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a TNO Prevention and
Health, Gaubius Laboratory, Leiden, the Netherlands, b Department of Rheumatology, University
Hospital Leiden, the Netherlands
Correspondence to: Dr Rijken, TNO Prevention and Health, Gaubius Laboratory, PO Box 2215, 2301 CE Leiden, the Netherlands
Accepted for publication 22 November 1999
BACKGROUND
Excessive
fibrin deposition within the inflamed joints of rheumatoid arthritis
(RA) patients suggests that local fibrinolysis is inefficient, which
seems to be in contrast with the observed increased levels of urokinase
type plasminogen activator (u-PA). Thrombin-mediated inactivation of
single chain u-PA (scu-PA) into an inactive form called
thrombin-cleaved two chain u-PA (tcu-PA/T) may provide a possible
explanation for this contradiction.
AIM
To assess the
occurrence of tcu-PA/T in the synovial fluid of patients with RA and
with osteoarthritis (OA), and in the synovial fluid of controls to find
support for thrombin-mediated inactivation of scu-PA in RA.
METHODS
Levels of
scu-PA and tcu-PA/T were measured in the synovial fluid of 20 RA
patients, nine OA patients and 14 controls using sensitive
bioimmunoassays. Total urokinase antigen was quantified by a urokinase ELISA.
RESULTS
tcu-PA/T was
found in the synovial fluid of all RA and OA patients. Only in seven of
14 control samples, levels of tcu-PA/T could be measured above the
detection limit of the assay (0.2 ng/ml). The concentrations of
tcu-PA/T, scu-PA and u-PA:Ag were significantly higher in the synovial
fluid of the RA and OA patients as compared with the controls, while
the RA patients had significantly higher levels of tcu-PA/T and u-PA:Ag
than the OA patients. In RA, tcu-PA/T seemed to account for more than
40% of total urokinase antigen, while the contribution of tcu-PA/T to
total urokinase antigen was only minor in OA and the controls (9.0%
and 6.6%, respectively).
CONCLUSION
A
significant part of the high total urokinase antigen in the synovial
fluid of RA patients can be attributed to tcu-PA/T, implying that a
large amount of scu-PA is not available for fibrinolysis because of its
inactivation by thrombin. Thus, thrombin may promote the inflammation
process in RA by inhibiting the fibrinolytic system and preventing the
removal of fibrin.
This article has been cited by other articles:
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O Sanchez-Pernaute, R Largo, E Calvo, M A Alvarez-Soria, J Egido, and G Herrero-Beaumont A fibrin based model for rheumatoid synovitis Ann Rheum Dis, December 1, 2003; 62(12): 1135 - 1138. [Abstract] [Full Text] [PDF] |
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