Reposted from U of U Health.

A new gene therapy can reverse the effects of heart failure and restore heart function in a large animal model, according to new research from the University of Utah. The therapy increases the amount of blood the heart can pump and dramatically improves survival, in what the study calls “an unprecedented recovery of cardiac function.”

Currently, heart failure is irreversible. In the absence of a heart transplant, most medical treatments aim to reduce the stress on the heart and slow the progression of the often-deadly disease. But if the gene therapy shows similar results in future clinical trials, it could help heal the hearts of the one in four people alive today who will eventually develop heart failure.

The results were published on Dec. 10 in npj Regenerative Medicine.

A “night and day” change

The researchers were focused on restoring a critical heart protein called cardiac bridging integrator 1 (cBIN1). They knew that the level of cBIN1 was lower in heart failure patients—and that, the lower it was, the greater the risk of severe disease.

“When cBIN1 is down, we know patients are not going to do well,” said Robin Shaw, director of the U’s Nora Eccles Harrison Cardiovascular Research and Training Institute (CVRTI) a co-senior author of the study. “It doesn’t take a rocket scientist to say, ‘What happens when we give it back?’”

To try and increase cBIN1 levels in cases of heart failure, the scientists turned to a harmless virus commonly used in gene therapy to deliver an extra copy of the cBIN1 gene to heart cells. They injected the virus into the bloodstream of pigs with heart failure. The virus moved through the bloodstream into the heart, where it delivered the cBIN1 gene into heart cells.

For this heart failure model, heart failure generally leads to death within a few months. But all four pigs that received the gene therapy in their heart cells survived for six months, the endpoint of the study.

Importantly, the treatment didn’t just prevent heart failure from worsening. Some key measures of heart function actually improved, suggesting the damaged heart was repairing itself.

“In the history of heart failure research, we have not seen efficacy like this,” Shaw said. Previous attempted therapies for heart failure have shown improvements in heart function on the order of 5 to 10%. cBIN1 gene therapy improved function by 30%. “It’s night and day,” Shaw added.

The treated hearts’ efficiency at pumping blood, which is the main measure of the severity of heart failure, increased over time—not to fully healthy levels, but too close to that of healthy hearts. The hearts also stayed less dilated and less thinned out, closer in appearance to that of non-failing hearts. Despite the fact that, throughout the trial, the gene-transferred animals experienced the same level of cardiovascular stress that had led to their heart failure, the treatment restored the amount of blood pumped per heartbeat back to entirely normal levels.

“Even though the animals are still facing stress on the heart to induce heart failure, in animals that got the treatment, we saw the recovery of heart function and that the heart also stabilizes or shrinks,” said TingTing Hong, associate professor of pharmacology and toxicology and CVRTI investigator and co-senior author. “We call this reverse remodeling. It’s going back to what the normal heart should look like.”

A keystone of the heart

The researchers think that cBIN1’s ability to rescue heart function hinges on its position as a scaffold that interacts with many of the other proteins important to the function of heart muscle.

“cBIN1 serves as a centralized signaling hub, which actually regulates multiple downstream proteins,” said Jing Li, associate instructor at CVRTI. By organizing the rest of the heart cells, cBIN1 helps restore critical functions of heart cells. “cBIN1 is bringing benefits to multiple signaling pathways.”

Indeed, the gene therapy seemed to improve heart function on the microscopic level, with better-organized heart cells and proteins. The researchers hope that cBIN1’s role as a master regulator of heart cell architecture could help cBIN1 gene therapy succeed and introduce a new paradigm of heart failure treatment that targets the heart muscle itself.

Along with industry partner TikkunLev Therapeutics, the team is currently adapting the gene therapy for use in humans and intends to apply for FDA approval for a human clinical trial in the fall of 2025. While the researchers are excited about the results so far, the therapy still has to pass toxicology testing and other safeguards. And, like many gene therapies, it remains to be seen if it will work for people who have picked up a natural immunity to the virus that carries the therapy.

But the researchers are optimistic.

“When you see large animal data that’s really close to human physiology, it makes you think,” Hong said. “This human disease, which affects more than 6 million Americans—maybe this is something we can cure.”

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These results were published on Dec. 10 as “Cardiac Bridging Integrator 1 Gene Therapy Rescues Chronic Non-ischemic Heart Failure in Minipigs” in npj Regenerative Medicine.

• Sophia Friesen Manager, Science Communications, University of Utah Health
  ‭(510) 495-7528‬ sophia.friesen@hsc.utah.edu