Vitaxin, a Humanized Monoclonal Antibody to the Vitronectin Receptor (α v β 3 ), Reduces Neointimal Hyperplasia and Total Vessel Area After Balloon Injury in Hypercholesterolemic Rabbits
| Autor: | Gregory A. Braden, Kimberly R. Coleman, David C. Sane, Mark C. Willingham |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Male
Neointima medicine.medical_specialty Intimal hyperplasia Smooth muscle cell migration Physiology Hypercholesterolemia Fluorescent Antibody Technique Apoptosis Pharmacology Antibodies Monoclonal Humanized Iliac Artery Cell Movement Transforming Growth Factor beta medicine Animals Humans Receptors Vitronectin Neointimal hyperplasia Hyperplasia biology business.industry Antibodies Monoclonal medicine.disease Surgery Cholesterol medicine.anatomical_structure Vitaxin Circulatory system biology.protein Vitronectin Rabbits Tunica Intima Cardiology and Cardiovascular Medicine business Angioplasty Balloon Blood vessel medicine.drug |
| Zdroj: | Circulation Research. 84:1268-1276 |
| ISSN: | 1524-4571 0009-7330 |
| Popis: | Abstract —The vitronectin receptor (α v β 3 ) mediates several biological processes that are critical to the formation of a neointima after coronary interventions. Blockade of α v β 3 could reduce neointima formation by inhibiting smooth muscle cell migration, decreasing transforming growth factor-β 1 expression, enhancing apoptosis, or reducing neovasculature. The effects of short-term administration of Vitaxin, a humanized monoclonal antibody to α v β 3 , on the responses to balloon injury were tested in hyperlipidemic rabbits. Balloon angioplasty was performed on the iliac arteries of male New Zealand White rabbits that were fed an atherogenic diet for 1 week before injury and until euthanization at 4 weeks. Rabbits were given either saline (control) or 1 of 2 dosing regimens of Vitaxin (high dose, 5.0 mg/kg, and low dose, 0.5 mg/kg), which were administered intra-arterially before injury and intramuscularly on days 2 and 3. High-dose and low-dose Vitaxin were equally effective in decreasing neointima formation even in the presence of hypercholesterolemia, a stimulus to α v β 3 expression. Vitaxin reduced transforming growth factor-β 1 and enhanced apoptosis in injured arteries. Despite these positive effects, Vitaxin administration was associated with a reduction in artery size, indicating a negative effect on remodeling. Vitaxin has a potential role in preventing intimal hyperplasia, especially if the negative effects on remodeling can be overcome, by dose adjustment or other strategies. |
| Databáze: | OpenAIRE |
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