Increased Plasma Thrombospondin-1 (TSP-1) Levels Are Associated with the TNFα-308A Allele in Children with Juvenile Dermatomyositis |
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Authors: | Jennica Lutz Kristin G. Huwiler Tamara Fedczyna Toula S. Lechman Susan Crawford T. Randell Kinsella Lauren M. Pachman |
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Affiliation: | Division of Immunology/Rheumatology, Children's Memorial Hospital, Department of Pediatrics, Northwestern University Medical School, The Children's Memorial Institute for Education and Research, Chicago, Illinois, 60614;Department of Medicine, University of Wisconsin, Madison, Wisconsin;Department of Pathology, Northwestern University Medical School, Chicago, Illinois, 60614;Department of Pediatrics, Northwestern University Medical School, Chicago, Illinois, 60614 |
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Abstract: | Vascular occlusion is more frequent in children with juvenile dermatomyositis (JDM) who have the TNFα-308A allele. One of the potent anti-angiogenic factors is thrombospondin-1 (TSP-1). This study investigated the association of the TNFα-308A allele with circulating levels of angiogenic mediators, TSP-1, and platelet factor 4 (PF4) using fresh, platelet-poor plasma (PPP). The TNFα-308A allele was characterized by PCR amplification and NcoI digestion. Concentrations of TSP-1 and PF4 in PPP from 31 JDM patients and 25 matched pediatric controls were determined by ELISA. The majority of the JDM children with the TNFα-308A allele (7/12) produced more TSP-1 than their TNFα-308G counterparts (P < 0.05), and their TSP-1 values were inversely related to those for PF4 (P < 0.0006). We conclude that the increased circulating concentrations of TSP-1 associated with the TNFα-308A allele suggest that this anti-angiogenic regulator may play a significant role in the augmented vascular occlusion observed in JDM children with this genetic marker. |
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Keywords: | thrombospondin-1 platelet factor 4 TNFα -308A vascular occlusion and juvenile dermatomyositis |
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