首页> 外国专利> RECOMBINANT ADENOVIRUS EXPRESSING αA-CRYSTALLIN GENE AND GENE THERAPY FOR RETINAL VASCULAR DISEASE USING SAME

RECOMBINANT ADENOVIRUS EXPRESSING αA-CRYSTALLIN GENE AND GENE THERAPY FOR RETINAL VASCULAR DISEASE USING SAME

机译:表达αA-克里斯塔林基因的重组腺病毒与基因治疗视网膜血管疾病的相同方法。

摘要

The present invention relates to recombinant adenovirus expressing αA-crystallin gene and to a gene therapy for retinal vascular disease using the recombinant adenovirus. The gene therapy using the recombinant adenovirus including αA-crystallin gene according to the present invention increases the expression level of αA-crystallin gene in injured of retinal pericytes to inhibit apoptosis and loss of pericytes, retinal vascular leakage, and leukocyte adherence in peripheral retinal vessels so as to protect pericytes. Therefore, the gene therapy using the recombinant adenovirus including αA-crystallin gene according to the present invention may be valuably used in the prevention and treatment of various retinal vascular diseases such as diabetic retinopathy.
机译:本发明涉及表达αA-晶状体蛋白基因的重组腺病毒和使用该重组腺病毒的视网膜血管疾病的基因治疗。使用根据本发明的包含αA-晶状蛋白基因的重组腺病毒的基因疗法增加了在视网膜周细胞的损伤中的αA-晶状蛋白基因的表达水平,以抑制周细胞的凋亡和丧失,视网膜血管渗漏和周围视网膜血管中白细胞的粘附。以保护周细胞。因此,使用根据本发明的包括αA-晶状体蛋白基因的重组腺病毒的基因疗法可有效地用于预防和治疗诸如糖尿病性视网膜病的各种视网膜血管疾病。

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