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基因疗法治疗遗传性眼病效果显著

新华网华盛顿2月8日电(记者任海军)美国研究人员8日在《科学·转化医学》杂志上报告说,3名遗传性眼病患者接受基因疗法治疗后,视力显著提高且无排异反应等不良情况发生。这为利用基因疗法治疗其他视网膜病变带来了希望。

  这3名患者患有罕见眼疾——莱贝尔先天黑内障。这种病通常在患者年幼时发作,患者视网膜细胞的一种基因发生变异,致使视力严重下降、眼球活动异常。到二三十岁时,患者可能完全失明。宾夕法尼亚大学和费城儿童医院研究人员利用腺病毒载体将修正基因RPE65植入患者眼球内,病毒将感染视网膜患病细胞,将变异基因“重写”为正常基因。

  出于谨慎,研究人员最初仅为每名患者视力较差的一只眼进行了治疗,经过几年的观察确认安全性和有效性后,研究人员又利用同样方法对患者另一只眼进行了治疗。治疗后患者能辨认出人脸,而这是接受治疗前做不到的,并且患者对弱光的敏感度显著提高。
本帖最后由 凤凰涅盘 于 2012-2-9 12:23 编辑

好消息,真令人振奋,今年开年就好消息不断

Second Eyes Treated Successfully in LCA Gene Therapy Clinical Trial at Children’s Hospital of Philadelphia
Drs. Albert Maguire, Katherine High and
Jean Bennett of CHOP
Feb. 8, 2012 – Clinical development of gene therapy for retinal degenerations has taken a big step forward, based on six-month results for three adults whose second eyes were treated in the Foundation-supported Phase I/II trial for people with Leber congenital amaurosis (LCA) at The Children’s Hospital of Philadelphia (CHOP). All three demonstrated improvement in visual and retinal function in their second eyes after treatment, which was administered one-and-a-half to three-and-a-half years after their first eyes were treated. The participants experienced further reductions in nystagmus, the involuntary eye movements common in people with LCA. And re-administration of the gene therapy was safe; no harmful immune reactions were observed.
The results were announced by CHOP today, and also reported in the February 8, 2012, online edition of Science Translational Medicine.  
“This is an important advancement for the retinal gene therapy field,” says Dr. Stephen Rose, chief research officer, Foundation Fighting Blindness. “It was critical to verify that a second exposure to the therapy’s viral delivery technology didn’t elicit an immune response that could jeopardize the treatment’s safety and effectiveness. And until now, there was no track record for administration of a second dose in people. Dr. Jean Bennett and her team at CHOP did a great job establishing confidence for re-administration in humans after completing two important large-animal studies of second-eye treatment.”
Dr. Bennett, who co-leads the trial with Dr. Albert Maguire, says, “We are delighted to be able to safely and effectively treat both eyes of our patients. But as you can imagine, they are even more delighted. Though these individuals have advanced retinal degeneration, we saw reported improvements in light sensitivity, visual acuity and visual fields in their newly treated eyes. Two of the subjects can now navigate in dimly lit settings. That’s very meaningful for them. Of course, long-term follow-up in these and additional subjects in our study will be important to understand the full safety profile, but we are very excited about these initial results.”
Dr. Bennett added that the improvements in vision enabled the participants to do activities they couldn’t do before, including walking around at night, shopping for groceries and recognizing faces.
After treatment of the second eyes, Dr. Manzar Ashtari used functional magnetic resonance imaging (fMRI) to observe activity in each participant’s visual cortex, the part of the brain used for vision. As expected, activity in the region of the brain that processes input from the second treated eye improved. But, remarkably, brain activity for the region corresponding to the initially treated eye also improved.
“We’ve known that our eyes in many ways work together, but this imaging study brings our understanding to a whole new level,” says Dr. Rose. “And it shows how beneficial it can be to treat both eyes.”
Twelve people with LCA caused by mutations in the gene RPE65, including a boy who was 8 years old when treated, are enrolled in the CHOP study, which began in late 2007. The participants, all of whom were virtually blind, demonstrated sustained vision improvement of varying levels after the initial treatment.
Dr. Bennett says that the compelling safety and efficacy data from these first three adult subjects has allowed the team to obtain the necessary regulatory approvals to invite the other study participants to undergo therapy re-administration to the second eye. Dr. Katherine High, the director of the Center for Cellular and Molecular Therapeutics at CHOP, continues to manage the critical regulatory aspects of these groundbreaking studies.
In addition to the CHOP study, Phase I/II clinical trials for LCA (RPE65 mutations) gene therapy are underway at: the Universities of Pennsylvania and Florida, Moorfields Eye Hospital in London, Oregon Health & Science University in Portland, and Hadassah Medical Organization in Jerusalem.
生命不息,战斗不止。
消息太振奋人心!谢谢飞弧分享。希望我的基因检测结果早日出来,也希望我国基因医疗早日临床!
今年的好消息真多啊,厚积薄发吧,干细胞和基因治疗
希望2012年使我们幸运的一年!谢谢大哥带来的好消息!
RPE65不是早就可以治疗了吗,希望更多的基因能够得到治疗!
希望明天会更好!
这个就是莱波士黑蒙的基因治疗
谢谢飞狐带来了好消息!是不是2008年进行实验的先天性黒矇基因治疗的后续报道?
8# 山重水复

是那时治疗了一只眼睛,现在又治疗了另外一只眼睛。
这么说基因治疗要比干细胞治疗快是吗
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