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r. David Williams very much hopes the White House’s $755 million “cancer moonshot” finds cures, that Sean Parker’s $250 million “Dream Team” brings effective immune-system treatments to every kind of tumor, and that the $370 million raised by Hollywood-based Stand Up to Cancer fuels discoveries that make malignancies as treatable as headaches.

All Williams wants is $5 million — a rounding error to the billionaires making nine-figure donations to cancer research — to run a clinical trial that has a good chance of curing sickle cell disease.

There is no moonshot for sickle cell. There are no “ice bucket challenges.” When fundraisers at Boston Children’s Hospital and Dana-Farber Cancer Institute, where Williams is president of the Cancer and Blood Disorders Center, ask donors to support sickle cell research, benefactors say they prefer to fund efforts that promise to help the adorable little kids stricken with cancer.

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There are many theories about why that is, and why the lack of urgency and even interest extends to scientists. Fewer than a dozen US labs are working all-out on sickle cell disease, a number that has stayed constant for years, said Dr. Stuart Orkin of Boston Children’s. “I’m not sure why there are so few,” he said. “Maybe [the biology of sickle cell disease] seemed too simple, or maybe it isn’t sexy enough.”

Or maybe the disease strikes the “wrong” people.

“Sickle cell patients have never been at the front of the line,” said Dr. David Nathan, 87, a past president of Dana-Farber who helped discover the only drug that partly treats it. “It strikes Italians, Greeks, blacks. … This work, especially clinical trials, is hugely expensive, and the National Institutes of Health and private foundations haven’t prioritized it.”

Virtually every scientist thinks the disease he or she studies is underfunded. What’s different about sickle cell is that scientists can point to specific turning points when a few more people at the lab bench would have made a significant difference to the pace of progress, and to specific studies now on the drawing board that could, with a concerted national effort, cure the disease.

“This is the right time for a sickle cell moonshot, a concerted effort to focus resources — not just financial resources but intellectual resources — on a goal,” said Williams. “The technology has advanced to the point where we can talk about curing this disease.”

In healthy people, blood cells are round and flexible. But in people with sickle cell disease, blood cells are deformed and cause a range of health problems. Hyacinth Empinado/STAT

‘I try not to think about it’

Every year about 300,000 babies around the world are born with sickle cell disease, the result of a mutation in the gene for hemoglobin, the oxygen-carrying molecule in red blood cells. Only infants who inherit the defective gene from both parents — an estimated 100,000 people in the United States — have it.

The mutation, discovered in 1956, causes red blood cells to cramp up into a crescent shape that makes them clump, impeding their flow through blood vessels. As a result, patients can suffer anemia, infections, fatal organ failure, tissue damage, strokes, and pain so intense it feels like a pickaxe-in-the-skull migraine everywhere in the body.

Camille Lonzer had her first such sickle cell crisis, as the severe pain is called, a year ago, when she was 13, the latest blow from a disease that for years had sent her to the hospital with fevers and infections seemingly as often as other little girls go to birthday parties.

Her parents, who work for pharmaceutical companies near Chicago, have been tireless in managing Camille’s sickle cell disease, including massaging her in an effort to keep her blood flowing and the pain at bay. So far, the disease has not kept Camille “from doing everything I want,” she said. But the arrival of the pain crises, she and her parents worry, might change that.

“I try not to think about it,” she said. “I try to imagine myself somewhere else.”

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Camille began taking the only Food and Drug Administration-approved sickle cell drug, hydroxyurea, after the pain crisis. Hydroxyurea is an old cancer medication whose effect on sickle cell was discovered serendipitously by Nathan and his colleagues at Boston Children’s. It can reduce episodes of sickle cell crisis, but helps only about half of patients, can cause serious side effects, and does nothing about the sickling itself. “We were hoping not to have to” put Camille on the drug, said her mother, Pamela Lonzer.

A bone marrow transplant can cure the disease, but most patients can’t find a match, the procedure has a fatality rate of up to 5 percent, and patients need to be on anti-rejection drugs forever.

While other discoveries of disease-causing mutations led to treatments and even cures in, for example, 26 years for cystic fibrosis or 16 years for HER2-positive breast cancer, the discovery of the sickle cell mutation has led to exactly zero after 60 years.

Not that there haven’t been opportunities.

Missed chances

Physicians have long been struck by how some people with the sickle cell mutation are mostly fine, with few or none of the disabling symptoms. In 1948 scientists guessed why: These patients, hematologists wrote in a paper on “the paucity of sickle cells in newborn Negro infants,” were still making a form of hemoglobin that the body ordinarily stops producing in the first year of life. If just 15 percent or so of the body’s hemoglobin is “fetal hemoglobin,” scientists learned later, it keeps the disease at bay.

Orkin, who had done pioneering research on thalassemia and other blood disorders as well as the genetics of normal blood cell development, was part of the team that in 1984 discovered that hydroxyurea somehow affects DNA so as to resume the production of fetal hemoglobin at levels more typical of infancy. He began searching for the genetic magic that accomplished that.

He and his colleagues got clues by studying Saudi Arabian patients who had the sickle cell mutation but only mild symptoms thanks to the fetal hemoglobin they kept making into adulthood. But the genetic basis of that is “complex and requires interaction with additional factors,” Orkin and his colleagues wrote in 1989.

It wasn’t a surrender, or a warning that the genetics of sickle cell were too tough to decipher. It was what, in many other fields, would be taken as a challenge, drawing hordes of young scientists to an intriguing puzzle.

That did not happen. By the late 1980s, scientists knew that genetic on-off switches — transcription factors — were important for the development of blood cells. “But no one had a clue which transcription factors regulated the switch from fetal to adult hemoglobin,” said Orkin, who is also chairman of pediatric oncology at Dana-Farber. By sheer bad luck, his and other labs that set out to identify those molecules looked in the wrong kinds of cells, cells that didn’t make the switch. With barely a dozen labs working on sickle cell, the field didn’t have the critical mass that might have led someone to figure out what kinds of cells to use in experiments seeking the fetal-to-adult switch.

They hit dead end after dead end, and with little incentive to keep hunting, “we went off and did other things,” said Orkin. “I like to do things that work, and sickle cell wasn’t working.”

He turned away from sickle cell research for about a decade, spending the 1990s on the genetics of normal blood cell development. He still thought about sickle cell disease, trying to imagine how the genetics of the fetal-to-adult hemoglobin switch worked. But no one was banging on his door to fund sickle cell experiments, no Hollywood charity dangled millions of dollars in grants in front of him.

In the early 2000s, Harvard medical student Vijay Sankaran, working in Orkin’s lab, said he wanted to study the fetal-to-adult hemoglobin switch. Orkin asked if Sankaran was sure; he worried that Sankaran’s budding career would tank as a result of searching fruitlessly for the molecular genetics of sickle cell. His caution seemed to be borne out when, for nearly three years, Sankaran’s experiments repeatedly failed. It turned out he was looking for the crucial transcription factor gene on the wrong chromosome.

An innovators’ maxim is to “fail fast,” so developers can quickly pivot from unproductive paths. If many scientists had been competing with Sankaran to find the gene, who knows if he would have abandoned his search on the X chromosome in weeks, not years. And who knows how much faster key discoveries would have been made.

Sankaran finally bagged his quarry in 2008, when he — with others in Orkin’s lab — identified the gene that turns on production of adult hemoglobin. Called BCL11A, it’s located on chromosome 2. When they suppressed BCL11A in human cells growing in lab dishes and in mice, they reported in Science in 2011, blood cells kept making fetal hemoglobin and the mice were cured of sickle cell. Around that time, Sankaran and his team discovered another gene that helps flip the switch, called MYB; suppressing it, too, increased production of fetal hemoglobin.

That opened the door to using gene therapy to cure sickle cell.

Our bodies switch from fetal blood to adult blood as we age. Here's how the blood we have at birth could help those with sickle cell disease. Hyacinth Empinado/STAT

‘We didn’t scream enough’

When David Williams was a newly minted physician 30 years ago, the Children’s Hospital hematology caseload was about evenly split between kids with hemophilia and kids in sickle cell crisis. Since then, treatments for hemophilia have become so successful that they’re practically cures, and children almost never show up with uncontrollable bleeding.

“So we see almost all sickle cell,” Williams said, explaining why he jumped at the chance to build on Orkin’s discoveries. “It’s really sad that’s the case.”

He began developing an experimental therapy based on the genetics of sickle cell, in particular the idea that knocking out only enough BCL11A to reactivate some fetal hemoglobin production should avert the devastating symptoms of the disease. Therapies that prevent BCL11A from flipping fetal hemoglobin to adult hemoglobin can therefore be far from perfect.

But Williams immediately hit the same speed bump that Orkin and Sankaran had: too few resources. He needed a way to slip genetic material into cells, using a harmless virus (viruses are great at infiltrating cells). It took his lab two long years to figure out how to do that safely, partly because “I had only one postdoc working on it,” he said. “With more people, it would have taken much less time.”

His plan is to pack molecules called antisense RNAs into lentiviruses, which are as efficient at delivering genetic material into cells as pizzerias are at delivering menus into apartment-house vestibules. The viruses would carry the RNA into blood stem cells isolated from a patient’s bone marrow. Antisense RNA basically hogties the messenger molecules that carry instructions from the BCL11A gene, triggering a sequence of events that cause some blood cells to make fetal hemoglobin. That should keep at least some fetal hemoglobin from being switched to the adult form.

“Most people think you’d have to correct only 10 to 20 percent of cells to cure somebody,” Orkin said. About 30 percent was enough to cure the mice in his 2011 Science study.

Gene therapy would likely be too expensive for use in India and the African countries where sickle cell is common, so Orkin hopes a drug could tie up BCL11A. “That’s where I think a moonshot really is needed,” he said: drawing clever, imaginative researchers to find molecules able to disable enough BCL11A to keep enough cells making fetal hemoglobin to cure the disease.

No one minimizes the long, hard slog that would take. The gap between biological discovery and disease treatment is so wide, it’s called the valley of death. Gene-activating molecules like BCL11A are often considered “undruggable,” meaning it’s very difficult to invent a compound that affects them. “But a moonshot would bring in structural biologists and chemists [and others] who could find a drug targeting BCL11A,” Orkin said.

“You need people to think about, can you get molecules to bind to [BCL11A]?” Orkin said. “Can you get molecules that degrade it? … Those are not easy tasks.”

The what-ifs — if 50, not 10, labs pursued sickle cell; if Orkin had been able to enlist more scientists in the 1990s transcription-factor hunt; if Williams had had the resources to support four or five postdocs looking for a safe vector — are impossible to answer. But “as a scientist and a physician, it’s one of my major frustrations,” said Williams, referring to how little support and attention sickle cell gets from scientists, funders, and the government. “This is a disease that devastates the families and the lives of the children.”

“Maybe it’s our fault,” said Nathan about the paucity of resources devoted to sickle cell over the decades. “Maybe we didn’t scream enough” for more funding, more bodies, more attention. “But it’s just not right” how little attention the disease gets.

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Pamela Lonzer seconds that. When Camille was born with sickle cell disease, “I thought my world was ending,” she said. Although Camille, whose favorite school subjects are science and writing, has participated in research on exercise and pain, the family is still waiting for a clinical trial of a drug or other therapy that might actually cure her.

“This is a disease that doesn’t get the attention or the funding it should,” Lonzer said. “There’s a stigma that comes from thinking it affects only African-Americans. People dismiss it by saying, ‘Oh, sickle cell patients just have pain.’”

Efforts to cure sickle cell (as well as to alleviate some of its symptoms without going all the way to a cure) are underway at pharmaceutical companies and biotechs. Novartis announced last year that it is collaborating with Intellia Therapeutics, which hopes to develop treatments by using CRISPR genome-editing technology to switch the gene for fetal hemoglobin back on.

That would probably be done by extracting progenitor blood cells from a patient, using CRISPR to increase production of fetal hemoglobin relative to adult hemoglobin, and then infusing fetal-hemoglobin-making cells back into the body. By targeting those progenitor cells, said Craig Mickanin of the Novartis Institutes for BioMedical Research, “you can repopulate the whole lineage.” But because only some cells have to make fetal hemoglobin, “we don’t feel we have to correct 100 percent of the cells.”

Sangamo BioSciences is using a different genome-editing technique, called zinc fingers, to treat blood stem cells outside the body. But instead of disrupting BCL11A directly, Sangamo aims to disable an earlier step in the BCL11A process that Orkin and his team discovered in 2013. Called an enhancer, it is less likely to affect immune cells where BCL11A also operates, averting the risk of dangerous side effects.

“Breaking the enhancer is more feasible than fixing the hemoglobin mutation,” said hematologist Dr. Daniel Bauer of Dana-Farber/Boston Children’s and a codiscoverer of the BCL11A enhancer. “I think we have a unique opportunity to cure sickle cell disease.”

The American Society of Hematology plans to call for a sickle cell moonshot this fall. Thanks to the discoveries about the genetics of hemoglobin and the development of genome-editing technology, “we really do have opportunities” to develop a cure, said ASH vice president Dr. Alexis Thompson of Children’s Hospital of Chicago. “But we have to go after it with passion and urgency. The time is now.”

ASH can do little more than make that plea to the public, elected officials, and the NIH, whose National Heart, Lung, and Blood Institute funds sickle cell research. But the institute also funds research on heart disease, which has a much larger constituency. “I am not holding my breath,” Orkin said.

Williams is slowly getting governmental and other approvals for the small clinical trial he’s planning. He thinks a moonshot — with all the coordination, resources, and publicity that could bring — might organize multiple medical centers to participate in both this trial and, if it succeeds, larger ones. He hopes to start recruiting patients (two children, two teenagers, and two adults) in September.

“This is absolutely going to work,” Williams said — if only someone would pony up $5 million.

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  • I have a child with sickle cell disease and for the first time, I’m reading about someone (Camille’s mother) who expressed exactly how I felt, when she said she felt as though her world was ending.

  • As a scientist by trade and a hip hop fan, reading this after a noted rapper passed after a lifetime of sickle cell anemia is striking. At least we know there are labs to target this issue, and possibilities of a way out.

  • I am in love with a young woman with sickle cell anemia. I want to help find a cure.I will pursue a way to raise awareness and a way to raise funds.I truly believe that modern medicine , scientists and the medical profession can and will succeed in finding a cure.I will give my life for her.

  • My husband is 37 yrs. His sickle cell anemia was dorment from the age 10-27. After his 27th bday he suffered a major crisis which caused him to be hospilized for 3mon sedated. 2 years after he began to have frequent crisis and needed his gall bladder removed. Following year he began to have severe constant chest pain. He also was diagnosed with testicular cancer and had surgery. The following year we developed AVN and was in need of a hip surgery. He had hip surgery for his right hip. He had a crisis the following afternoon which caused his right leg to become completely knumb and followed be nerve damage and a foot drop. This year alone he has been hospitalized 90% of the year. We have been doing research and hoping for a cure.

  • Transplant is less risky than gene therapy and is available now. It is limited by ability to get a donor, but it can be an answer for some patients. People do not always need to stay on life-long immune suppression (incorrectly reported in your article). I have seen patients cured of sickle cell. It is wonderful. See CTN 1503–transplant in young adults with sickle cell. Not everyone can wait until gene therapy or a new drug is available.

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