Suppression of Development of Ankylosing Spondylitis Through Soluble Flt-1
Author(s) -
Zhongxiang Yu,
Yuting Zhang,
Ningyang Gao,
Yong Kuang
Publication year - 2015
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000438571
Subject(s) - ankylosing spondylitis , vascular endothelial growth factor , medicine , arthritis , immunology , tumor necrosis factor alpha , monocyte , cancer research , macrophage , vascular permeability , biology , vegf receptors , in vitro , biochemistry
Circulating monocytes/macrophages are origins of osteoclasts that mediate the development of ankylosing spondylitis (AS). Moreover, infiltrated macrophages facilitate the AS progression through production and secretion of pro-inflammatory cytokines. Thus, suppression of the recruitment of circulating monocytes/macrophages may be an effective AS treatment, which is, however, not available so far in clinic. Soluble fms-like tyrosine kinase-1 (sFlt-1) is a decoy receptor for vascular endothelial growth factor (VEGF) to compete with VEGF receptor (VEGFR2) for VEGF binding in endothelial cells, while its application in treating AS and effects on the recruitment of circulating monocytes/macrophages has not been reported before.
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