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When Kaitlyn Sinnamon was 20 weeks pregnant with her second child, doctors told her that her baby would be born with a heart defect that would require surgery at the beginning of his life.
Easton Sinnamon was born at Duke University Hospital with single ventricle heart disease, which meant his heart had only one ventricle, instead of two, to pump blood to the rest of his body.
After two heart surgeries couldn’t correct a leaking heart valve related to his congenital heart disease, it became clear to his surgical team that Easton would need a new heart. But the transplant would require Easton to be on immune-suppressing medications for the rest of his life so his body wouldn’t reject the new organ.
These medications can increase the risk of cancer and be toxic to the kidneys, as well as making patients more susceptible to severe infections.
But doctors ran into another challenge while Easton awaited a heart transplant. After repeated infections, further testing revealed that he had a deficiency in a specific type of immune system cell called the T cell. T cells mature in the thymus, an organ that sits in front of the heart.
Easton’s poor immune function meant his body did not naturally make T cells, which are also often responsible for the body rejecting and attacking a transplanted organ when it doesn’t recognize it.
“It was serendipitous in the sense that Easton needed both a heart transplant and he also had very poor immune function,” said Dr. Joseph Turek, chief of pediatric cardiac surgery at Duke University and a member of Easton’s surgical team, in a news conference Monday.
This made Easton a candidate for a novel surgery to receive both a new heart and a processed thymus from the same donor. This combination of procedures had never been done on a human.
For Easton’s parents, Kaitlyn and Brandon Sinnamon, the decision to have their baby undergo such critical procedures wasn’t an easy one, especially given the risks that come with transplant surgery. When Easton’s second surgery failed, Turek discussed the options with the Sinnamons. CNN
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“I think one thing that stuck with us the most is, he told us, ‘I want to give you your son back, and the only way I can do that is through transplant,’ ” Kaitlyn Sinnamon told CNN. ” ‘If it works, not only is that going to help Easton, but it’s going to help millions of other people, as well. And on top of that, we get to make a huge difference. And if it doesn’t work, we at least tried it.’ ”
According to Turek, Duke University is the only place in the Western Hemisphere that does cultured thymus transplants, in which donor thymus cells are incubated and grown in a lab before being implanted in the recipient.
In a healthy immune system, immature immune cells enter the thymus, where they learn to identify what is “self” and what is foreign. The process of culturing the thymus clears any of the donor’s mature immune cells, leaving a scaffold of a thymus for the recipient to develop their own immune cells through.
“It’s the idea that the thymus is growing up in the same environment as the new transplanted organ is what allows it to recognize it as ‘self.’ If you just use the thymus and didn’t culture it, you already have cells that would start to reject,” Turek told CNN.
Easton’s immune deficiency meant he might be able to develop one aspect of his immune system — T cells — while his body grew accustomed to his new heart. This double transplant from the same donor could even eliminate the need for dangerous lifelong immune-suppressing medication.
In August, at 6 months old, Easton got his heart transplant and was started on immune-suppressing medication. Two weeks later, after the donor thymus cells had completed the culture process, he also received the thymus implantation.
“It’s bittersweet to be excited about your child getting a transplant because you get to bring your child home, but someone else is losing theirs,” Sinnamon said.
Shortly after his surgery, Easton was moved out of the intensive care unit, which indicated to his parents that he was recovering well.
Six months post-transplant, testing demonstrated that Easton’s new thymus was properly developing T cells and that his body had not rejected his new heart. These results are promising, and Easton’s medical team hopes to wean him off his immune-suppressing medication in a year if tests confirm that his T cells recognize his transplanted heart as his own.
“The idea that you could have a transplant and not have to be on these medications is really a … game-changer for patients with transplanted organs,” Turek told CNN
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