Comment on alemtuzumab and inclusion body myositis.

نویسنده

  • Steven A Greenberg
چکیده

Sir, The recent Brain publication (Dalakas et al., 2009) describing a clinical study of alemtuzumab in patients with inclusion body myositis nicely demonstrates the feasibility of enrolling and following a cohort of these patients over a long period of time as participants in an intervention study. The authors state that ‘in [inclusion body myositis] one series of alemtuzumab infusions can slow down disease progression up to 6 months’. Prior to publication of this paper in Brain, two scientific meeting abstracts and an editorial similarly reported results of this study as showing that, in inclusion body myositis, alemtuzumab may have a role in improving the clinical condition of patients (Dalakas et al., 2007a, b; Dalakas, 2008). Based on the Methods and Results now published in Brain, I have concerns that these conclusions may require further analysis for several reasons.

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منابع مشابه

LETTER TO THE EDITOR Comment on alemtuzumab and inclusion body myositis

Sir, The recent Brain publication (Dalakas et al., 2009) describing a clinical study of alemtuzumab in patients with inclusion body myositis nicely demonstrates the feasibility of enrolling and following a cohort of these patients over a long period of time as participants in an intervention study. The authors state that ‘in [inclusion body myositis] one series of alemtuzumab infusions can slow...

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LETTER TO THE EDITOR Reply to: Comment on alemtuzumab and inclusion body myositis

Sir, Dr Greenberg misinterprets several important aspects of our study, including the scope and applied methodology. Below we have addressed the points raised in his correspondence. This was a proof-of principle molecular clinicopathological study designed to investigate the effect of alemtuzumab on endomysial T cells and disease progression; it was not primarily a trial of clinical efficacy. A...

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LETTER TO THE EDITOR Reply: Comment on alemtuzumab and inclusion body myositis

Sir, Dr Greenberg misinterprets several important aspects of our study, including the scope and applied methodology. Below we have addressed the points raised in his correspondence. This was a proof-of principle molecular clinicopathological study designed to investigate the effect of alemtuzumab on endomysial T cells and disease progression; it was not primarily a trial of clinical efficacy. A...

متن کامل

Reply: Comment on alemtuzumab and inclusion body myositis

Sir, Dr Greenberg misinterprets several important aspects of our study, including the scope and applied methodology. Below we have addressed the points raised in his correspondence. This was a proof-of principle molecular clinicopathological study designed to investigate the effect of alemtuzumab on endomysial T cells and disease progression; it was not primarily a trial of clinical efficacy. A...

متن کامل

Update on treatment of inclusion body myositis.

Degenerative mechanisms such as protein accumulation and vacuolar transformation in the skeletal muscle distinguish inclusion body myositis (IBM) from other inflammatory myopathies. IBM is particularly common in patients over the age of 50 years and inevitably leads to progressive muscle weakness and atrophy. Conventional immunotherapies, albeit effective in other forms of myositis, seem to hav...

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عنوان ژورنال:
  • Brain : a journal of neurology

دوره 133 Pt 5  شماره 

صفحات  -

تاریخ انتشار 2010