She passed away from leukaemia a few years ago.

她几死于白血病。

They took disease-fighting T-cells from their patients and modified them to specifically attack leukaemia cells.

他们使用从病人身上获取治病的T细胞，然后修改为专门对付白血病的细胞。

In October 2023 the Indian government approved a cut-price domestic CAR-T therapy for B-lymphomas and B-acute lymphoblastic leukaemia, where one or more lines of treatment have failed.

202310，印度政府批准了一种针对B淋巴瘤和B急性淋巴细胞白血病的廉价国产CAR-T疗法，这些疗法中的一种或多种疗法都失败了。

At the top of that list were five which had previously been linked to leukaemia, but were not thought to affect solid tumours.

高踞名单列的5种基因是人们过去认为与白血病有关的，没想到它们也会影响实体瘤。

Several CAR-T cell therapies licensed to treat leukaemia and lymphoma, for example, use T-cells engineered with CARs that can recognise a protein called CD19, which is found on the outside of those cancer cells.

例如，几种获准治疗白血病和淋巴瘤的CAR-T细胞疗法使用经过CAR改造的T细胞，这些T细胞可以识别一种名为CD19的蛋白质，这种蛋白质位于这些癌细胞的外部。

US researchers have for the first time used gene therapy to successfully fight a particularly aggressive type of leukaemia in adults.

美国研究者首次使用基因疗法成功治疗一种专门的承认侵袭性白血病。

My twin brother died of leukaemia two years ago.

我双胞胎哥哥两因白血病去世了。

She was diagnosed with HIV in 2013 and leukaemia in 2017.

她于 2013 被诊断出感染艾滋病病毒，2017 被诊断出患有白血病。

In the 1940s, aware that folic acid could have positive effects on some anaemia sufferers, American pathologist Sidney Farber tried administering it to child leukaemia patients.

20世纪40代， 了解到叶酸可能对某些贫血患者有积极效果，美国病理学家西德尼·法伯尝试将其用于儿童白血病患者。

This was the revelation of the seventh known individual to reach apparently permanent remission from HIV infection after a bone-marrow transplant to treat leukaemia.

这是已知的第七个通过骨髓移植治疗白血病而实现艾滋病毒感染永久缓解的个体。

Childhood leukaemia and obesity were also potential risks.

儿童白血病和肥胖症也是潜在的风险。

2015. In the UK, genome editing is used to treat two babies with leukaemia.

2015. 在英国，基因编辑被用于治疗两名患有白血病的婴儿。

These include making four DNA-letter changes to immune cells so that they are better able to attack leukaemia, as well as a product that works for the same diseases as Casgevy.

这些措施包括对免疫细胞进行四个 DNA 字母的改变， 以便它们能够更好地攻击白血病，以及开发一种与 Casgevy 相同的疾病适用的产品。

After 2003 Several countries halt their gene therapy clinical trials after two SCID patients taking part in a trial in France developed leukaemia.

2003后，多个国家在法国进行的基因疗法临床试验中，两名SCID患者发展成白血病后，暂停了他们的基因疗法临床试验。

This was the first step to finding a successful treatment for childhood leukaemia.

这是找到成功治疗儿童白血病方法的第一步。