Scientists print human liver tissue in breakthrough that could save lives (opens in new tab)

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Looking ahead: Every year, tens of thousands of Americans receive organ transplants, yet demand still outstrips supply. Now, a research team at Carnegie Mellon University believes the way out of that crisis may not be more donor organs but engineered ones – built layer by layer through bioprinting.

The university’s scientists have received a $28.5 million award from the Advanced Research Projects Agency for Health to develop a transplantable 3D-printed liver patch. The initiative – known as the Liver Immunocompetent Volumetric Engineering (LIVE) project – aims to create living liver tissue that can temporarily take over core functions, giving a failing organ enough time to regenerate.

Instead of replacing the liver, the engineered tissue would support it for about two to four weeks, buying crucial time and reducing the need for full transplants.

At the center of the work is the Freeform Reversible Embedding of Suspended Hydrogels, or FRESH, platform. Developed at Carnegie Mellon, FRESH allows researchers to print soft biological materials – such as collagen and living cells – into finely detailed, three-dimensional scaffolds that mimic complex human tissue structures.

FRESH 3D bioprinted perfusable liver tissue inside of a bioreactor.

Earlier studies by the same lab demonstrated that FRESH can produce vascularized pancreatic-like tissue, showing the system’s potential to model diseases such as Type 1 diabetes. The new challenge is scaling that approach to something much larger and more functionally demanding: the liver.

Unlike approaches that rely on genetically modified pig organs, the Carnegie Mellon project begins entirely with human biological materials. The printed tissues incorporate hypoimmune cells – engineered to act as universal donors – along with human collagens and other structural proteins.

The goal is to make the tissue inherently immune-compatible so that recipients do not need to take immunosuppressant drugs. "The challenge is really the immune system," said project lead Adam Feinberg. "We are going to be using hypoimmune cells, which are engineered to be universal donors, so anyone can have the cells and tissues we are building without needing to take immune suppression."

The wider field of transplantation research is moving in several directions at once. Recent advances include reviving organs after death using perfusion systems that restore circulation and oxygen, and extending the viability of donor organs outside the body.

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