Description
Glatiramer Acetate (GA) has provided safe and effective treatment for multiple sclerosis (MS) patients  for two decades. It acts as an antigen, yet the precise mechanism of action remains to be fully  elucidated, and no validated pharmacokinetic or pharmacodynamic biomarkers exist. In order to better  characterize GAs biological impact, genome-wide expression studies were conducted with a human  monocyte (THP-1) cell line. Consistent with previous literature, branded GA upregulated antiinflammatory  markers (e.g. IL10), and modulated multiple immune-related pathways. Despite some  similarities, significant differences were observed between expression profiles induced by branded GA  and Probioglat, a differently-manufactured glatiramoid purported to be a generic GA.