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Pregnancy Loss in the Antiphospholipid-Antibody Syndrome — A Possible Thrombogenic Mechanism

Open access
Rand, Jacob H., Wu, Xiao-Xuan, Andree, Harry A.M., Lockwood, Charles J., Guller, Seth, Scher, Jonathan, Harpel, Peter C.·1997·New England Journal of Medicine

Abstract

BACKGROUND: The mechanisms of vascular thrombosis and pregnancy loss in the antiphospholipid-antibody syndrome are unknown. Levels of annexin V, a phospholipid-binding protein with potent anticoagulant activity, are markedly reduced on placental villi from women with this syndrome. Hypercoagulability in such women may therefore be due to the reduction of surface-bound annexin V by antiphospholipid antibodies. To test this idea, we studied how antiphospholipid antibodies affect levels of annexin V on cultured trophoblasts and human umbilical-vein endothelial cells and how they affect the procoagulant activity of these cells. METHODS: We isolated IgG fractions from three patients with the antiphospholipid-antibody syndrome and from normal controls. These antibodies were incubated with cultured BeWo cells (a placental-trophoblast cell line), primary cultured trophoblasts, and human umbilical-vein endothelial cells. Annexin V on the cell surfaces was measured by an enzyme-linked immunosorbent assay. The coagulation times of plasma overlaid on the cells were also determined. RESULTS: Trophoblasts and endothelial cells exposed to antiphospholipid-antibody IgG as compared with control IgG had reduced levels of annexin V (trophoblasts, 0.37 +/- 0.02 vs. 0.85 +/- 0.12 ng per well, P=0.02; endothelial cells, 1.6 +/- 0.04 vs. 2.1 +/- 0.05 ng per well, P=0.001). Also, trophoblasts and endothelial cells exposed to antiphospholipid-antibody IgG had faster mean (+/- SE) plasma coagulation times than cells exposed to control IgG (trophoblasts, 8.7 +/- 2.0 vs. 21.3 +/- 2.9 minutes, P=0.02; endothelial cells, 9.8 +/- 0.8 vs. 14.2 +/- 1.2 minutes, P=0.04). CONCLUSIONS: Antiphospholipid antibodies reduce the levels of annexin V and accelerate the coagulation of plasma on cultured trophoblasts and endothelial cells. The reduction of annexin V levels on vascular cells may be an important mechanism of thrombosis and pregnancy loss in the antiphospholipid-antibody syndrome.

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Metadata

Authors
Rand, J. H., Wu, X.-X., Andree, H. A. M., Lockwood, C. J., Guller, S., Scher, J., & Harpel, P. C.
Venue
New England Journal of Medicine
Published
1997-07-17
Volume
337
Issue
3
Pages
154-160
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2316710385
Cited by
526
References
0
FWCI
24.73
Type
journal article
Language
en
Open access
bronze

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Rand, J. H., Wu, X.-X., Andree, H. A. M., Lockwood, C. J., Guller, S., Scher, J., & Harpel, P. C. (1997). Pregnancy Loss in the Antiphospholipid-Antibody Syndrome — A Possible Thrombogenic Mechanism. New England Journal of Medicine. https://doi.org/10.1056/nejm199707173370303

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