Seattle biotech startup Immusoft has received approval to begin clinical trials of its novel strategy for treating genetic disease, the company announced Thursday. Immusoft says it’s the first to get permission to use engineered immune system cells called B cells in a human study.
The U.S. Food and Drug Administration (FDA) approved Immusoft’s Investigational New Drug Application for testing its immunotherapy for a rare, lethal childhood disease called MPS I.
An immune response includes a suite of players, and the B cells are responsible for producing the antibodies that stick to invading bacteria and viruses. The company is able to modify B cells into “biofactories” that instead crank out missing or non-functioning enzymes and proteins in the cells of patients.
“This is a huge achievement for the company and a historic moment in the field of cell and gene therapies,” said Sean Ainsworth, Immusoft’s CEO and chairman, in a statement.
Immusoft CEO Sean Ainsworth. (Immusoft Photo)
The approach has potential advantages to current strategies for delivering treatments. Therapies that use a virus as its delivery mechanism can trigger immune responses that limit their effectiveness. Treatments using stem cells can have difficulties associated with chemotherapy and stem cell transplants.
Immusoft’s technology, called ISP-001, uses a patient’s own B cells, reprogramming them to make needed proteins. Other companies working on B cell therapies include Be Biopharma and Walking Fish Therapeutics.
“I don’t know if they are going to be successful, but it’s exciting for all of us that they have gotten permission to start a trial,” researcher Richard James told MIT Technology Review. James’s lab at the University of Washington is also working on B cell engineering.