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AIDS may be one of the most undesirable ...

    AIDS may be one of the most undesirable diseases in the world. Luckily, there is now hope for AIDS patients.

According to a recent paper published in the New England Journal of Medicine, Chinese scientists have successfully used CRISPR technology - a method of gene editing - to treat a patient with HIV. While it may not have cured the patient fully, it still represents a huge step forward in fighting the disease.

The patient was a 27-year-old Chinese man who was diagnosed with both AIDS and acute lymphoblastic leukemia (急性淋巴细胞白血病), a type of blood cancer. Despite his hopeless situation, doctors offered him a glimmer of hope: a bone marrow (骨髓) transplant to treat his cancer and an experimental treatment for his HIV.

They used this opportunity to edit the DNA in bone marrow stem cells from a donor before transplanting the cells into the patient.

Specifically, the treatment involved using the gene-editing tool CRISPR-Cas9 to delete a gene known as CCR5, which encodes a protein that HIV uses to get inside human cells. Without the gene, HIV is unable to infiltrate cells.

Talking about the gene, lead scientist Deng Hongkui told CNN, “After being edited, the cells - and the blood cells they produce - have the ability to resist HIV infection.”

Nineteen months after the treatment, the patient’s leukemia was in complete remission (缓解) and donor cells without CCR5 remained, according to the research paper.

Though the transplant did not cure the man’s HIV, it still showed the effectiveness of gene-editing technology, as there was no indication of any unintended genetic alterations - a major concern with past gene therapy experiments.

Amesh Adalja, a senior scholar at the Johns Hopkins Centre for Health Security in the United States, who was not involved in the study, praised the treatment.

“They did a very innovative experiment. It was safe,” he told Live Science. “It should be viewed as a success.”

Deng believes gene-editing technology could “bring a new dawn” to blood-related diseases such as AIDS and sickle cell anemia (镰刀形细胞性贫血).

“Thanks to this new technology, the goal of a functional cure for AIDS is getting closer and closer,” he said.

1.The technology of CRISPR is to ___________.

A.transplant cells B.encode genes

C.remove proteins D.produce cells

2.What was the result of the treatment?

A.CCR5 and other genes in the patient’s cells were changed.

B.The number of cells infected by HIV decreased.

C.Some of the patient’s blood cells could resist HIV infection.

D.HIV no longer existed in the patient’s cells.

3.What do we know about the experiment?

A.It provided an innovative way to cure AIDS patients.

B.It pointed out the problems of gene therapy.

C.It could offer a safe treatment for blood-related diseases.

D.It’s the first experiment to use gene-editing technology to treat AIDS.

 

1.B 2.C 3.C 【解析】 本文为说明文 。世界上最难治疗的疾病之一艾滋病现在有了新希望了,通过改变基因编码的方式,给治疗艾滋病4带来了曙光。 1.细节理解题。根据第二段中的“Chinese scientists have successfully used CRISPR technology - a method of gene editing - to treat a patient with HIV.” (中国科学家已经成功地利用CRISPR技术——一种基因编辑的方法——来治疗HIV患者。)可知,CRISPR技术就是用 一种基因编辑的方法。分析选项A. transplant cells移植细胞;B. encode genes编码基因;C. remove proteins去除蛋白质;D. produce cells产生细胞可知,B项与 题意相符,故选B。 2.细节理解题。文章第六段中的“After being edited, the cells - and the blood cells they produce - have the ability to resist HIV infection” (经过编辑,这些细胞——以及它们产生的血细胞——有能力抵抗HIV感染。)可知,病人的一些血细胞可以抵抗艾滋病毒感染。分析选项可知C项符合题意,故选C。 3.推理判断题。本题根据第 9段Amesh Adalja “They did a very innovative experiment. It was safe,” Amesh Adalja(他们做了一个有非常创新的实验。它是安全的。)倒数后两段Deng believes gene-editing technology could “bring a new dawn” to blood-related diseases such as AIDS and sickle cell anemia, “Thanks to this new technology, the goal of a functional cure for AIDS is getting closer and closer,” (邓认为,基因编辑技术可以为艾滋病、镰状细胞性贫血等血液相关疾病“带来新的曙光”。有了这项新技术,功能性治疗艾滋病的目标就越来越接近了。)可知 ,这个实验可以为血液相关疾病提供一种安全的治疗方法。故选C。
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