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Implant Infused with Oxygen Maintains Insulin-Producing Cells in Rats, Absence of Immunosuppression Required

Implant that produces oxygen successfully maintains high-density insulin-producing cells in diabetic rats for extended periods, without the need for immune suppression.

Artificial Insulin Cell Sustenance in Rats through Oxygenated Implant, Absence of Immunosuppression...
Artificial Insulin Cell Sustenance in Rats through Oxygenated Implant, Absence of Immunosuppression Required

Implant Infused with Oxygen Maintains Insulin-Producing Cells in Rats, Absence of Immunosuppression Required

In a significant breakthrough for diabetes research, a new system called the BioElectronics-Assisted Macroencapsulation (BEAM) system has shown promising results in keeping insulin-producing cells alive and functional under severe hypoxia. Developed by Dr. Minglin Ma's lab in collaboration with Giner Inc., this system could revolutionize the treatment of Type I diabetes (TID).

TID is a condition where the body's immune system destroys the pancreatic Ξ²-cells that produce insulin. Currently, people with TID manage the condition through daily insulin injections or pumps, but even with treatment, the disease can lead to life-threatening complications.

The BEAM system is engineered to be immune protective and designed to last for a long time without fouling of the membrane. It combines an electrochemical oxygen generator with a scalable, linear cell pouch for continuous oxygen supply to the encapsulated cells. This continuous supply of oxygen may be vital for the long-term function of pancreatic islets in cell encapsulation systems.

In an allogeneic rat model, the oxygenated BEAM system reversed diabetes for up to three months without immunosuppression, while non-oxygenated controls remained hyperglycemic. This suggests that the BEAM system could offer an immunosuppression-free strategy to protect transplanted cells, which is imperative to fully harness the potential of cell therapy for curing TID.

The BEAM system kept rat insulinoma (INS-1) cell aggregates and primary human pancreatic islets alive and functional under severe hypoxia at a high packing density of 60,000 islet equivalents per milliliter. This is a significant achievement, as most cell replacement therapies fail due to insufficient oxygen within the encapsulated cells after implantation.

For the two million Americans with Type I diabetes, the BEAM system could someday shift cell therapy from experimental to routine care. Linda Tempelman, a key figure in the BEAM system's development, envisions broader applications for the system, including long-term treatment of conditions where the body is missing something.

The team plans to scale up to pig studies and eventually human trials. If successful, the BEAM system could bring a century-old dream of an insulin-free life closer to reality. Without insulin, the body cannot deliver glucose into muscle and tissue cells to generate energy. The BEAM system's potential to provide a sustainable source of insulin could transform the lives of those with TID.

Macroencapsulation, a strategy for cell replacement therapy, involves housing insulin-producing cells within a semipermeable device that shields them from the immune system. The BEAM system's ability to provide a continuous supply of oxygen to these encapsulated cells could make it a game-changer in this field.

Developing an immunosuppression-free strategy to protect transplanted cells is crucial for the full potential of cell therapy to be realized. The BEAM system, with its immune protective design and long-lasting functionality, could be a significant step towards achieving this goal.

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