| Literature DB >> 18337603 |
Vera Eremina1, J Ashley Jefferson, Jolanta Kowalewska, Howard Hochster, Mark Haas, Joseph Weisstuch, Catherine Richardson, Jeffrey B Kopp, M Golam Kabir, Peter H Backx, Hans-Peter Gerber, Napoleone Ferrara, Laura Barisoni, Charles E Alpers, Susan E Quaggin.
Abstract
The glomerular microvasculature is particularly susceptible to injury in thrombotic microangiopathy, but the mechanisms by which this occurs are unclear. We report the cases of six patients who were treated with bevacizumab, a humanized monoclonal antibody against vascular endothelial growth factor (VEGF), in whom glomerular disease characteristic of thrombotic microangiopathy developed. To show that local reduction of VEGF within the kidney is sufficient to trigger the pathogenesis of thrombotic microangiopathy, we used conditional gene targeting to delete VEGF from renal podocytes in adult mice; this resulted in a profound thrombotic glomerular injury. These observations provide evidence that glomerular injury in patients who are treated with bevacizumab is probably due to direct targeting of VEGF by antiangiogenic therapy. Copyright 2008 Massachusetts Medical Society.Entities:
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Year: 2008 PMID: 18337603 PMCID: PMC3030578 DOI: 10.1056/NEJMoa0707330
Source DB: PubMed Journal: N Engl J Med ISSN: 0028-4793 Impact factor: 91.245