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Multiple Sclerosis
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What's this?

brief-report

Daclizumab in treatment of multiple sclerosis patients

EN Ali

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

BC Healy

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

LA Stazzone

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

BA Brown

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

HL Weiner

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

SJ Khoury

Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA; Correspondence to: EN Ali, MD, Partners MS Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA. Email: eman_c5{at}yahoo.com

Background

Daclizumab is a humanized monoclonal antibody (mAb) that blocks the interleukin-2 receptor alpha subunit (IL-2R-alpha chain; CD25) expressed on activated T cells leading to the inhibition of T-cell expansion, thus strongly reduces brain inflammation in patients with multiple sclerosis (MS). Another mechanism is significant expansion of CD56 (bright) natural killer (NK) cells that in turn inhibit T-cell survival.

Objective

At the Partners MS center, we have been using Daclizumab in an open-label fashion in patients who fail first line therapy or non-standard immunosuppressive treatment. Our aim was to assess its safety and tolerability in our patient population.

Key Words: all clinical trials • daclizumab • disease modifying therapies • multiple sclerosis

This version was published on February 1, 2009

Multiple Sclerosis, Vol. 15, No. 2, 272-274 (2009)
DOI: 10.1177/1352458508097468


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