Help for patients with sickle cell disease may soon come from gene editing to fix the mutation that causes the disease and boost the patient's own protective fetal hemoglobin. New research shows that using CRISPR-Cas9 and a corrective short DNA template to repair the sickle cell mutation in a patient's hematopoietic stem cells (HSCs) could be efficient and safe.
Bioengineer Gang Bao of Rice University's Brown School of Engineering conducted the research in collaboration with Texas Children's Hospital, Baylor College of Medicine and Stanford University. The revelation is one of several in a new study led by Bao and Vivien Sheehan, an assistant professor at Baylor and a member of the sickle cell program at Texas Children's Hematology Center. The open-access study appears in the Oxford Academic journal Nucleic Acids Research.
Today, some people afflicted with the sickle cell disease are treated with stem cells from a matched, related donor, an option researchers says is available to fewer than 15 percent of patients. A better strategy would be modifying the patient's own hematopoietic stem and progenitor cells (HSPCs), an option theoretically available to every patient because there would be no risk of rejection.
Ideally, stem cells isolated from the patient's bone marrow would be gene-edited and tested, and chemotherapy would be used to reduce the patient's stem cells to make room for the edited cells. Bao said the corrected cells would then be implanted back into the patient, where they could proliferate and spawn healthy blood cells.
For the new study, and for the first time, Bao and his team tested patient HSPCs in rodents and demonstrated that a fraction of the gene-edited cells from patients could survive and function for about 4 months.
These stem cells were from the peripheral blood of five patients and the bone marrow of two patients with the disease, all obtained by Sheehan. The Sheehan lab characterized the type of hemoglobin made by the edited cells and showed that gene editing can provide enough protective and normal hemoglobin to prevent sickling, even under the severe hypoxia that promotes sickling.
Early tests using wild-type Cas9 protein—the "scissors" that target and cut specific sections of DNA—from Streptococcus pyogenes led to stem cells with high levels of unintended DNA edits. These off-target edits included large chromosomal deletions and inversions that could cause disease.
In a second round of tests, the Rice lab adopted a more recent "high-fidelity" version of Cas9 developed by Integrated DNA Technologies. That led to significantly reduced off-target edits, Bao said.
Not all the stem cells isolated from a patient with the sickle mutation are fixed by gene editing. At best, according to experiments by the Bao lab, it fixed up to 40 percent of them. In another 50 percent of cells, DNA was cut and not repaired by the corrective DNA template, but that appeared to boost the stem cells' expression of fetal hemoglobin (HbF), a type made by a different gene that does not carry the sickle mutation and is normally turned off a few months after birth.
Fetal hemoglobin is known to mute the effects of sickle cell disease. Bao suspects that if the expression of fetal hemoglobin in edited cells persists, 90 percent of the stem cells from patients will either have the sickle mutation fixed, or have sickling prevented by fetal hemoglobin.
"Our hope is that if we take out a fraction of HSPCs from a patient's bone marrow and damage the remaining ones, then edit the HSPCs and deliver them back, the combination of gene-corrected and HbF-expressing cells will be enough to cure the disease," Bao said.
