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For This Sickle Cell Patient, CRISPR Study Gives Hope

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Victoria Gray was diagnosed with sickle cell disease when she was an infant. She was considering a bone marrow transplant when she heard about the CRISPR study and jumped at the chance to volunteer. (Meredith Rizzo/NPR)

Victoria Gray is waiting patiently in a hospital room at the Sarah Cannon Research Institute in Nashville.

“It’s a good time to get healed,” she says. The 34-year-old from Forest, Miss., has struggled with sickle cell disease throughout her life.

Gray is at the hospital because she volunteered for one of the most anticipated medical experiments in decades: the first attempt to use the gene-editing technique CRISPR to treat a genetic disorder in the U.S.

She’s the first patient ever to be publicly identified as being involved in such a study.

“I always had hoped that something will come along,” Gray says in an exclusive interview with NPR. “It is just amazing how far things have come. I just want to kind of help bring awareness to this disease and let other people know that there is hope.”


Sickle cell affects millions of people around the world. About 100,000 are in the U.S., and most of them, like Gray, are African American. A genetic defect causes bone marrow to produce a defective protein that makes blood cells that are sickle-shaped, hard and sticky. The deformed cells get stuck inside blood vessels and don’t carry oxygen normally, causing a host of debilitating and, often, eventually life-shortening complications.

“It’s horrible,” Gray says. “When you can’t walk or lift up a spoon to feed yourself, it gets real hard.”

For the study, doctors are using cells taken from patients’ own bone marrow that will be genetically modified with CRISPR to make them produce a protein that is usually only made by fetuses and by babies for a short time following birth.

The hope is this protein will compensate for the defective protein that causes sickle cell disease and enable patients to live normally for the rest of their lives.

“It’s exciting to see that we might be on the cusp of a highly effective therapy for patients with sickle cell,” says Dr. David Altshuler, executive vice president, global research and chief scientific officer at Vertex Pharmaceuticals in Boston. Vertex is co-sponsoring the study with CRISPR Therapeutics of Cambridge, Mass.

“People with sickle cell disease have been waiting a long time for therapies that just let them live a normal life,” Altshuler says.

“This is a very big deal,” agrees Dr. Haydar Frangoul, medical director of pediatric hematology/oncology at the institute where Gray volunteered. “This could benefit many patients.”

Frangoul’s center, Sarah Cannon, is conducting the study at HCA Healthcare’s TriStar Centennial Medical Center in Nashville, which is one of eight sites recruiting patients for the research in the United States, Canada and Europe. Up to 45 patients ages 18 to 35 will eventually be enrolled.

Other doctors, scientists and bioethicists are also encouraged.

“This is an exciting moment in medicine. CRISPR promises the capacity to alter the human genome and to begin to directly address genetic diseases,” says Laurie Zoloth, a bioethicist at the University of Chicago.

But Zoloth is also cautious. She worries that this and other studies starting up using CRISPR haven’t gone through an extra layer of scrutiny by a panel of outside experts assembled by the National Institutes of Health.

“This a brand-new technology,” Zoloth says. “It seems to work really well in animals and really well in culture dishes. It’s completely unknown how it works in actual human beings. So there are a lot of unknowns. It might make you sicker.”

Frangoul acknowledges there are always risks with experimental treatments. But, he says, the research will go very slowly and carefully with close review by the Food and Drug Administration and other advisory panels.

“We are very cautious about how we do this trial in a very systematic way to monitor the patients carefully for any complications related to the therapy,” he says.

For her part, Gray says she understands there are risks. She also says that she knows the study is a first step and that other patients might only see benefits years from now.

“This gives me hope if it gives me nothing else,” Gray says.

It will probably take several months before doctors detect the first signs of whether the genetically edited cells are producing helpful levels of the protein and even longer to know whether the cells are improving patients’ health. And it will likely be take many years to know whether the benefits last a lifetime, as hoped.

Gray, who is married and has four children, was diagnosed with sickle cell disease when she was an infant and started crying during a bath. One major symptom is agonizing, debilitating pain.

Like many sickle cell patients, her symptoms have prevented her from living a full life. She couldn’t play like other children, was afraid to travel and had to give up her dreams of becoming a doctor or a nurse.

“Sometimes it feels like lightning strikes in my chest and real sharp pains all over,” Gray says. “Sometimes, I will be just balled up and crying, not able to do anything for myself.”

The defective blood cells also increase the risk for infections and damage to vital organs such as the heart. They also can cause life-threatening strokes. Many people with sickle cell disease don’t live past their 40s. Gray’s heart has already suffered damage. And that is taking an additional psychological toll.

“It’s scary,” she says, describing how her disease has affected her oldest son, 12-year-old Jamarius.

“He’s older, so he understands. So he started acting out in school. And his teacher told me, ‘I believe Jamarius is acting out because he really believes you’re going to die,’ ” Gray says, choking back tears.

Some patients can get bone marrow transplants, but those procedures are grueling and can be dangerous if the immune system cells produced by the transplanted bone marrow attack their bodies. And most sickle cell patients either don’t have or don’t find a suitable donor.

“It’s real hard,” Gray says. “It was just my religion that just kept me going.”

When she was considering a bone marrow transplant, she heard about the CRISPR trial and jumped at the chance to volunteer.

“I always knew something had to come along and that God had something important in store for me,” Gray says. “It felt like this was meant to be. It was kinda fate. That was an amazing feeling.”

CRISPR enables scientists to make very precise changes in DNA, raising hopes it will lead to new ways to prevent and treat many diseases.

“CRISPR technology has a lot of potential use in the future, not only in blood disorders,” Frangoul says.

Doctors have already started using it to try treat cancer, mostly in China. At least two patients in the U.S. have been treated for cancer, in a study at the University of Pennsylvania in Philadelphia.

Later this year, doctors in Boston are planning to use CRISPR to edit cells in patients’ retinas, in hopes of restoring vision in patients with an inherited form of blindness.

The companies sponsoring the sickle cell study announced earlier this year that they had used CRISPR to treat the first patient with a similar blood disorder, beta thalassemia, in Germany.

Beta thalassemia and sickle cell disease are both caused by genetic defects that cause problems with a protein called hemoglobin. Healthy red blood cells use hemoglobin to carry oxygen throughout the body.

Sickle cell patients’ red blood cells carry defective hemoglobin that deform the cells and don’t transport enough oxygen. The hope is that another form of hemoglobin, known as fetal hemoglobin, will compensate for the defective protein.

Fetal hemoglobin is produced by fetuses in the womb to provide oxygen. In most people, fetal hemoglobin production stops shortly after birth.

“Once a baby is born, a switch will flip on,” Frangoul says. “It’s a gene that tells the red blood cell — the bone marrow cells that produce red cells — to stop making fetal hemoglobin.”

This CRISPR treatment starts with doctors extracting bone marrow cells from patients’ blood. Company scientists then use CRISPR to edit a gene in the cells to make the cells produce fetal hemoglobin.

“That will help the cells make more fetal hemoglobin and make them happier and healthier,” Frangoul says.

The patients then undergo the same kind of grueling chemotherapy administered as part of a standard bone marrow transplant. That wipes out the existing cells that are carrying the genetic defect. But instead of receiving new cells from a donor, the patients get billions of their own cells that have been edited with CRISPR.

The hope is that it will provide a treatment option for all patients, including those who can’t find a matched donor. The approach hopefully will be safer because the cells come from patients’ own bone marrow. So they shouldn’t attack patients’ bodies, Frangoul says.

“This opens the door for many patients to potentially be treated and to have their disease modified to be mild” and to avoid the “horrible, horrible long-term side effects of sickle cell disease,” he says.

Gray hopes it works and describes how she imagines a life without sickle cell:

“Being able to wake up and not be in pain. And to just be tired because I’ve done something — and not just tired for no reason. And just to be outside, and jump on the trampoline with my kids.


“And go to graduations and weddings. And see them grow up. That means the world to me.”

Copyright 2019 NPR. To see more, visit https://www.npr.org.

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