       Date:  2009-08       Impact factor: 1.214

3.  Cooperative contributions of interferon regulatory factor 1 (IRF1) and IRF8 to interferon-γ-mediated cytotoxic effects on oligodendroglial progenitor cells.

Authors:  Makoto Horiuchi; Aki Itoh; David Pleasure; Keiko Ozato; Takayuki Itoh
Journal:  J Neuroinflammation       Date:  2011-01-24       Impact factor: 8.322

Review 4.  Mitoxantrone: benefits and risks in multiple sclerosis patients.

Authors:  V Martinelli; M Radaelli; L Straffi; M Rodegher; G Comi
Journal:  Neurol Sci       Date:  2009-10       Impact factor: 3.307

5.  Interferon-triggered transcriptional cascades in the oligodendroglial lineage: a comparison of induction of MHC class II antigen between oligodendroglial progenitor cells and mature oligodendrocytes.

Authors:  Takayuki Itoh; Makoto Horiuchi; Aki Itoh
Journal:  J Neuroimmunol       Date:  2009-05-20       Impact factor: 3.478

6.  Clinical efficacy issues in the treatment of multiple sclerosis: update of natalizumab.

Authors:  Francesco Patti; Angelo Pappalardo
Journal:  Clinicoecon Outcomes Res       Date:  2009-08-21

7.  Delayed nerve stimulation promotes axon-protective neurofilament phosphorylation, accelerates immune cell clearance and enhances remyelination in vivo in focally demyelinated nerves.

Authors:  Nikki A McLean; Bogdan F Popescu; Tessa Gordon; Douglas W Zochodne; Valerie M K Verge
Journal:  PLoS One       Date:  2014-10-13       Impact factor: 3.240

8.  Extracellular adenosine signaling induces CX3CL1 expression in the brain to promote experimental autoimmune encephalomyelitis.

Authors:  Jeffrey H Mills; Leah M Alabanza; Deeqa A Mahamed; Margaret S Bynoe
Journal:  J Neuroinflammation       Date:  2012-08-10       Impact factor: 8.322

  8 in total

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