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A rapid agglutination assay to detect anti-streptokinase antibodies
Authors:JP?McRedmond  author-information"  >  author-information__contact u-icon-before"  >  mailto:james.mcredmond@ucd.ie"   title="  james.mcredmond@ucd.ie"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,NT?Mulvihill,M?Kane,B?Burke,B?Aloul,T?Forde,M?Walsh,DJ?Fitzgerald
Affiliation:(1) Department of Clinical Pharmacology, BioResearch Ireland, National University of Ireland, Galway, Ireland;(2) Royal College of Surgeons in Ireland, Department of Cardiology, BioResearch Ireland, National University of Ireland, Galway, Ireland;(3) CResT Directorate, St James’s Hospital, National Diagnostics Centre, BioResearch Ireland, National University of Ireland, Galway, Ireland;(4) Conway Institute, University College Dublin, Belfield, Dublin 4
Abstract:Background Streptokinase resistance may cause suboptimal thrombolytic therapy. Aim To develop a rapid latex-bead assay to detect streptokinase antibodies. Methods Sera were obtained from 16 patients presenting with acute myocardial infarction (MI) before treatment with streptokinase and 1 and 6 months post treatment, and from 100 controls. Sera were assayed for anti-streptokinase antibodies using a functional streptokinase-neutralising assay. Results Streptokinase-neutralising activity was low in controls (54±5U/ml) and patients prior to treatment (101±18), increasing to 2,110±823 and 1,017±169 at 1 and 6 months (mean±SEM). The latex assay had a sensitivity of 94% and a specificity of 93% for detecting individuals with >350U/ml of streptokinase resistance, which is sufficient to neutralise the drug clinically. Conclusions Estimation of streptokinase resistance using an enzyme immunoassay and a latex bead assay correlated well with serum neutralising activity. This assay can rapidly identify patients who have a high level of streptokinase-neutralising activity.
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