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Article has an altmetric score of 3

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Referenced in 2 patents
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Research Article Free access | 10.1172/JCI119889

Localization of the apoptosis-inducing activity of lupus anticoagulant in an annexin V-binding antibody subset.

N Nakamura, T Ban, K Yamaji, Y Yoneda, and Y Wada

Department of Molecular Medicine, Research Institute, Osaka Medical Center for Maternal and Child Health, Izumi, Osaka 590-02, Japan.

Find articles by Nakamura, N. in: PubMed | Google Scholar

Department of Molecular Medicine, Research Institute, Osaka Medical Center for Maternal and Child Health, Izumi, Osaka 590-02, Japan.

Find articles by Ban, T. in: PubMed | Google Scholar

Department of Molecular Medicine, Research Institute, Osaka Medical Center for Maternal and Child Health, Izumi, Osaka 590-02, Japan.

Find articles by Yamaji, K. in: PubMed | Google Scholar

Department of Molecular Medicine, Research Institute, Osaka Medical Center for Maternal and Child Health, Izumi, Osaka 590-02, Japan.

Find articles by Yoneda, Y. in: PubMed | Google Scholar

Department of Molecular Medicine, Research Institute, Osaka Medical Center for Maternal and Child Health, Izumi, Osaka 590-02, Japan.

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Published May 1, 1998 - More info

Published in Volume 101, Issue 9 on May 1, 1998
J Clin Invest. 1998;101(9):1951–1959. https://doi.org/10.1172/JCI119889.
© 1998 The American Society for Clinical Investigation
Published May 1, 1998 - Version history
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Abstract

Lupus anticoagulant (LAC) is associated with arterial and venous thrombosis, thrombocytopenia, and recurrent fetal loss. We have reported previously that plasma with LAC activity induces apoptosis in endothelial cells and binds annexin V (Nakamura, N., Y. Shidara, N. Kawaguchi, C. Azuma, N. Mitsuda, S. Onishi, K. Yamaji, and Y. Wada. 1994. Biochem. Biophys. Res. Commun. 205:1488-1493). In this study, we separated two IgG antibody fractions, one with and one without affinity for annexin V, from 10 patients with LAC. LAC and apoptotic activities were localized in the annexin V-binding fraction in all 10 patients. DNA fragmentation was dose-dependent, paralleling the amount of IgG added to the human umbilical vein endothelial cell culture medium, and was inhibited by preincubation with annexin V. Removal of the antiphospholipid antibodies from patient IgG with phospholipid liposomes did not abolish the apoptosis-inducing activities or binding to annexin V. These results imply that patients with LAC often have antibodies that do not bind phospholipids and are responsible for the induction of apoptosis in endothelial cells.

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Referenced in 2 patents
17 readers on Mendeley
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