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Research Article Free access | 10.1172/JCI115926

Lupus anticoagulant activity of autoimmune antiphospholipid antibodies is dependent upon beta 2-glycoprotein I.

R A Roubey, C W Pratt, J P Buyon, and J B Winfield

Department of Medicine, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill 27599.

Find articles by Roubey, R. in: PubMed | Google Scholar

Department of Medicine, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill 27599.

Find articles by Pratt, C. in: PubMed | Google Scholar

Department of Medicine, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill 27599.

Find articles by Buyon, J. in: PubMed | Google Scholar

Department of Medicine, Thurston Arthritis Research Center, University of North Carolina, Chapel Hill 27599.

Find articles by Winfield, J. in: PubMed | Google Scholar

Published September 1, 1992 - More info

Published in Volume 90, Issue 3 on September 1, 1992
J Clin Invest. 1992;90(3):1100–1104. https://doi.org/10.1172/JCI115926.
© 1992 The American Society for Clinical Investigation
Published September 1, 1992 - Version history
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Abstract

It has been reported that antiphospholipid autoantibodies do not recognize phospholipid alone, but rather the plasma protein beta 2-glycoprotein I (beta 2GPI), or a beta 2GPI-phospholipid complex. In vitro beta 2GPI binds to anionic phospholipids and inhibits the prothrombinase activity of procoagulant membranes. In light of the fact that lupus anticoagulants, a type of antiphospholipid antibody, have similar anticoagulant properties, the relationship of beta 2GPI to lupus anticoagulant activity was investigated. IgG from patients with autoimmune diseases or syphilis were tested for anticardiolipin reactivity and lupus anticoagulant activity in the presence and absence of beta 2GPI. As expected, anti-cardiolipin reactivity associated with autoimmune disease was beta 2GPI dependent. In contrast, IgG from a patient with syphilis recognized cardiolipin alone and binding was inhibited by beta 2GPI. Autoimmune antiphospholipid antibodies prolonged the dilute Russell viper venom time of normal plasma, but had no effect on beta 2GPI-depleted plasma. Antiphospholipid antibodies associated with syphilis had no anticoagulant effect. RP-1, an anti-beta 2GPI mAb, had anticoagulant effects similar to those of autoimmune antiphospholipid antibodies. These data demonstrate that antiphospholipid autoantibodies exert lupus anticoagulant activity via an interaction with beta 2GPI. These antibodies and RP-1 appear to amplify the anticoagulant effect of beta 2GPI itself.

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