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COMPOSITIONS AND METHODS FOR REDUCING SPLICEOPATHY AND TREATING RNA DOMINANCE DISORDERS

机译:减少抗乳化病和治疗RNA优势障碍的组合物和方法

摘要

The disclosure features compositions and methods for the treatment of disorders associated with improper ribonucleic acid (RNA) splicing, including disorders characterized by nuclear retention of RNA transcripts containing aberrantly expanded repeat regions that bind and sequester splicing factor proteins. Disclosed herein are interfering RNA constructs that suppress the expression of RNA transcripts containing expanded repeat regions, as well as viral vectors, such as adeno-associated viral vectors, encoding such interfering RNA molecules. For example, the disclosure features interfering RNA molecules, such as siRNA, miRNA, and shRNA constructs, that anneal to dystrophia myotonica protein kinase (DMPK) RNA transcripts and attenuate the expression of DMPK RNA containing expanded CUG trinucleotide repeats. Using the compositions and methods described herein, a patient having an RNA dominance disorder, such as a human patient having myotonic dystrophy, among other conditions described herein, may be administered an interfering RNA construct or vector containing the same so as to reduce the occurrence of spliceopathy in the patient, thereby treating an underlying etiology of the disease.
机译:本公开内容具有治疗与不正当的核糖核酸(RNA)剪接相关的疾病的组合物和方法,包括抑制含有含有异常膨胀的重复区域的RNA转录物的核保留的疾病,所述重复区域结合和沉淀剪接因子蛋白。本文公开了干扰抑制含有膨胀的重复区域的RNA转录物的表达的RNA构建体,以及病毒载体,例如腺相关病毒载体,编码这种干扰RNA分子。例如,本公开特征在于干扰RNA分子,例如siRNA,miRNA和ShRNA构建体,其退火到染源肌肌肌肌肌肌肌肌肌肌肌瘤转录酶(DMPK)RNA转录物,并衰减含有膨胀的突发蛋白酶的DMPK RNA的表达。使用本文所述的组合物和方法,具有RNA优势障碍的患者,例如具有肌肌营养不良的人患者,其中包括其他条件,可以施用干扰RNA构建体或含有相同的载体,以便减少发生的患者的脾疗法,从而治疗疾病的潜在病因。

著录项

  • 公开/公告号EP3793566A1

    专利类型

  • 公开/公告日2021-03-24

    原文格式PDF

  • 申请/专利权人 UNIVERSITY OF WASHINGTON;

    申请/专利号EP20190803882

  • 发明设计人 CHAMBERLAIN JOEL;

    申请日2019-05-15

  • 分类号A61K31/7105;A61K48;A61P21;C12N15/113;C12N15/63;C12N15/85;C12N15/86;

  • 国家 EP

  • 入库时间 2022-08-24 17:53:00

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