A clinical trial to test how genetically engineered cells might restore insulin function and reduce the need for immunosuppression in patients with type 1 diabetes has been funded.
A world-first clinical trial to test a gene therapy for type 1 diabetes, developed at the Garvan Institute of Medical Research, will proceed thanks to a Medical Research Future Fund boost from the Australian Government’s Targeted Translation Research Accelerator program for diabetes and cardiovascular disease.
The trial will be the first time that genetically engineered pancreatic islet cells will be transplanted into humans to treat type 1 diabetes.
Type 1 diabetes is an autoimmune disease often first diagnosed in childhood and adolescence. Around 125,000 Australians live with the disease, which has serious long-term health impacts, including eye damage, nerve damage, kidney disease and lower life expectancy.
There is currently no cure, and management involves daily glucose monitoring and insulin administration.
If successful, the new therapy will reduce or eliminate dependency on external insulin administration and reduce serious health impacts, which would be a game changer for type 1 diabetes management.
“We’ve worked on this research for 20 years and to see it now reach a stage of translating to people is amazing,” says lead researcher Professor Shane Grey, Head of the Transplantation Immunology lab at Garvan Institute. “It’s the beginning of a long journey, but it’s an exciting step.”
The goal for type 1 diabetes: normal islet cells
While the cause of type 1 diabetes remains unclear, the condition occurs when the body’s immune system attacks its own islet cells in the pancreas, which are responsible for sensing the concentration of sugar in the blood and producing the hormone insulin.
Insulin controls blood-sugar levels by signalling the body to convert sugar (glucose) into energy for cells. With insufficient insulin, sugar levels rise unchecked (hyperglycaemia), which can lead to complications such as nerve and blood vessel damage if untreated. Treatment with insulin can result in very low blood-sugar levels (hypoglycaemia), which can lead to seizures and loss of consciousness.
Transplant treatments of donor pancreatic islet cells into the liver have been successful in patients experiencing severe episodes of hypoglycaemia, reducing their reliance on insulin injections; however, two to three transplants are needed and the effectiveness of the transplanted islet cells usually subsides within five years.
In addition, immunosuppression medication is required to turn down the immune system so it won’t destroy the donor cells, but that leaves a patient vulnerable to serious side effects, including infections and kidney damage.
“The holy grail is to make islet cells that the body adopts as its own, which function normally to sense glucose and produce the appropriate amount of insulin,” says Professor Grey.
Key protein turns the immune system up or down
Professor Grey and team identified that a key protein known as A20, involved in inflammation and autoimmune disorders, could be used in the genetic engineering of insulin-producing islet cells to slow or stop the immune system from damaging them.
“A20 is like a thermostat for the immune system; it can turn it down to a simmer, or ramp it up to be more aggressive,” says Professor Grey. “For type 1 diabetes, we can use it as a handbrake on the immune system to stop the damage to pancreatic islet cells.”
To engineer islet cells with high expression of A20, Professor Grey and team developed a viral delivery system called GARV-AAV2-A20, which transports the gene that makes A20 into donor islet cells, which then start making higher levels of A20.
Pre-clinical trials of the cells in animal models have been highly successful.
“We showed that genetically engineered islet cells with high A20 expression in mouse models had 80-100% survival of the islet grafts, without the need for heavy immunosuppression,” says Professor Grey. “It was a fantastic outcome.” A further study in pig and human cells showed A20-engineering of islet cells was safe.
The team also discovered that not only does A20 turn down the immune system, but it helps the immune system recognise the donor islet cells as its own. “The genetically engineered cells seem to re-educate the immune system to accept the transplant as self. It’s a really amazing discovery – that the transplant can tweak the whole immune system,” says Professor Grey.
New trial could be a game-changer for type 1 diabetes
For patients, the new treatment could significantly improve their quality of life.
Dr Dorota Pawlak, Chief Scientific Officer at JDRF Australia, says, “This is an important research avenue, investigating a novel gene therapy approach with the potential to advance islet transplantation.”
“It is a globally unique project and could make islet transplantation safer and more accessible to those living with type 1 diabetes, which could drastically change how they are able to manage their condition.”
The clinical trial is a collaborative project with clinical lead Professor Toby Coates, Head of Islet Transplantation, Royal Adelaide Hospital, together with Beta Cell Technologies Pty Ltd, and gene therapy expert Professor Ian Alexander, from Children’s Medical Research Institute and Sydney Children’s Hospital Network, who is also co-lead of the Viral Vector Manufacturing Facility. The Viral Vector Manufacturing Facility project, located at the Westmead Health and Innovation Precinct, is a collaboration between NSW Treasury, Investment NSW, and various NSW Health entities, including Health Infrastructure, Office of Health and Medical Research, Sydney Children’s Hospitals Network and with support from Children’s Medical Research Institute and Western Sydney Local Health District.
Production of GARV-AAV2-A20 will begin over the next months at the Viral Vector Initiative, and patients will be recruited through the Royal Adelaide Hospital in mid-2024.
Professor Grey is Conjoint Professor, St Vincent’s Clinical School, Faculty of Medicine, UNSW Sydney; Conjoint Associate Professor, Discipline of Medicine, Faculty of Health Sciences, University of Adelaide, South Australia; and Visiting Scientist & Consultant, Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, South Australia.
This clinical trial is funded by the Medical Research Future Fund from the Australian Government’s Targeted Translation Research Accelerator program for diabetes and cardiovascular disease, delivered by MTPConnect. This research was also supported by Twin Towns Services Community Foundation Limited.
JDRF Australia, the largest non-government funder of type 1 diabetes research globally, supported early stages of research into A20 and funded the initial exploration of the role of A20 in islet survival.