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The prevalence and clinical significance of autoantibodies to plasminogen activator inhibitor 1 in systemic lupus erythematosus.
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| Title: | The prevalence and clinical significance of autoantibodies to plasminogen activator inhibitor 1 in systemic lupus erythematosus. |
| Authors: | Bates, Ruth L. Payne, Sarah J. Drury, S.L. Nelson, Paul N. Isenberg, D.A. Murphy, John J. Frampton, Geoffrey |
| Citation: | Lupus 2003, 12(8): 617-622 |
| Publisher: | SAGE Publications |
| Issue Date: | 2003 |
| URI: | http://hdl.handle.net/2436/14650 |
| DOI: | 10.1191/0961203303lu436oa |
| PubMed ID: | 12945721 |
| Additional Links: | http://lup.sagepub.com/cgi/content/abstract/12/8/617 http://direct.bl.uk/bld/PlaceOrder.do?UIN=136076849&ETOC=RN&from=searchengine |
| Abstract: | We have recently described the novel autoantigen plasminogen activator inhibitor (PAI-1) in systemic lupus erythematosus (SLE). The aim of this study was to determine the prevalence and clinical significance of anti-PAI-1 autoantibodies in patients with SLE. Autoantibodies to recombinant PAI-1 were measured in retrospective sera of 48 lupus patients by immunoassay in order to assess their clinical significance. This showed that 71% of sera from 48 lupus patients had significantly elevated anti-PAI-1 autoantibodies as compared with normal control subjects (P < 0.0001). There was a weak but significant (P < 0.043) correlation with anti-dsDNA autoantibodies. In longitudinal studies, autoantibodies against PAI-1 correlated with clinical parameters measured by the BILAG disease activity index including global clinical score. Our study demonstrates the high frequency of novel autoantibodies to PAI-1 in patients with lupus. The serial clinical correlations with anti-PAI-1 autoantibodies also support the hypothesis that these autoantibodies may play a pathogenic role in lupus. |
| Type: | Article |
| Language: | en |
| Description: | Metadata record only |
| Keywords: | Systemic lupus erythematosus Autoantigen SLE Anti-PAI-1 |
| ISSN: | 0961-2033 |
| Appears in Collections: | Molecular Immunology Research Group
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