Monocyte migration to the synovium in rheumatoid arthritis patients treated with adalimumab

被引:48
作者
Herenius, M. M. J. [1 ]
Thurlings, R. M. [1 ]
Wijbrandts, C. A. [1 ]
Bennink, R. J. [2 ]
Dohmen, S. E. [3 ]
Voermans, C. [3 ]
Wouters, D. [4 ]
Izmailova, E. S. [5 ]
Gerlag, D. M. [1 ]
van Eck-Smit, B. L. F. [2 ]
Tak, P. P. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Clin Immunol & Rheumatol, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Nucl Med, NL-1100 DE Amsterdam, Netherlands
[3] Sanquin Res, Dept Expt Immunohematol, Landsteiner Lab, Amsterdam, Netherlands
[4] Sanquin Res, Dept Immunopathol, Amsterdam, Netherlands
[5] Millennium Pharmaceut Inc, Dept Res & Dev, Cambridge, MA USA
关键词
TUMOR-NECROSIS-FACTOR; ALPHA MONOCLONAL-ANTIBODY; TISSUE; BLOCKADE; JOINTS; DEACTIVATION; INFLAMMATION; ENDOTHELIUM; INITIATION; REDUCTION;
D O I
10.1136/ard.2010.141549
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives The mechanism of action of treatment with tumour necrosis factor (TNF) blockers in rheumatoid arthritis (RA) is still not completely understood. The aim of this study was to test if adalimumab treatment could affect the influx of monocytes into the synovium. Methods A novel technique was used to analyse the migration of labelled autologous monocytes before and 14 days after initiation of adalimumab treatment using scintigraphy. CD14 monocytes were isolated from patients with RA, using a positive selection procedure with magnetic-activated cell sorting, and labelled with technetium-99m-hexamethylpropylene-amino-oxime. Scintigraphic scans were made 1, 2 and 3 h after re-infusion. Results As early as 14 days after the start of treatment with adalimumab a significant decrease in disease activity score evaluated in 28 joints was shown. There was no significant decrease in the influx of monocytes into the joint at this time. Conclusions This study indicates that adalimumab treatment does not reduce the influx of monocytes into the synovium early after initiation of treatment. As previous studies showed a rapid decrease in macrophage infiltration after TNF-antibody therapy, which could not be explained by increased cell death, this points to an important role for enhanced efflux of inflammatory cells from the synovium.
引用
收藏
页码:1160 / 1162
页数:3
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