【亚博app】科学家将要用基因编辑技术治疗先天失明

发布者: 发布时间:2021-01-31
本文摘要:CRISPR is coming for your body. While that may sound like the tagline of a horror film, its potentially the future of medicine, as the gene-editing technique is about to be used for the first time inside the bodies of presumably willing patients.CRISPR(出簇规律间隔的短回文反复序列,近年来被指出是原核生物适应性免疫系统结构)将要转入你的身体。

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CRISPR is coming for your body. While that may sound like the tagline of a horror film, its potentially the future of medicine, as the gene-editing technique is about to be used for the first time inside the bodies of presumably willing patients.CRISPR(出簇规律间隔的短回文反复序列,近年来被指出是原核生物适应性免疫系统结构)将要转入你的身体。虽然这听得上去有可能类似于一部恐怖电影的口号,但这或许是医药研究的未来,因为基因编辑技术将首次被用作毕竟是强迫拒绝接受的病人的身体上。

The first trial could be an impressive feat of modern medicine: Scientists hope to use CRISPRs gene-editing magic to restore sight to people with an inherited form of blindness called Leber congenital amaurosis.这次尝试有可能是现代医药的一次令人印象深刻印象的伟业:科学家期望利用CRISPR基因编辑的魔力来完全恢复遗传性失聪(又被称作莱伯士先天性黑朦)的人的视力。Its the most common cause of inherited childhood blindness, occurring in about 2 to 3 of every 100,000 births, according to the AP.据美国牵头通讯社报导,这是儿童遗传性失聪最少见的原因,每十万个新生儿中就不会有2~3个人患上遗传性失聪。People with the disease lack just one gene, the gene that converts light into signals to the brain and lets the eyes do their job.患上这种疾病的人只缺乏一种基因,这种基因把光转化成信号并起源于大脑,然后使眼睛发挥作用。

The hope is that adding that gene through a one-time CRISPR treatment will cure them, permanently editing their DNA and letting them see.期望通过一次CRISPR化疗就可以植入这种基因,并医治这种疾病,使DNA被永久性编辑,让他们得见光明。This is undoubtedly a more noble use of CRISPR than making spicy tomatoes.相比生产辣味的西红柿,这毫无疑问是CRISPR技术的一项更加崇高的运用。Its a good trial for the cutting-edge—and controversial—technology, because theres already some solid proof that the disease is treatable on a genetic level.对于这项先进设备且有争议的技术而言,这是一次不俗的尝试,因为有数可信的证据指出这种疾病在基因层面上是可化疗的。

Thanks to a gene therapy called Luxturna, which is already on the market, scientists know that injecting a replacement gene into cells in the retina can cure the ailment .好在早已上市的Luxturna基因疗法,科学家了解到向视网膜中的细胞流经一种替代基因可以医治疾病。CRISPR would work by similarly delivering new genetic material to the eye, giving researchers the perfect testing ground for using the new medical procedure in humans, before turning to more complicated diseases like cancer.CRISPR某种程度通过把新的遗传物质植入眼睛来发挥作用,这在改向用其研究化疗癌症这种更加简单的疾病之前,为研究人员在人类身上用于这种新的医疗程序获取了极致的试验依据。Two companies, Editas Medicine and Allergan, will test the technique in up to 18 people at hospitals around the United States, starting this fall.在美国周围的医院里,艾迪塔斯医药公司与阿勒根两家公司将于今年秋天开始在多达18人身上测试这种技术。

The new study will test children at least 3 years old and adults with a range of vision.这项新的研究将在视力情况有所不同的三岁以上的儿童及成年人身上展开测试。


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