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标题: FDA胚胎干细胞治疗AMD成功 [打印本页]

作者: baijianzhong    时间: 2011-7-15 14:24     标题: FDA胚胎干细胞治疗AMD成功

New Human Embryonic Stem Cell Study For Dry AMD And Stargardt's Macular Dystrophy

      Two patients have been treated using RPE (retinal pigment epithelial) cells derived from hESCs (human embryonic stem cells) in two Phase 1/2 clinical trials for dry age-related macular degeneration and Stargardt's macular dystrophy, Advanced Cell Technology Inc. has announced.

According to Dr. Steven Schwartz and Dr. Robert Lanza, the transplantation surgeries, which took place at the Jules Stein Eye Institute, California, were successful and both patients are recovering well.

Advanced Cell Technology says the two trials will enroll 12 patients in each one, with 3-patient cohorts in ascending dosage format. The primary endpoint is to establish safety and tolerability of hESC-derived RPE cells, after transplantation sub-retinally into patients with dry AMD and Stargardt's at 12 months. The investigators will also be looking for signs that the cells helped restore vision. In animal studies, rats experienced some recovery of vision.

Gary Rabin, interim chairman and chief executive officer of Advanced Cell Technology, said:


"This first treatment milestone is welcomed by scientists, stem cell advocates and patients hoping for cures. The two trials could not have started any smoother, and we are very pleased to announce that the procedures went well. The dosing of the first patients represents an important milestone for ACT and opens the doors to a potentially significant new therapeutic approach to treating the many forms of macular degeneration. We believe that these procedures represent a key step forward in therapeutic stem cell research, and the capacity to treat a variety of devastating diseases."


The studies' main investigator, Dr. Schwartz, said:


"One patient in each clinical trial, the Stargardt's trial and the dry AMD trial, has undergone surgical transplantation of a relatively small dose (50,000 cells) of fully-differentiated retinal pigment epithelial (RPE) cells derived from human embryonic stem cells. Early indications are that the patients tolerated the surgical procedures well. The primary objective of these Phase 1/2 studies is to assess the safety and tolerability of these stem cell-derived transplants. We will be carefully monitoring our patients over the course of the trials. We are privileged to be collaborating with ACT and honored to be working with these pioneering patients."


Stargardt's macular dystrophy, dry AMD and other types of atrophy-related macular degeneration are generally impossible to treat. These common forms of blindness urgently need safe and effective therapies.

Dr. Lanza said:


"Today -13 years after the discovery of human embryonic stem cells - the great promise of these cells is finally being put to the test. The initiation of these two clinical trials marks an important turning point for the field. While we will continue writing research papers and carrying out more research, it's time to start moving these exciting new stem cell therapies out of the laboratory and into the clinic.


Tens of thousands of people continue to die every day from diseases that could potentially be treated using stem cells. In the meantime, we intend to accelerate our efforts to translate new embryonic stem cell (ES) and induced pluripotent stem (iPS) cell therapies into the clinic. It has taken years of extensive research to get to this point. Our research and preclinical studies have demonstrated the safety and effectiveness of such therapies.

We hope these cells may provide a treatment option not only for degenerative eye diseases, but for a wide spectrum of other debilitating conditions, ranging from diabetes to vascular and autoimmune diseases. Our team remains committed to moving the field of regenerative medicine forward from bench to bedside."


In November, 2010, the FDA (Food and Drug Administration) approved Advanced Cell Technology's application to test cells created from human embryonic stem cells on 12 volunteers. Between 50,000 and 200,000 retinal pigmented epithelial cells derived from human embryonic stem cells will be injected into the patients' eyes. Hopefully, the new cells will replace those destroyed by dry AMD and Stargardt's macular dystrophy.

Human embryonic stem cell research is very controversial. The scientific community mainly believe that it can lead to treatments and cures for many devastating diseases. However, embryos a few days old have to be destroyed to get these cells, which many people are against for ethical reasons. There is also concern about safety - some people say the approach has not been tested enough and should not yet be tried on human beings.

Embryos used in embryonic stem cell research are usually extras that have been created in in-vitro fertilization (IVF) clinics - several eggs are fertilized in a test tube, but only one is implanted into the woman.

Advanced Cell Technology's stock price has gone up 170% so far this year. The company is valued at $285 million. Market experts believe it could be worth many billions if these trials are successful. Macular degeneration affects approximately 10 million people in the USA.

Embryonic stem-cell research has not been a money-maker so far. Advanced Cell Technology accumulated losses of over $180 million since it started in the mid-1990s.
What are hESC-RPE Cells?
RPE (retinal pigment epitheliom) is an extremely thin, pigmented cell layer just below the retina. It nourishes the photoreceptors as well as carrying away waste products. Human embryonic stem cells can turn into (differentiate) into any type of cell, including RPE cells.
SMD, Dry AMD and Degenerative Diseases of the Retina
SMD (Stargardt's macular dystrophy), a common form of macular degeneration, causes progressive loss of vision. The disease usually starts when the patient is between 10 to 20 years old. Photoreceptor loss caused by degeneration in the pigmented layer of the retina (RPE cell layer) eventually leads to blindness.

Degenerative retinal diseases are one of the most common causes of untreatable blindness worldwide. Experts estimate that in the USA and Europe alone approximately 30 million people suffer from macular degeneration - a global market in excess of $25 billion. One in every ten individuals aged between 66 and 74 years is thought to have macular degeneration symptoms, most of them with dry AMD, which is untreatable. Three in every ten individuals aged between 75 and 85 are believed to be affected.

Written by Christian Nordqvist
Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today



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作者: 凤凰涅盘    时间: 2011-7-15 15:28

看不懂啊,哪位高手翻译一下
作者: 雪山飞狐    时间: 2011-7-15 15:46

这么快就有结果了,真的高兴,虽然不是RP,但也有青少年黄斑变性,谢谢楼主!
作者: 衰神附体    时间: 2011-7-15 15:47

新人类胚胎干细胞的研究Stargardt AMD和干燥的黄斑萎缩



两个病人所受到的待遇和利用网膜色素上皮(RPE)细胞来源于为人类胚胎干细胞在临床试验两相半干年龄相关性黄斑变性和Stargardt的黄斑萎缩,高级细胞技术公司已经宣布。



根据博士史蒂芬施瓦茨医生和罗伯特·患病的移植手术,朱尔斯·斯坦发生在眼科研究所,加利福尼亚州,是成功的,两个病人正在康复中。



先进细胞技术试验将招收说,这两名12名患者,在每一个提升剂量组3-patient格式。主要终末点是建立的安全性和耐受性hESC-derived RPE细胞,在移植后患者sub-retinally干AMD和Stargardt在12个月。研究人员也在寻找迹象表明这些细胞帮助恢复视力。在动物实验研究中,经历了一些恢复大鼠的目光。



加里·拉宾、临时董事长兼首席执行官先进细胞科技公司,说:





“这第一次疗程里程碑是科学家,欢迎干细胞提倡者和病人希望医。这两个实验不可能开始任何光滑的,而且我们都很高兴的宣布程序进行得很顺利。第一个病人的定量表示为一个重要的里程碑,打开了门行为对潜在重要的新的治疗方法来治疗多种黄斑变性。我们相信这些程序代表了关键的一步治疗,干细胞研究,可治疗多种毁灭性的疾病。”





研究的主要调查者,舒博士说:





“一个病人在每一个临床试验是一种反复试验的方法,Stargardt干AMD试验,经历了外科移植相对小剂量(50000细胞)的网膜色素上皮fully-differentiated(RPE)细胞来源于人类胚胎干细胞。早期的迹象表明患者能耐受此手术。这些阶段的主要目的是评估1/2研究的安全性和耐受性这些干细胞源性移植。我们将密切监视病人的过程中试验。我们非常荣幸成为联合行动和荣幸能使用这些开拓病人的情况。”





Stargardt黄斑萎缩、干燥的AMD和其他类型的atrophy-related黄斑变性通常是无法治疗。这些常见形式的失明急需安全、有效的治疗方案。



兰德博士说:





“今天-13年之后才发现人类胚胎干细胞-这些细胞的伟大应许终于受到考验。开始这两个临床试验标志着一个重要的转折的领域。我们会继续写作的研究论文和开展研究,它的时间去开始移动这些令人兴奋的新的干细胞疗法和出实验室的诊所。





成千上万的人们继续死每一天从疾病有可能利用干细胞治疗。与此同时,我们打算促进我们的努力将新的胚胎干细胞(ES)和诱导多功能干细胞(iPS)细胞治疗的诊所。它花了多年的广泛研究到这一点。我们的研究和临床研究都证明的安全性与有效性这样的治疗。



我们希望这些细胞可能提供一种治疗选择的眼睛疾病不仅为变质,但对于广泛的其他退行性条件,从糖尿病到血管和自身免疫性疾病。我们的团队仍然致力于移动再生医学领域的前锋从板凳上,床边。”





2010年11月,FDA(食品和药物管理局批准的先进细胞技术应用到测试单元由人类胚胎干细胞在12名志愿者。在50000年和200000年之间视网膜色素上皮细胞来源于人类胚胎干细胞将注入到病人的眼睛。希望,这些新细胞将取代那些被干燥的AMD和Stargardt黄斑萎缩。



人类胚胎干细胞的研究是很有争议的。科学界主要相信它会导致治疗和治愈许多毁灭性的疾病。然而,胚胎几天老必须被摧毁让这些细胞,使许多人都反对出于伦理方面的原因。也有关心安全——一些人说这个方法还没有经过测试足够还不是试穿了人类。



胚胎用于胚胎干细胞研究,通常是创造了额外的体外受精(IVF)-数卵受精诊所在试管中,但只有一个是植入女人。



先进细胞技术公司的股票价格上涨了170%,今年到目前为止。本公司是价值2.85亿美元。市场专家相信它可能值得许多数十亿,只要这些实验是成功的。黄斑变性影响大约有1000万人在美国。



胚胎干细胞研究的还没有一个money-maker如此遥远。先进细胞技术的累积损失超过1.8亿美元,因为它开始在1990年中期秒。

hESC-RPE细胞是什么?

视网膜色素epitheliom(RPE)是一种极薄的色素细胞层,仅低于视网膜上。更滋养了感光细胞以及带走废物。人类胚胎干细胞可以变成(分辨率)到任何类型的细胞,包括RPE细胞。

SMD、干燥AMD和视网膜的退行性疾病

SMD(Stargardt的黄斑萎缩),一个常见的黄斑变性,使视力逐渐流失。这种疾病通常开始在病人10到20岁之间。光感受器丧失引起的色素变性在层(RPE细胞层视网膜)最终导致失明。



视网膜变性疾病的一种最常见的原因。世界范围内无法治愈的失明据专家估计,仅在美国和欧洲大约有3000万人患黄斑变性——一个全球市场超过250亿美元。一个在每十个人在66和74年之间被认为有黄斑变性症状,其中大多数与干AMD公司,这是无法治愈的。三人在每十个人在75年和85年之间被认为是影响。



基督教Nordqvist写的

版权:今日医学

不可擅自复印的今日医学
作者: 衰神附体    时间: 2011-7-15 15:48


作者: yeziwinds    时间: 2011-7-15 16:10

现在只是时间问题,现在这么多消息都是国外的,很想听听国内的具体情况。
作者: 在路上    时间: 2011-7-15 16:24

谢谢分享
作者: 渴望光明1968    时间: 2011-7-15 17:12

好消息,谢谢楼主的分享,
希望这种治疗快点到来
作者: baijianzhong    时间: 2011-7-15 18:06

it's time to start moving these exciting new stem cell therapies out of the laboratory and into the clinic
   把胚胎干细胞治疗这项技术从实验室走出来并应用到临床的时候到了。
作者: 福娃晶晶    时间: 2011-7-15 18:09

9# baijianzhong


如果是“把胚胎干细胞治疗这项技术从实验室走出来并应用到RP临床的时候到了”,那就好了。不过应该很快了吧?
作者: xp1207    时间: 2011-7-15 19:08

6# yeziwinds


国内的医生也在等国外的消息,只有这样他们才可以开药,拿回扣,他们也只能干干这个了。。。。
作者: 南国乞儿    时间: 2011-7-15 19:33

谢谢楼主.希望这样的消息越多越好.
作者: 山重水复    时间: 2011-7-15 19:38

太高兴了!
谢谢楼主给我们带来了好消息。
作者: zhwei_313    时间: 2011-7-15 19:41

谢谢楼主,很好的消息!
作者: chinatiger    时间: 2011-7-15 20:23

绝对的好消息
作者: 重获光明    时间: 2011-7-15 21:56

谢谢楼主分享!
作者: rebecca911    时间: 2011-7-15 22:32

太好了。。。
作者: 我要看得见!    时间: 2011-7-15 23:24

谢谢楼主的分享




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