AAN:Magenta Therapeutics的干细胞疗法MGTA-456的2期临床数据喜人

2019-05-11 不详 MedSci原创

在宾夕法尼亚州费城的美国神经病学学会年会上,Magenta Therapeutics宣布其细胞疗法MGTA-456的2期临床数据。MGTA-456治疗肾上腺脑白质营养不良(cALD)患者后,进行了为期6个月的随访结果显示MRI稳定的神经功能评分和脑炎症的早期和持续消退。

在宾夕法尼亚州费城的美国神经病学学会年会上,Magenta Therapeutics宣布其细胞疗法MGTA-456的2期临床数据。MGTA-456治疗肾上腺脑白质营养不良(cALD)患者后,进行了为期6个月的随访结果显示MRI稳定的神经功能评分和脑炎症的早期和持续消退。

MGTA-456是一种细胞疗法,旨在提供与患者完美匹配的高剂量造血干细胞

在报告中,Magenta Therapeutics的Kevin Goncalves博士重点展示临床前数据,证明MGTA-456中的高剂量干细胞可加速并改善人小胶质细胞在移植小鼠大脑中的植入。

cALD是一种快速进展的疾病,进展迅速的患者通常具有较差的预后。MGTA-456治疗的两位患者的神经功能评分稳定,脑部炎症持续减少,表明该疾病的进展已被阻止。

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  5. 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  6. 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time=2019-05-13, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1350820, encodeId=2df31350820f5, content=<a href='/topic/show?id=a2fb1e385a1' target=_blank style='color:#2F92EE;'>#therapeutics#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=24, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=17385, encryptionId=a2fb1e385a1, topicName=therapeutics)], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=4c37265, createdName=zhaojie88, createdTime=Mon May 13 12:56:00 CST 2019, time=2019-05-13, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1446456, encodeId=45f61446456e0, content=<a href='/topic/show?id=2e3016e437' target=_blank style='color:#2F92EE;'>#AAN#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=41, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=1674, encryptionId=2e3016e437, topicName=AAN)], attachment=null, 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    2019-09-27 grace5700
  7. 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    2019-05-13 bluefate123
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    2019-05-12 坚强007

    向挑战病魔的科研人员致敬!

    0

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TiGenix NV和武田制药公司近日宣布,欧盟委员会(EC)已批准Alofisel(Darvadstrocel,前期名称为Cx601),用于治疗成人非活动性/轻度活动性克罗恩病患者的复杂肛周瘘,这些患者往往对至少一种常规疗法或生物疗法耐受。Darvadstrocel这次获得欧盟委员会的首肯标志着首个异体干细胞疗法在欧洲范围内取得了成功。

出生之前就能把病治了?这种干细胞疗法或许有效

6 月 20 日消息,据 Singularityhub 报道,在伊莱安娜·康斯坦丁诺(Elianna Constantino)出生之前,她就曾在母亲体内假死过。伊莱安娜患有罕见的遗传性血液疾病——地中海贫血病(alpha thalassemia major),它会阻止红细胞正常形成。这种疾病没有治愈方法,对发育中的胎儿通常是致命的。

干细胞疗法或可逆转帕金森症 日本开启全球首次人体实验

据外媒7月30日报道,日本近日启动世界首个利用干细胞治疗帕金森症的人体试验,此前的动物实验表明,这项研究能积极逆转该疾病。京都大学的研究小组于7月30日宣布了世界上首例利用干细胞治疗帕金森症的人体试验。研究人员计划将500万个诱导多能干细胞(iPS)注射到患有帕金森症的病人大脑中,来自健康捐赠者的iPS细胞将被发展成能够产生多巴胺的脑细胞,而这种脑细胞在帕金森氏症患者身上是无法生成的。帕金森氏病是

EASL大会:Promethera干细胞疗法HepaStem在2a临床显示出对急性肝衰竭治疗的安全有效性

比利时生物技术公司Promethera在维也纳EASL大会上展示了其干细胞疗法HepaStem,治疗急性慢性肝功能衰竭(ACLF)以及预防急性失代偿(AD)患发生ACLF的2a期试验结果。

视网膜修复

视网膜受损时,视力会受到很大的影响。不幸的是,虽然全球有数亿人患有视网膜变性,但目前还没有有效的治疗方法。然而,随着干细胞技术的不断进步,新方法有望修复视网膜。无论是通过培养新细胞,然后将它们移植到视网膜中,还是通过从头开始构建整个视网膜,干细胞疗法有望提高视网膜变性患者的视力,还他们一个清晰的世界。

悉尼大学研究显示原弹性蛋白将带来更低廉有效的干细胞疗法

干细胞对于修复和构建人体组织如皮肤和肌肉等至关重要。全世界对于干细胞的需求远远供不应求,因此研究人员一直在寻找更高效应用干细胞的方法。 荧光标记间充质干细胞在原弹性蛋白上生长 目前研究人员发现了一种利用原弹性蛋白廉价而快速地生成更多干细胞的方法。该研究发表于《美国科学院院报》,共同作者为悉尼大学查尔斯·珀金斯中心、生命与环境科学学院和博世研究所的Giselle Yeo博士和Anthony Wei