Nature Communications:新型基因疗法在亨廷顿舞蹈症小鼠模型中产生功能性神经元

2020-03-14 Allan MedSci原创

专注于神经退行性疾病的基因治疗公司NeuExcell Therapeutics今日宣布,其研究性基因疗法在亨廷顿舞蹈症(HD)的动物模型中产生了新的功能性神经元。

专注于神经退行性疾病的基因治疗公司NeuExcell Therapeutics今日宣布,其研究性基因疗法在亨廷顿舞蹈症(HD)的动物模型中产生了新的功能性神经元。该结果近期发表在《自然通讯》(Nature Communications)之上,表明该基因疗法可改善HD小鼠模型的症状并延长其寿命,因此该疗法或可用于治疗中枢神经系统(CNS)疾病。

NeuExcell的创始人和首席科学官Gong Chen博士领导的研究团队开发了这款基于腺相关病毒(AAV)的基因疗法,与未治疗的小鼠相比,经基因疗法治疗的小鼠表现出运动技能和存活率的显著改善。

Gong Chen博士是美国宾州州立大学的前教授,现在是中国暨南大学的大脑修复中心负责人,他率先采用了这种基因疗法来进行神经再生,该方法将特定的神经转录因子传递至大脑或脊髓的目标部位,转录因子可以重新编程受损区域中已经存在的细胞,以产生功能性神经元并修复受损的脑组织。

 

原始出处:

https://www.firstwordpharma.com/node/1708137

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    2020-03-24 liye789132251
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topicName=亨廷顿)], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=395f25, createdName=爆笑小医, createdTime=Mon Mar 16 02:27:07 CST 2020, time=2020-03-16, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1047781, encodeId=8b17104e781b4, content=梅斯里提供了很多疾病的模型计算公式,赞一个!, beContent=null, objectType=article, channel=null, level=null, likeNumber=53, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=f0620, createdName=CHANGE, createdTime=Sat Mar 14 14:27:07 CST 2020, time=2020-03-14, status=1, ipAttribution=)]
    2020-05-11 liuli5079
  5. 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  6. 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    2020-03-14 CHANGE

    梅斯里提供了很多疾病的模型计算公式,赞一个!

    0

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NEJM:慢病毒基因治疗联合低剂量白消安治疗SCID-X1婴儿

由此可见,慢病毒载体基因治疗结合低暴露、靶向白消安调节对新诊断的SCID-X1婴儿具有低度急性毒性作用,在中位随访16个月期间,可出现转导细胞的多系列植入,功能性T细胞和B细胞的重建以及NK细胞计数正常化。

Astellas斥资30亿美元收购Audentes,将基因治疗作为核心重点

Astellas以30亿美元的价格收购了Audentes Therapeutics,从而进军基因疗法,为其罕见疾病管线增加了晚期候选药物。

诺华的脊髓性肌萎缩症基因治疗药物Zolgensma,临床试验中出现第二次死亡事件

诺华公司最近公布了其脊髓性肌萎缩症(SMA)实验性基因治疗药物Zolgensma的临时中期研究数据,该研究表示正在调查第二次试验死亡是否与治疗有关。

研究证实使用CRISPR进行子宫内编辑,可在出生前治疗致命的肺部疾病

Science Translational Medicine最新发表的文章显示,科学家使用CRISPR基因编辑实现子宫内编辑,阻断动物模型中肺病疾病的致命突变,该有害突变在婴儿出生后数小时内会引起死亡。该研究证明,子宫内编辑可能是一种在出生前治疗肺病的有前途的新方法。

有关KO血友病的药物问世:基因治疗药物Valrox有望上市

甲型血友病,也称凝血因子八(FVIII)缺乏症,以凝血因子VIII缺失或缺陷引起的遗传性疾病,目前缺少根本治疗手段。据美国疾病预防控制中心(CDC)的报道,在美国,每5,000例活产胎儿中就有1例胎儿患有该病,血友病患者总数约为20,000人。据全球血友病发病率的准确数据,估计全球有超过40万的血友病患者。重症甲型血友病患者经常会发生自发性且疼痛的肌肉或关节部位的出血,该人群约占甲型血友病患者总数

拓展阅读

Genes & Diseases:电子科大黄璐琳教授团队重构调控亨廷顿舞蹈症行为的基因表达网络

该研究进一步证明纹状体异常神经元信号转导在导致HD相关表型行为中的重要作用,并为HD的进一步药物治疗干预提供了丰富的信息。

公益活动:未来可期!针对这种疾病的创新思路,或将成为神经退行性疾病治疗的曙光

编者按:随着全球人口老龄化程度的加剧,与之相关的疾病负担正在日益受到社会的重视,其中神经退行性疾病是备受关注的重点之一。全球疾病负担研究显示,目前有超过10亿人受到神经退行性疾病的影响,每年有近700

Neurology: 亨廷顿病基因携带者中,精神和认知症状普遍存在

亨廷顿病基因携带者中,精神和认知症状普遍存在

氘代丁苯那嗪在中国申报上市治疗亨廷顿舞蹈症(HD)

Austedo(deutetrabenazine)氘代丁苯那嗪片

欧洲药品管理局授予罗氏RG6042为优先药物用于治疗亨廷顿舞蹈症

罗氏的RG6042是一款靶向编码HTT蛋白的mRNA的反义链的创新疗法。通过与编码HTT蛋白的mRNA结合,RG6042能够降低所有HTT蛋白转译的发生,因此无论编码HTT的基因变异出现在哪里,该药物都可以减少有毒性的mHTT的产生。RG6042很可能成为靶向该疾病潜在病因的第一个治疗药物。

FRONT NEUROSCI:罕见病日:新版CRISPR技术有望根治亨廷顿舞蹈症

基因编辑CRISPR/Cas9技术的新版本用以治疗亨廷顿舞蹈症(Huntington Disease),比早期研究中的版本更安全和更具体,此项研究结果发表在近期的《Frontiers in Neuroscience》杂志上。