Blocking Hemopexin With Specific Antibodies: A New Strategy for Treating Diabetic Retinopathy

糖尿病性视网膜病变 血-视网膜屏障 视网膜 医学 血红素 视网膜 血管通透性 视网膜病变 新生血管 内分泌学 埃文斯蓝 血管内皮生长因子A 血管内皮生长因子 血管生成 内科学 糖尿病 眼科 生物 生物化学 血红素 神经科学 血管内皮生长因子受体
作者
Patricia Bogdanov,Anna Duarri,D. Martínez,Anna Salas,Helena Isla-Magrané,Hugo Ramos,José Abellán Huerta,Marta Valeri,José García‐Arumí,Rafael Simó,Cristina Hernández
出处
期刊:Diabetes [American Diabetes Association]
卷期号:72 (12): 1841-1852
标识
DOI:10.2337/db23-0027
摘要

Hemopexin (HPX) is overexpressed in the retina of patients with diabetes and induces the breakdown of the blood-retinal barrier in vitro. The aim of this study was to evaluate whether HPX blockade by specific antibodies (aHPX) could avoid vascular leakage in vivo and microvascular angiogenesis in vitro and ex vivo. For this purpose, the effect of intravitreal (IVT) injections of aHPX on vascular leakage was evaluated in db/db mice and rats with streptozotocin-induced diabetes using the Evans Blue method. Retinal neurodegeneration and inflammation were also evaluated. The antiangiogenic effect of aHPX on human retinal endothelial cells (HRECs) was tested by scratch wound healing and tube formation using standardized methods, as well as by choroidal sprouting assays from retinal explants obtained in rats. We found that IVT injection of aHPX significantly reduced vascular leakage, retinal neurodegeneration, and inflammation. In addition, treatment with aHPX significantly reduced HREC migration and tube formation induced by high glucose concentration and suppressed choroidal sprouting even after vascular endothelial growth factor stimulation, with this effect being higher than obtained with bevacizumab. The antipermeability and antiangiogenic effects of IVT injection of aHPX suggest the blockade or inhibition of HPX as a new strategy for the treatment of advanced stages of diabetic retinopathy.Hemopexin (HPX) is the best-characterized permeability factor in steroid-sensitive nephrotic syndrome. We have previously reported that HPX is overexpressed in the retina of patients with diabetes and induces the breakdown of the blood-retinal barrier in vitro. Here, we report that intravitreal injection of anti-HPX antibodies significantly reduces vascular leakage, retinal neurodegeneration, and inflammation in diabetic murine models and that the immunoneutralization of HPX exerts a significant antiangiogenic effect in vitro and in retinal explants. The blockade of HPX can be considered as a new therapy for advanced stages of diabetic retinopathy.
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