He cannot heal his father. But a scientist’s research can help everyone


When Sharif Tabebordbar was born in 1986, his father, Jafar, was 32 years old and already had symptoms of muscle atrophy. The mysterious illness would come to define Sharif’s life.

Jafar Tabebordbar could walk when he was in his thirties, but stumbled and often lost his balance. Then he lost his ability to drive. When he was 50, he could use his hands. Now he has to support one hand with the other.

No one could answer the question plaguing Sharif and his younger brother, Shayan: What was this disease? And would they develop it like their father did?

Growing up and seeing his father gradually decline, Sharif vowed to solve the mystery and find a cure. His quest led him to a doctorate in developmental and regenerative biology, the most competitive ranks in academic medical research, and a discovery, published in September in the journal Cell, which could transform gene therapy – a drug that corrects genetic defects – for almost any muscle wasting disease. This includes muscular dystrophies that affect approximately 100,000 people in the United States, according to the Muscular Dystrophy Association.

In an undated image provided via Sharif Tabebordbar, Sharif Tabebordbar, left, with his father, Jafar, mother, Tahereh Fallah, and brother, Shayan, on his graduation day from Harvard in 2016 (via Sharif Tabebordbar via The New York Times)

Scientists often use a deactivated virus called adeno-associated virus, or AAV, to deliver gene therapy to cells. But damaged muscle cells like those plaguing Sharif Tabebordbar’s father are difficult to treat. Forty percent of the body is made up of muscles. To transmit the virus to these muscle cells, researchers have to administer huge doses of drugs. Most viruses end up in the liver, damaging it and sometimes killing patients. The trials have been halted, the researchers are blocked.

Tabebordbar has managed to develop viruses that go directly to the muscles – very few end up in the liver. Its discovery could allow treatment with a fraction of the dose, and without the crippling side effects.

Dr Jeffrey Chamberlain, who studies therapies for muscle disease at the University of Washington and is not involved in Tabebordbar’s research, said the new method “could be taken to the next level,” adding that the same method could also allow researchers to precisely target almost any tissue, including brain cells, which is only beginning to be seen as gene therapy targets.

And Dr Francis Collins, director of the National Institutes of Health, which helped fund the research, said in a blog post that he held “potential to target other organs,” “thus potentially providing treatment for a wide range of genetic diseases. “

Tabebordbar’s small office at the Broad Institute at MIT and Harvard has a glass door that opens directly onto his bench. It’s not intimate. There are no photos, no books, no papers strewn on the white counter that serves as a desk. Even the whiteboard is clean. There, fueled by caffeine, he typically works 14 hours a day, except on days he plays soccer with a group at MIT.

“He’s incredibly productive and incredibly efficient,” said Amy Wagers, who held a PhD from Tabebordbar. Advisor and is Professor and Co-Chair of the Department of Stem Cells and Regenerative Biology at Harvard. “He works all the time and has this incredible passion and incredible dedication. And it’s contagious. It spreads to everyone around it. That’s a real skill – his ability to take a bigger picture and communicate it. “

Tabebordbar and his wife live in Cambridge, Massachusetts. He enjoys cooking Persian dishes and hosts a feast in his tiny apartment every Thanksgiving for a dozen friends. While working on his bench, he listens to Persian music, podcasts or audiobooks. He loves biographies and mentioned a passage he found significant in an autobiography of one of his heroes, England footballer Michael Owen.

Owen writes that when he learned he had been voted European Football Player of the Year in Europe, his reaction was moderate. “All I wanted was to score the next goal, the next hat trick and lift the next trophy,” Owen wrote. “Looking back, I was relentless in this regard and I have no doubt that this mindset was the key to my success.”

“It’s like me,” Tabebordbar said. “It’s amazing that we achieved this goal, but now” – he snaps his fingers – “we have to get down to business.

At the University of Tehran, he majored in biotechnology. After 4 and a half years, he obtained a master’s degree but started to apply for a doctorate. programs at top international universities researching muscular dystrophies, hoping it would lead to a discovery that might help her father. He ended up in Wagers’ lab at Harvard.

All the while, the question hung over him: what caused his father’s illness?

When his father came to Harvard to attend the 2016 graduation ceremony, Tabebordbar took the opportunity to have Jafar’s genes sequenced and uncovered the mystery. No mutation was found.

“How is it possible?” asked Tabebordbar.

Mouse tissues In an undated image provided by Sharif Tabebordbar, mouse tissue from Sharif Tabebordbar’s laboratory. From left to right: muscle injected with saline, muscle injected with AAV9 (used in ongoing clinical trials), and muscle injected with advanced AAV. Tissues injected with AAV carry a gene encoding a green fluorescent protein. (Sharif Tabebordbar via The New York Times)

More detailed and sophisticated testing ultimately revealed the answer: Her father suffers from an extraordinarily rare genetic condition, facioscapulohumeral muscular dystrophy, or FSHD, which affects about four to 10 in 100,000 people. It is not caused by a disease. mutation in a gene. Instead, it’s caused by a mutation in an area between genes, causing a toxic chemical to be excreted that kills muscle cells.

Much to Tabebordbar’s horror, he learned that he had a 50-50 chance of inheriting his father’s mutation. If he had it, he would contract the disease.

He was tested by a friend, who called him with the result.

Tabebordbar had inherited the mutation but, surprisingly, the mutated gene was missing the last piece of toxic DNA, preventing the onset of the disease.

“You are the luckiest of the unlucky guys,” he recalls telling his friend.

In Wagers’ lab, Tabebordbar worked on muscular dystrophy, using CRISPR, the gene editing technique. He attempted to use AAV to transport CRISPR enzymes to muscle cells where he could correct the mutation. As others have discovered before him, it was not that simple.

The Tabebordbar project at Harvard also suffered from the high dose issues. Although he was successful in correcting muscular dystrophy in mice – a feat reported at the same time by two other labs – it did not guarantee that gene therapy would work in humans. Different species – even different strains of mice – can have different responses to the same gene therapy. And the AAV doses were dangerously high.

After graduating from Harvard, Tabebordbar thought he had a chance to develop gene therapy for muscular dystrophy at a biotechnology company. But after about a year, the company called everyone into a conference room to tell them that there was going to be a reorganization and that the muscular dystrophy program was abandoned. Tabebordbar knew he had to go elsewhere.

He got a job in Pardis Sabeti’s lab at the Broad Institute and got to work. His plan was to mutate millions of viruses and isolate those that went almost exclusively to muscle.

The result was what he hoped for – viruses that focused on muscles, in mice and also in monkeys, making them much more likely to work in humans.

As scientists know, most experiments fail before anything succeeds and this work has barely begun.

“I will do 100 experiments and 95 will not work,” Tabebordbar said. But he said it is the personality that is required of a scientist. “The mindset I have is ‘this won’t work’. It makes you very patient.

He hopes his work will spare others the pain. However, the fate of his father weighs on him. Jafar Tabebordbar missed the window when it might still be possible to help him.

“He was born too early,” says his son.

This article originally appeared in The New York Times.

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