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Autoimmune MRL mice express high-affinity IgG2b monoclonal autoantibodies to heparin.

作者信息

Fillit H, Edstrom W, Yang C P, Moran T, Dimitriu-Bona A

机构信息

The Henry L. Schwartz Department of Geriatrics and Adult Development, The Mount Sinai Medical Center, New York, New York 10029-6574, USA.

出版信息

Clin Immunol Immunopathol. 1996 Oct;81(1):62-7. doi: 10.1006/clin.1996.0158.

DOI:10.1006/clin.1996.0158
PMID:8808643
Abstract

Heparin and heparan sulfate are related glycosaminoglycans which demonstrate high-affinity interactions with a number of proteins, including antithrombin III. The immunogenicity of heparin has been reported previously employing heparin-protein conjugates as immunogens and as antigens in solid-phase assays. Previous studies also demonstrate that anti-heparin antibodies play a role in autoimmune diseases including systemic lupus and anti-phospholipid syndrome and in patients who receive heparin for therapeutic purposes. In the current study, we investigated the expression of monoclonal anti-heparin antibodies in nonimmunized, autoimmune MRL/lpr/lpr++ mice employing a liquid-phase radioimmunoassay. The Kd of monoclonal IgG2b autoantibodies for heparin was approximately 10(-8)M. Anti-heparin antibodies were precipitating, and were not polyreactive. The IgG monoclonal antibodies described in this study represent an immunological instance of a specific, high-affinity heparin-protein interaction.

摘要

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