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find Keyword "色素性视网膜炎/治疗" 2 results
  • 腺相关病毒载体在视网膜色素变性基因治疗中的应用研究进展

    基因治疗是视网膜色素变性(RP)治疗研究的热点之一。经动物实验及临床试验证实, 腺相关病毒(AAV)载体因其无致病性、宿主范围广、转染和表达效率高、目的基因长期表达等优点成为视网膜疾病基因治疗的重要载体。但如何建立安全有效的基因治疗导入系统是目前临床需要首要解决的问题。此外, 由于基因的导向性和表达的调控性较为局限, 也限制了AAV载体介导的基因治疗在临床的广泛应用。进一步深入研究AAV的病毒生物学基础, 设计更多的组织特异性启动子以提高AAV载体的转染效率、靶向能力和安全性将为RP基因治疗带来新的曙光。

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  • Advances of optogenetics in the treatment of retinitis pigmentosa

    Retinitis pigmentosa (RP) is a disease that seriously affects vision. It mainly affects rod cells and causes night blindness. At the end of the disease, due to the simultaneous involvement of cone cells, the patient’s central vision and peripheral vision loss are not effective. There is no effective treatment method. However, some studies have found that although the function of photoreceptors is lost in the pathological process of RP, the function of bipolar cells and ganglion cells and the neural connection with the visual center are preserved, which provides a condition of therapeutic application in optogenetics for optogenetics. Optogenetics controls the excitability of neurons by expressing the light-sensitive protein represented by rhodopsin ion channel protein-2 on neurons, and has shown great application prospects in reshaping the photoreceptor function of the retina. The treatment of a type of retinal degenerative disease provides an effective treatment option.

    Release date:2018-11-16 03:02 Export PDF Favorites Scan
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