Abstract
Widespread microvascular injury followed by vessel obstruction may lead to disseminated intravascular coagulation (DIC). We describe a murine model wherein leukocytes interacting with inflamed microvessels in vivo are activated by antibodies. Treatment of tumor necrosis factor alpha (TNF-alpha)-primed mice with anti-Ly-6G antibodies reproduced many of the features of septic or traumatic shock including microvessel obstruction and coagulation, severe vasculitis, respiratory difficulties, and vascular leakage. Mice lacking either E-selectin or P-selectin were protected from this reaction as were animals treated with a combination of either selectin-blocking antibodies and heparin or a selectin antagonist plus heparin. Combined blockade of leukocyte/platelet adhesion and coagulation may provide convincing protection in DIC.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies / administration & dosage
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Antibodies / pharmacology*
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Anticoagulants / administration & dosage
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Anticoagulants / pharmacology*
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Antigens, Ly / immunology
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Cell Adhesion / drug effects
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Disease Models, Animal
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Disseminated Intravascular Coagulation / drug therapy
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Disseminated Intravascular Coagulation / etiology
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Disseminated Intravascular Coagulation / prevention & control*
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Drug Therapy, Combination
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Heparin / administration & dosage
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Heparin / pharmacology
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Leukocytes / cytology
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Leukocytes / drug effects
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Leukocytes / immunology
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Mice
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Mice, Knockout
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Microcirculation / pathology
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Selectins / genetics
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Selectins / immunology*
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Survival Rate
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Tumor Necrosis Factor-alpha / administration & dosage
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Tumor Necrosis Factor-alpha / adverse effects
Substances
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Antibodies
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Anticoagulants
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Antigens, Ly
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Selectins
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Tumor Necrosis Factor-alpha
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Heparin