A new treatment for patients with X-linked chronic granulomatous disease (CGD) fighting infections that don’t respond to intensive antibiotics could be on the horizon—but researchers need help from members of the CGD community to complete a clinical trial.
About 5% of individuals with CGD experience fungal and bacterial infections that don’t clear up with standard antibiotic therapy. In these cases, patients can be treated with healthy granulocytes—a type of white blood cell—from HLA-matched donors. This short-term treatment can help the patient get healthy enough for bone marrow transplant (BMT), a long-term treatment for CGD. However, matched donors are often in short supply. In addition, patients sometimes develop anti-HLA antibodies to the donor granulocytes, prohibiting them from receiving granulocytes in the future and increasing their risk of graft versus host disease if they opt for a BMT.
Persons with X-linked CGD have a variant in the gene for NADPH oxidase that makes their granulocytes unable to produce the hydrogen peroxide necessary to kill certain fungi and bacteria. This variant leaves those with CGD vulnerable to infection. In the clinical trial, researchers at the National Institute of Allergy and Infectious Diseases (NIAID) are testing the safety and feasibility of modifying an individual’s own granulocytes with functional NADPH oxidase messenger RNA (mRNA) as an alternative to receiving HLA-matched donor granulocytes.
The clinical trial is recruiting healthy men with X-linked CGD between the ages of 18-75 to participate. In a multi-step process, participants take medication to stimulate granulocyte production, and their extra granulocytes are then collected through apheresis. Researchers modify the granulocytes using mRNA to deliver the correct instructions for the NADPH oxidase enzyme. Participants receive the modified granulocytes the day after their apheresis and are monitored for three additional days. The hospital stay for the study is at least seven days, and there is a 3-month follow-up visit.
In the first phase of the clinical trial, two persons with CGD received the modified granulocytes. One person responded well with no side effects. The other experienced elevated liver enzymes that were possibly related to the treatment but could have also been due to antibiotics and other medications.
Unlike gene therapy, where a person’s blood-forming stem cells are modified with DNA, modifying cells with mRNA is not permanent. The eventual goal is to be able to use the procedure to treat CGD patients with severe infections, providing them with the ability to kill germs long enough to recover from the infection.
“If this [procedure] were to be demonstrated to be safe and effective, the patient would be their own granulocyte donor, so finding donors would not be a problem, and patients would not develop anti-HLA antibodies since their own neutrophils would be used,” explained Dr. Harry Malech, an investigator on the study.
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