Assessment of rituximab's immunomodulatory synovial effects (ARISE trial). 1: clinical and synovial biomarker results

被引:139
作者
Kavanaugh, A. [1 ]
Rosengren, S. [1 ]
Lee, S. J. [1 ]
Hammaker, D. [1 ]
Firestein, G. S. [1 ]
Kalunian, K. [1 ]
Wei, N. [2 ]
Boyle, D. L. [1 ]
机构
[1] Univ Calif San Diego, Div Rheumatol Allergy & Immunol, La Jolla, CA 92093 USA
[2] Arthritis & Osteoporosis Ctr Maryland, Fredericksburg, MD USA
关键词
D O I
10.1136/ard.2007.074229
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective: Treatment with the anti-CD20 monoclonal antibody (mAb) rituximab is effective in rheumatoid arthritis (RA). Marked depletion of circulating B cells, seen in almost all patients, does not correlate with efficacy. The potential synovial immunomodulatory effects of rituximab have not been fully defined. Methods: The ARISE trial is an open label, serial synovial biopsy (pre-treatment and 8 weeks) study of rituximab, given 1 g intravenously on days 0 and 14 without peri-infusional steroids, in active RA patients on concomitant methotrexate (MTX). Synovial tissue was analysed by immunohistochemistry with digital image analysis and gene expression by real-time PCR. Results: The mean (SD) baseline DAS28 score was 6.5 (0.4), and mean MTX dose 17.3 mg/week. Of 13 patients, 11 had failed prior tumour necrosis factor (TNF) inhibitor therapy. With treatment, all patients experienced near complete depletion of circulating B cell numbers. During the 6 months after treatment, 7/13 patients achieved an American College of Rheumatology (ACR) 20% improvement (ACR20) response, 3/13 an ACR50 response and 2/13 an ACR70 response. There was a significant decrease in synovial B cells after treatment, but only a small trend towards greater reduction among clinical responders. Among the three patients with ACR50 responses there was a significant decrease in synovial immunoglobulin synthesis. Conclusions: These data suggest that unlike those in circulation, synovial B cells are decreased but are not eliminated by rituximab therapy. Patients with higher levels of response may have more consistent depletion of synovial B cells, and may also have an alteration in synovial B cell function, as indicated by decreases in synovial immunoglobulin synthesis. Thus, effects on synovial B cells may be necessary but not sufficient for inducing clinical efficacy. Other effects, such as on primary lymph organ B cell antigen presentation or cytokine production, may be operative.
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收藏
页码:402 / 408
页数:7
相关论文
共 17 条
[1]
THE CASE FOR CONFIDENCE-INTERVALS IN CONTROLLED CLINICAL-TRIALS [J].
BORENSTEIN, M .
CONTROLLED CLINICAL TRIALS, 1994, 15 (05) :411-428
[2]
Quantitative biomarker analysis of synovial gene expression by real-time PCR [J].
Boyle, DL ;
Rosengren, S ;
Bugbee, W ;
Kavanaugh, A ;
Firestein, GS .
ARTHRITIS RESEARCH & THERAPY, 2003, 5 (06) :R352-R360
[3]
Circulating levels of B lymphocyte stimulator in patients with rheumatoid arthritis following rituximab treatment - Relationships with B cell depletion, circulating antibodies, and clinical relapse [J].
Cambridge, G ;
Stohl, W ;
Leandro, MJ ;
Migone, TS ;
Hilbert, DM ;
Edwards, JCW .
ARTHRITIS AND RHEUMATISM, 2006, 54 (03) :723-732
[4]
Rituximab for rheumatoid arthritis refractory to anti-tumor necrosis factor therapy - Results of a multicenter, randomized, double-blind, placebo-controlled, phase III trial evaluating primary efficacy and safety at twenty-four weeks [J].
Cohen, Stanley B. ;
Emery, Paul ;
Greenwald, Maria W. ;
Dougados, Maxime ;
Furie, Richard A. ;
Genovese, Mark C. ;
Keystone, Edward C. ;
Loveless, James E. ;
Burmester, Gerd-Ruediger ;
Cravets, Matthew W. ;
Hessey, Eva W. ;
Shaw, Timothy ;
Totoritis, Mark C. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (09) :2793-2806
[5]
B-cell targeting in rheumatoid arthritis and other autoimmune diseases [J].
Edwards, JCW ;
Cambridge, G .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (05) :394-403
[6]
Sustained improvement in rheumatoid arthritis following a protocol designed to deplete B lymphocytes [J].
Edwards, JCW ;
Cambridge, G .
RHEUMATOLOGY, 2001, 40 (02) :205-211
[7]
Edwards JCW, 1999, IMMUNOLOGY, V97, P188
[8]
Efficacy of B-cell-targeted therapy with rituximab in patients with rheumatoid arthritis [J].
Edwards, JCW ;
Szczepanski, L ;
Szechinski, J ;
Filipowicz-Sosnowska, A ;
Emery, P ;
Close, DR ;
Stevens, RM ;
Shaw, T .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (25) :2572-2581
[9]
The efficacy and safety of rituximab in patients with active rheumatoid arthritis despite methotrexate treatment - Results of a phase IIb randomized, double-blind, placebo-controlled, dose-ranging trial [J].
Emery, P ;
Fleischmann, R ;
Filipowicz-Sosnowska, A ;
Schechtman, J ;
Szczepanski, L ;
Kavanaugh, A ;
Racewicz, AJ ;
Van Vollenhoven, RF ;
Li, NF ;
Agarwal, S ;
Hessey, EW ;
Shaw, TM .
ARTHRITIS AND RHEUMATISM, 2006, 54 (05) :1390-1400
[10]
Importance of cellular microenvironment and circulatory dynamics in B cell immunotherapy [J].
Gong, Q ;
Ou, QL ;
Ye, SM ;
Lee, WP ;
Cornelius, J ;
Diehl, L ;
Lin, WY ;
Hu, ZL ;
Lu, YM ;
Chen, YM ;
Wu, Y ;
Meng, YG ;
Gribling, P ;
Lin, ZH ;
Nguyen, K ;
Tran, T ;
Zhang, YF ;
Rosen, H ;
Martin, F ;
Chan, AC .
JOURNAL OF IMMUNOLOGY, 2005, 174 (02) :817-826