That has doctors and researchers eager to find ways to improve the process and prevent or reduce post-transplant issues.

Swapnil K. Sonkusare of UVA’s Department of Molecular Physiology and Biological Physics, led the team that identified celluar changes that contribute to the injuries to lung tissue after transplants. (Contributed photo)

A team, led by Swapnil K. Sonkusare of UVA’s Department of Molecular Physiology and Biological Physics, identified cellular changes within the lung following a transplant that contribute to an “ischemia-reperfusion injury,” a major cause of organ rejection and death after transplant. The injury occurs when blood supply returns to tissue after it has undergone a period without oxygen.

Sonkusare and his team found that by targeting the underlying biological processes, doctors may be able to prevent ischemia-reperfusion injuries.

“Our collaborative studies with Dr. Victor Laubach from [UVA’s Department of] Surgery show a new mechanism for lung ischemia-reperfusion injury,” Sonkusare, of UVA’s Robert M. Berne Cardiovascular Research Center, said. “This mechanism could be targeted to improve the clinical success of lung transplantation.”

Better Lung Transplants

Ischemia-reperfusion injury is a major cause of what is known as “primary graft dysfunction,” the leading cause of death within 30 days of a lung transplant. It also can lead to chronic allograft dysfunction, the leading cause of death a year or more after transplant. Half of lung transplant recipients develop chronic allograft dysfunction within five years of transplant, according to the National Institutes of Health.

At least some degree of ischemia-reperfusion injury is inevitable for patients who have organ transplants. Tissues are traumatized when they are disconnected from their original blood supply and reconnected to a new one. For lung transplants, this trauma can result in harmful inflammation, leaky blood vessels, damage to the tiny sacs responsible for oxygen exchange and other problems. 

Dr. Victor Laubach from UVA’s Department of Surgery is collaborating with Sonkusare and his team to develop processes to reduce the impact of lung ischemia-reperfusion injury. (Contributed photo)

While the phenomenon of ischemia-reperfusion injury is well known, researchers have struggled to understand the underlying causes. Sonkusare’s new work provides answers, identifying a particular pathway of biological processes triggered by ischemia-reperfusion. These processes occurred in endothelial cells that line blood vessels in the lung and resulted in immune cell activation leading to lung injury, UVA researchers say.

UVA scientists found blocking key steps in this pathway prevented inflammation and lung damage in lab mice, suggesting a promising approach for preventing the same problems in human transplant recipients, though much more research will be needed.

“Our collaborative research with Dr. Laubach has revealed the cellular mechanisms for lung ischemia-reperfusion injury,” Sonkusare said. “We are currently testing the effectiveness of drug molecules that block these mechanisms in various models of lung injury after transplantation, with the ultimate goal of improving the success rate of lung transplantation.”

Findings Published

The researchers have published their findings in the journal Science Signaling. The research team consisted of Maniselvan Kuppusamy, Huy Q. Ta, Hannah N. Davenport, Abhishek Bazaz, Astha Kulshrestha, Zdravka Daneva, Yen-Lin Chen, Philip W. Carrott, Laubach and Sonkusare. Sonkusare and Laubach hold a provisional patent related to targeting the processes involved in lung ischemia-reperfusion injury.

The research was supported by the National Institutes of Health, grants R01HL157407, R01HL142808, R01HL146914 and R01HL167208.

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