Medical

Teenager's "incurable" leukemia cured by new base editing gene therapy

Teenager's "incurable" leukemia cured by new base editing gene therapy
Alyssa was diagnosed with T cell leukemia in mid-2021, and after exhausting all current therapies was on her way to palliative care. Now, six months after the experimental treatment, she is still in full remission.
Alyssa was diagnosed with T cell leukemia in mid-2021, and after exhausting all current therapies was on her way to palliative care. Now, six months after the experimental treatment, she is still in full remission.
View 1 Image
Alyssa was diagnosed with T cell leukemia in mid-2021, and after exhausting all current therapies was on her way to palliative care. Now, six months after the experimental treatment, she is still in full remission.
1/1
Alyssa was diagnosed with T cell leukemia in mid-2021, and after exhausting all current therapies was on her way to palliative care. Now, six months after the experimental treatment, she is still in full remission.

A teenager in the UK has become the first person to be treated with a revolutionary new gene editing therapy. The patient's incurable leukemia was effectively cleared using "base-edited" immune T-cells from a donor.

"This is a great demonstration of how, with expert teams and infrastructure, we can link cutting-edge technologies in the lab with real results in the hospital for patients," explained Waseem Qasim, a University College London researcher working on the project. "It’s our most sophisticated cell engineering so far and paves the way for other new treatments and ultimately better futures for sick children."

The technology behind the innovative new treatment is barely five years old, with researchers originally describing the technique as "CRISPR 2.0." Unlike prior CRISPR gene editing techniques, which act essentially like cut-and-paste tools, base editing is much more targeted and precise.

Our human genome consists of 3 billion base pairs made up of chemical units referred to by the letters A, C, G and T. Base editing allows for single-letter edits in genes, without causing breaks in DNA. If prior iterations of CRISPR were like molecular scissors, base editing is like using a pencil and eraser - changing single letters in base pairs to alter specific cellular mechanisms.

“Base editors allow precise nucleotide substitutions in the DNA without having to break the DNA to force the cell machinery to repair it and in the process make mistakes, which is the main mechanism of CRISPR-Cas9," explained Alena Pance, a geneticist from the University of Hertfordshire. "This property of base editors and the advances to improve their accuracy means that the exact wanted changes can be made, leaving no trace on the DNA otherwise, reducing the potential of collateral effects."

In this new instance, base editing was utilized to create a novel treatment for a 13-year-old patient suffering T-cell acute lymphoblastic leukemia. This incurable form of cancer involves a patient's T cells not maturing effectively and disrupting other blood cells.

Over the last few years scientists have made extraordinary breakthroughs in gene therapies for cancer. Gene editing a patient's T cells to target specific cancers is not a particularly new technique. However, the challenge with T-cell acute lymphoblastic leukemia is that gene editing T cells to target other T cells tends to result in the modified cells destroying other modified T cells.

So the new base editing technology allowed researchers to add several novel modifications to T cells, which were supplied by a healthy donor. The base edits altered several key markers that identify the immune cells as T cells. This meant the edited cells were essentially invisible to other T cells.

Other base edits to the T cells removed markers that were unique to the donor, turning the cells into a "universal" treatment. Crucially, this means the treatment can become an off-the-shelf drug given to many patients, in contrast to the slow and expensive personalized nature of current T cell therapies.

Simon Waddington, a professor of gene therapy at University College London, said there has been some stunning success with prior gene therapies, but the onerous process of creating the treatments has limited its broad viability. Harvesting immune cells from a patient, genetically modifying those specific cells, and then transplanting them back in the patient is a slow and time-consuming process.

“In this study, a bank of cells was generated – a single bank of cells which could be used to treat many patients," said Waddington. "This enables scalability, commercial viability, and standardization of the medicinal product.”

The very first clinical trial testing this kind of base-edited T cell therapy is currently underway, and reports from the very first patient given the treatment are stunning, to say the least. The young patient had exhausted all conventional treatments and was on a path to palliative care before being enrolled in the trial.

Within a month of receiving the experimental therapy the patient, named Alyssa, was completely leukemia free. Now, six months later, Alyssa is still in complete remission.

The preliminary clinical trial is looking to enroll another 10 patients over the coming years but this leukemia treatment is just the tip of the iceberg for base editing technology. At least three other trials are already underway testing base editing to treat sickle-cell anemia, high cholesterol and a blood disorder called beta-thalassemia.

David Liu, one of the researchers who developed the base editing technique just a few short years ago, said these few therapeutic applications for the technology are only just the beginning of what base editing can achieve.

“The vast majority of known genetic diseases require precise target gene correction as opposed to gene disruption or deletion,” Liu explained recently at a gene editing conference. "[These emerging technologies] give us hope that one day we may no longer be so beholden to the misspellings in our DNA.”

Sources: University College London, GOSH

4 comments
4 comments
Gonflage
What very cheering news amongst all the other items of gloom and doom that one reads of daily.

I am very happy for this young lady and for the clever folks involved in her treatment and in the therapy.
Hopeful
Wonderful work by true heroes. Hopefully many patients can quickly access this treatment.
nick101
Excellent news! I'm happy that this girl has a new chance at life, and the most exciting part is the treatment could be replicated and turned into affordable medicine!
Gregg Eshelman
There are around 1,000 people with Fibrodysplasia ossificans progressiva who would be very interested in this technique if it can be made to halt the progression of their genetic disorder. Even if all that can be done is to stop it from getting worse so they can have surgeries to remove some of the bone growths their lives would be much improved. Even better would be to have the treatment available to be administered right after birth, when FOP is typically identified.