Literature DB >> 21264146

Beta-interferons in multiple sclerosis.

Sourabh Aggarwal1, Vishal Sharma, Jesna S Mathew.   

Abstract

Entities:  

Year:  2010        PMID: 21264146      PMCID: PMC3021941          DOI: 10.4103/0972-2327.74189

Source DB:  PubMed          Journal:  Ann Indian Acad Neurol        ISSN: 0972-2327            Impact factor:   1.383


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Sir, We read the article “Beta-interferons in multiple sclerosis: A single center experience in India”[1] by Gupta et al. with great interest. We applaud the authors for conducting such a study in Indian setup. However, the high cost of therapy with interferon and even glatiramer acetate is a matter of concern in treatment of patients with multiple sclerosis in Indian setup. A study by Singhal et al. has concluded that mitoxantrone, which is a cheap alternative to interferon, has shown promising results in Indian setup when given as an initial therapy for the patients with multiple sclerosis[2] and could be given a try, especially when cost involved is a concern for the patients. Mitoxantrone acts due to its immunomodulatory properties by decreasing selectively the secretion of few cytokines like interferon (IFN)-γ, tumor necrosis factor-α, and IL-2.[3] Mitoxantrone has also been found to be better when used as an induction therapy followed by the use of glatiramer acetate than when glatiramer acetate was used alone in the study by Vollmer et al.[4] Although few adverse side effects were associated with the therapy by mitoxantrone like leucopenia, urinary tract infection, and mild hair loss.[2] The new emerging therapies for the treatment of multiple sclerosis include alemtuzumab, natalizumab, and autologous stem cell transplantation which have also shown promising results in trials with respect to disability improvement. A study done by Cole et al. reported reduced disability in patients treated with alemtuzumab.[5] A multicentric study carried out by Putzki et al. showed significant improvement in disability score with use of natalizumab.[6] Another study using autologous hemopoietic stem cell transplantation in relapsing–remitting MS showed significant improvements in neurological disability.[7] However, all these therapies are in preliminary stage and are associated with significant high cost which is a limiting factor in treatment of patients with multiple sclerosis in India. Nonetheless, the authors have done a commendable job in view of the patients who seriously impaired by multiple sclerosis and we appreciate their efforts.
  5 in total

1.  Glatiramer acetate after induction therapy with mitoxantrone in relapsing multiple sclerosis.

Authors:  T Vollmer; H Panitch; A Bar-Or; J Dunn; M S Freedman; S K Gazda; D Campagnolo; F Deutsch; D L Arnold
Journal:  Mult Scler       Date:  2008-04-18       Impact factor: 6.312

Review 2.  Mechanism of action of mitoxantrone.

Authors:  Edward J Fox
Journal:  Neurology       Date:  2004-12-28       Impact factor: 9.910

3.  Efficacy and safety of mitoxantrone, as an initial therapy, in multiple sclerosis: experience in an Indian tertiary care setting.

Authors:  B S Singhal; Sheth Geeta; Shilpa G Hundalani; Suresh Menon
Journal:  Neurol India       Date:  2009 Jul-Aug       Impact factor: 2.117

4.  Autologous non-myeloablative haemopoietic stem cell transplantation in relapsing-remitting multiple sclerosis: a phase I/II study.

Authors:  Richard K Burt; Yvonne Loh; Bruce Cohen; Dusan Stefoski; Dusan Stefosky; Roumen Balabanov; George Katsamakis; Yu Oyama; Eric J Russell; Jessica Stern; Paolo Muraro; John Rose; Alessandro Testori; Jurate Bucha; Borko Jovanovic; Francesca Milanetti; Jan Storek; Julio C Voltarelli; William H Burns
Journal:  Lancet Neurol       Date:  2009-01-29       Impact factor: 44.182

5.  Beta-interferons in multiple sclerosis: a single center experience in India.

Authors:  Salil Gupta; R Varadarajulu; R K Ganjoo
Journal:  Ann Indian Acad Neurol       Date:  2010-04       Impact factor: 1.383

  5 in total
  1 in total

1.  Type I IFN promotes IL-10 production from T cells to suppress Th17 cells and Th17-associated autoimmune inflammation.

Authors:  Lixia Zhang; Shunzong Yuan; Genhong Cheng; Beichu Guo
Journal:  PLoS One       Date:  2011-12-06       Impact factor: 3.240

  1 in total

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