Journal
EXPERIMENTAL AND MOLECULAR PATHOLOGY
Volume 99, Issue 3, Pages 498-505Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yexmp.2015.09.007
Keywords
RGC-32; Multiple sclerosis; Glatiramer acetate; Biomarker; FasL; IL-21
Categories
Funding
- Teva Neuroscience grant [CNS-2014-175]
- Veterans Administration Merit Award [BX001458]
- Foundation of the Consortium of Multiple Sclerosis Centers' MS Workforce of the Future program
- University of Maryland School of Medicine Office of Student Research
- Leslie B. Barnett Memorial Student Fellowship
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Currently there is critical need for the identification of reliable biomarkers to help guide clinical management of multiple sclerosis (MS) patients. We investigated the combined roles of Response Gene to Complement 32 (RGC-32), FasL, CDC2, AKT, and IL-21 as possible biomarkers of relapse and response to glatiramer acetate (GA) treatment in relapsing-remitting MS (RRMS) patients. Over the course of 2 years, a cohort of 15 GA-treated RRMS patients was clinically monitored and peripheral blood mononuclear cells (PBMCs) were collected at 0,3, 6, and 12 months. Target gene mRNA expression was measured in patients' isolated PBMCs by real-time qRT-PCR. Compared to stable MS patients, those with acute relapses exhibited decreased expression of RGC-32 (p < 0.0001) and FasL (p < 0.0001), increased expression of IL-21 (p = 0.04), but no change in CDC2 or AKT. Compared to non-responders, responders to GA treatment showed increased expression of RGC-32 (p < 0.0001) and FasL (p < 0.0001), and decreased expression of IL-21 (p = 0.02). Receiver operating characteristic (ROC) analysis was used to assess the predictive accuracy of each putative biomarker. The probability of accurately detecting relapse was 90% for RGC-32, 88% for FasL, and 75% for IL-21. The probability of accurately detecting response to GA was 85% for RGC-32, 90% for FasL, and 85% for IL-21. Our data suggest that RGC-32, FasL, and IL-21 could serve as potential biomarkers for the detection of MS relapse and response to GA therapy. (C) 2015 Elsevier Inc. All rights reserved.
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