TY - JOUR
T1 - Effect of hydroxychloroquine treatment on pro-inflammatory cytokines and disease activity in SLE patients
T2 - Data from LUMINA (LXXV), a multiethnic US cohort
AU - Willis, R.
AU - Seif, A. M.
AU - McGwin, G.
AU - Martinez-Martinez, L. A.
AU - González, E. B.
AU - Dang, N.
AU - Papalardo, E.
AU - Liu, J.
AU - Vilá, L. M.
AU - Reveille, J. D.
AU - Alarcón, G. S.
AU - Pierangeli, S. S.
N1 - Funding Information:
This work was supported by NIH (grant # T32 AR052283T32 to AMS as salary support), the National Institute of Arthritis and Musculoskeletal and Skin Disease (P01 AR49084), General Clinical Research Centers (NCRR/NIH, M01-RR02558 [UTH] and M01-RR00032 [UAB]) and the National Center for Research Resources (NCRR/HIH) RCMI Clinical Research Infrastructure Initiative (RCRII, 1P20RR11126). These studies were partially funded by resources from the Antiphospholipid Standardization Laboratory, University of Texas Medical Branch.
PY - 2012/7
Y1 - 2012/7
N2 - Objective: We sought to determine the effect of hydroxychloroquine therapy on the levels proinflammatory/prothrombotic markers and disease activity scores in patients with systemic lupus erythematosus (SLE) in a multiethnic, multi-center cohort (LUMINA). Methods: Plasma/serum samples from SLE patients (n=35) were evaluated at baseline and after hydroxychloroquine treatment. Disease activity was assessed using SLAM-R scores. Interferon (IFN)-α2, interleukin (IL)-1β, IL-6, IL-8, inducible protein (IP)-10, monocyte chemotactic protein-1, tumor necrosis factor (TNF)-α and soluble CD40 ligand (sCD40L) levels were determined by a multiplex immunoassay. Anticardiolipin antibodies were evaluated using ELISA assays. Thirty-two frequency-matched plasma/serum samples from healthy donors were used as controls. Results: Levels of IL-6, IP-10, sCD40L, IFN-α and TNF-α were significantly elevated in SLE patients versus controls. There was a positive but moderate correlation between SLAM-R scores at baseline and levels of IFN-α (p=0.0546). Hydroxychloroquine therapy resulted in a significant decrease in SLAM-R scores (p=0.0157), and the decrease in SLAM-R after hydroxychloroquine therapy strongly correlated with decreases in IFN-α (p=0.0087). Conclusions: Hydroxychloroquine therapy resulted in significant clinical improvement in SLE patients, which strongly correlated with reductions in IFN-α levels. This indicates an important role for the inhibition of endogenous TLR activation in the action of hydroxychloroquine in SLE and provides additional evidence for the importance of type I interferons in the pathogenesis of SLE. This study underscores the use of hydroxychloroquine in the treatment of SLE.
AB - Objective: We sought to determine the effect of hydroxychloroquine therapy on the levels proinflammatory/prothrombotic markers and disease activity scores in patients with systemic lupus erythematosus (SLE) in a multiethnic, multi-center cohort (LUMINA). Methods: Plasma/serum samples from SLE patients (n=35) were evaluated at baseline and after hydroxychloroquine treatment. Disease activity was assessed using SLAM-R scores. Interferon (IFN)-α2, interleukin (IL)-1β, IL-6, IL-8, inducible protein (IP)-10, monocyte chemotactic protein-1, tumor necrosis factor (TNF)-α and soluble CD40 ligand (sCD40L) levels were determined by a multiplex immunoassay. Anticardiolipin antibodies were evaluated using ELISA assays. Thirty-two frequency-matched plasma/serum samples from healthy donors were used as controls. Results: Levels of IL-6, IP-10, sCD40L, IFN-α and TNF-α were significantly elevated in SLE patients versus controls. There was a positive but moderate correlation between SLAM-R scores at baseline and levels of IFN-α (p=0.0546). Hydroxychloroquine therapy resulted in a significant decrease in SLAM-R scores (p=0.0157), and the decrease in SLAM-R after hydroxychloroquine therapy strongly correlated with decreases in IFN-α (p=0.0087). Conclusions: Hydroxychloroquine therapy resulted in significant clinical improvement in SLE patients, which strongly correlated with reductions in IFN-α levels. This indicates an important role for the inhibition of endogenous TLR activation in the action of hydroxychloroquine in SLE and provides additional evidence for the importance of type I interferons in the pathogenesis of SLE. This study underscores the use of hydroxychloroquine in the treatment of SLE.
KW - Lupus
KW - biomarkers of inflammation
KW - biomarkers of thrombosis
KW - hydroxychloroquine
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U2 - 10.1177/0961203312437270
DO - 10.1177/0961203312437270
M3 - Article
C2 - 22343096
AN - SCOPUS:84861835445
SN - 0961-2033
VL - 21
SP - 830
EP - 835
JO - Lupus
JF - Lupus
IS - 8
ER -