March 2025

From Printer to Patient: The Bioprinting Revolution in Medicine
Written by: Robin Sieg & Prof. Dr. Kathrin Adlkofer
Regenerative medicine holds the promise of repairing or replacing damaged tissues and organs, offering hope to patients with conditions once deemed irreversible. A major driving force behind this promise is 3D bioprinting – an emerging technology that constructs living tissues layer by layer using “bioinks” made of cells and biomaterials. This approach is poised to address one of healthcare’s most urgent challenges: the severe shortage of donor tissues and organs. Today, demand far outstrips supply; by some estimates, only about 10% of the global need for organ transplants is currently being met¹. Patients on transplant waitlists often have no alternative treatments, highlighting the pressing need for new solutions. This is where 3D bioprinting is making a transformative impact. By enabling the fabrication of tissues on demand, tailored to the patient, 3D bioprinting is reshaping the future of transplants, wound healing, and personalized medicine.
Beyond alleviating shortages, bioprinting offers personalization that traditional grafts cannot. Tissues can be printed using a patient’s own cells, minimizing the risk of immune rejection and potentially eliminating the need for lifelong immunosuppressive drugs. Moreover, bioprinting opens doors to innovative therapies – from printing skin patches for burn victims to creating functional organ prototypes for research and drug testing. As the technology rapidly advances, what once sounded like science fiction is becoming a practical tool in the clinician’s arsenal. In the following sections, we’ll explore how 3D bioprinting works, the breakthroughs happening right now (including ambitious projects in Europe aiming to print everything from corneas to colon tissue), and what it all means for the future of healthcare.
3D bioprinting adapts the principles of 3D printing to living biology. Instead of plastic or metal, “bioink” made of living cells and supportive biomaterials is printed layer-by-layer to create tissues. Several bioprinting techniques have been developed, primarily falling into three categories: inkjet (droplet-based), extrusion (pressure-assisted), and laser-assisted bioprinting. Each method uses a different mechanism to deposit cells precisely, but they share the same goal – to assemble cells into structures that mimic natural tissue architecture.² Often a scaffold or hydrogel is printed along with the cells to help them keep their shape and to provide an environment where they can survive and mature. With these approaches, researchers have already printed a variety of tissue types in the lab, including skin, bone, cartilage, and even tiny heart tissues. Crucially, what gets printed is not yet a fully functional organ – it’s typically a tissue construct that needs time (and often bioreactors or incubation) to develop.
This is sometimes referred to as 4D bioprinting, adding the fourth dimension of time, where a printed structure is designed to undergo natural cell growth, tissue maturation, or even programmed shape-change after printing. By combining smart biomaterials (that might dissolve or change shape) with living cells, 4D bioprinting aims to create tissues that develop post-printing into the form and function needed. In practice, once a tissue is printed in 3D, it is often cultured to allow cells to multiply, secrete their own matrix, and organize into a structure that can integrate with the human body. This ability to control not just the initial shape of a tissue, but its maturation process, is a powerful aspect of bioprinting technology – one that is continually improving as we learn to better mimic the body’s developmental cues.
From Lab to Clinic: Bioprinted Tissues Making Strides
The first targets of bioprinting are relatively simple tissues that could make a big impact. For example, bioprinted skin patches are being developed to heal wounds and burns. An NIH-funded team recently showed that a 3D bioprinted skin substitute can effectively close large wounds in preclinical models, suggesting a promising alternative to painful skin graft surgeries. Their portable bioprinter lays down layers of a patient’s own skin cells directly into the wound, forming new skin that includes all the essential layers and cell types of normal skin. Such advances raise hope that severe burns might one day be treated with printed skin, sparing patients from donor site surgeries and extensive scarring. Bone tissue is another focus area. Scientists have created bioprinted bone grafts by printing scaffolds infused with stem cells to repair bone defects.
In one recent case, doctors bioprinted a personalized bone implant using a patient’s own cells (from platelet-rich plasma) combined with a bioceramic scaffold, and used it to successfully replace a section of the patient’s tibia lost to a tumor. This tailored, living bone graft integrated with the patient’s body, demonstrating how 3D bioprinting could transform bone reconstruction surgeries in the future. Bioprinted bone substitutes might help treat complex fractures or bone diseases without the complications of taking bone from another part of the patient’s body or using synthetic implants. Researchers are even printing miniature organs (“organoids”) and organ parts for research and therapeutic development. A striking example is the bioprinting of mini-hearts.
In 2019, a team at Tel Aviv University bioprinted a tiny heart complete with cells and blood vessels – the first time a vascularized heart was printed entirely from patient-derived cells. The printed heart was only about the size of a rabbit’s heart and too small to transplant, but it beat in the lab and showcased the incredible complexity that bioprinting can achieve. Mini-organs like this serve as important models to test new drugs and study diseases. Likewise, researchers have printed liver tissue that can perform basic liver functions and kidney tissue that mimics filtration, paving the way toward printing larger, transplantable organs in the long run.

The image depicts a futuristic medical scene from Star Trek, resembling a 3D in-situ bioprinter. A patient lies beneath an advanced device, seemingly performing personalized tissue regeneration directly on the body. This vision reflects current research into in-situ bioprinting and its potential for regenerative medicine.
Pioneering Projects on the Horizon
A testament to how far bioprinting has come – and how quickly it’s moving toward real-world impact – can be seen in large collaborative initiatives. In Europe, several high-profile projects funded by programs like Horizon Europe are pushing bioprinting technology to new heights, targeting some of the most pressing medical challenges. These consortia bring together research institutions, industry leaders, and clinical experts with the shared goal of transforming how tissues and organs are created, repaired, and delivered. From orthopedics to ophthalmology, the Horizon Europe projects demonstrate how multidisciplinary collaboration can turn complex scientific visions into real-world clinical solutions.
Projects like LUMINATE, m2M, NEOLIVER, and STRONG-UR showcase the vast potential and diverse applications of bioprinting. LUMINATE focuses on repairing joint injuries by printing cartilage and bone directly into large joint defects during surgery - using a device that integrates multiple print heads and light-based curing systems. The m2M project is tackling the grand challenge of scaling up microtissue building blocks into full-sized, load-bearing grafts, offering hope for patients suffering from cartilage degeneration or spinal disc injuries. NEOLIVER is advancing the bioprinting of liver tissue, using patient-derived organoids and vascularization strategies to create implantable liver segments that could one day replace the need for full organ transplants. Meanwhile, STRONG-UR is developing tailored, bioprinted grafts to treat urethral strictures and other tubular structures in the body, using both in situ and modular implantation techniques alongside bioinks engineered for optimal integration.
Among these ambitious projects, TENTACLE (an acronym for InnovaTivE in situ 4D biopriNTing for regenerAtion of CoLorEctal mucosa and submucosa) is focusing on a novel approach to heal the gastrointestinal tract. The goal of this ambitious project is to develop technology for in situ bioprinting – that is, printing cells directly at the site of injury inside the body – to repair damage to the colon’s lining. Imagine a patient with an ulcerative lesion in the colon or one who has had a section of gut removed; the TENTACLE approach could involve a specialized bioprinter endoscope that applies new layers of cells and biomaterials right onto the defect inside the patient, precisely where needed. By using 4D bioprinting principles (so that the printed tissue continues to develop and integrate after printing), the project aims to regenerate functional intestinal tissue that can restore the integrity of the colon wall. This kind of therapy could transform outcomes for diseases like inflammatory bowel disease or colorectal cancer surgery, reducing complications and speeding up recovery by literally printing a patch inside the body to aid healing. While still in research phases, TENTACLE brings together experts in cell biology, materials science, and clinical gastroenterology, highlighting the multidisciplinary nature of bioprinting advances.
On another front, the KeratOPrinter project is zeroing in on a solution for corneal blindness. Corneal disease is a leading cause of blindness worldwide, affecting approximately 12 million people, yet only a tiny fraction of patients receive corneal transplants because donor tissue is so scarce³. KeratOPrinter’s mission is to change that equation by developing a 4D bioprinting platform for manufacturing human corneas in the lab. The idea is bold: instead of relying on eye donations, hospitals of the future could have bioprinted corneal grafts ready for patients who need them. Achieving this means overcoming several challenges – printing a curved, transparent, multi-layer tissue that can integrate into an eye is no small feat. The cornea’s structure includes organized collagen fibers and different cell types (epithelial cells on the outside, stromal cells in the middle, endothelial cells on the inner surface), all of which need to be recreated for a bioprinted cornea to function.
The KeratOPrinter consortium is tackling these issues with a comprehensive strategy: developing advanced bioinks that can form a clear, strong corneal tissue; refining high-precision printing techniques to reproduce the cornea’s delicate architecture; and ensuring that the printed corneas will be biocompatible and safe for transplantation. The project envisions a fully functional bioprinting “suite” – essentially a system that includes the bioprinter, the bioinks, and the protocols – for producing transplant-ready corneas. Notably, the KeratOPrinter project brings together experts from both academia and industry. As part of this initiative, we at Cellbox Solutions contribute our expertise in cell transport technology, ensuring that bioprinted corneas remain viable throughout their journey. From production in a centralized facility to delivery at a clinic, maintaining optimal conditions is crucial for successful transplantation. Our role focuses on securing this critical “last mile”, preserving the integrity of these delicate, lab-grown corneal grafts so they reach patients in perfect condition.
By concentrating resources and expertise on specific clinical goals, these projects are not only generating technical breakthroughs but also paving the way for regulatory and manufacturing frameworks that could bring bioprinted therapies to routine clinical use.
A New Era for Regenerative Medicine
From printing tiny patches of tissue to aspiring to print entire organs, 3D bioprinting is driving regenerative medicine into an exciting new era. The technology has matured from a lab curiosity to a platform that is actively being explored in preclinical trials and sophisticated research projects across the globe. As we’ve seen, its impact is multifaceted: offering solutions to organ and tissue shortages, enabling personalized treatments tailored to a patient’s own cells, and even transforming how we approach research and development of new therapies. Challenges remain on the road ahead. Ensuring that bioprinted tissues can establish blood flow, nerve connections, and long-term function after implantation is a significant scientific hurdle. Scaling up production and navigating the regulatory landscape for these novel, living products will also require continued innovation and collaboration between scientists, engineers, clinicians, and policymakers. Yet the progress to date is deeply encouraging.
What makes this moment especially promising is the convergence of technologies and expertise coming together to support 3D bioprinting’s success. Advances in stem cell science, biomaterials, and bioreactor cultivation provide the raw ingredients to print better tissues. Initiatives like TENTACLE and KeratOPrinter show that with the right partnerships and funding, we can tackle specific medical problems (like complex internal injuries or corneal blindness) head-on, translating printing innovations into therapeutic solutions. Meanwhile, AI-driven improvements are making the printing process smarter and more reliable every day. Together, these trends are accelerating the transition of bioprinting from the bench to the bedside.
For healthcare providers and patients, the implications are profound. We are moving toward a future where organ waitlists could shrink or even disappear – a future where a patient needing a new tissue might have one custom-made for them, and where complex injuries or degenerative diseases can be treated not just with medications, but with newly printed living parts that actually restore function. While that future is still in development, each year brings it closer to reality.
Staying engaged with these advancements is crucial. Researchers and companies worldwide, such as Cellbox Solutions and its partners, are working to solve the remaining puzzles and build the infrastructure needed to make regenerative medicine’s leap forward sustainable. At Cellbox Solutions, for instance, the focus on safe transport of living cells and tissues complements the bioprinting revolution by ensuring that once a tissue is printed, it can journey from the lab to the clinic without compromise – effectively bridging the gap between creation and transplantation. As 3D bioprinting continues to transform what’s possible, those of us in the scientific and medical community, as well as patients and stakeholders, all have a role to play in supporting and guiding its development. By fostering collaboration, encouraging smart regulation, and embracing innovation, we can help usher in a new era where repaired organs, bioengineered tissues, and personalized transplants are not the exception but the norm. The transformation of regenerative medicine is underway – and its ultimate success will mean countless lives improved and saved in the years to come.
References
² Li, J., Chen, M., & Fan, X. et al., “Recent advances in bioprinting techniques: approaches, applications and future prospects,” Journal of Translational Medicine 14, 271 (2016). (Review detailing the main categories of 3D bioprinting technologies and their uses in tissue engineering.)
³ Gain, P. et al., “Global Survey of Corneal Transplantation and Eye Banking,” JAMA Ophthalmology 134(2):167–173 (2016). (Survey reporting an estimated 12.7 million people with corneal blindness, of whom only 1 in 70 receive corneal transplants, highlighting the critical donor shortage.)
Links:
- European Commission: https://commission.europa.eu/index_en
- HaDEA: hadea.ec.europa.eu
- TENTACLE: LinkedIn
- M2m: https://m2mproject.eu/
- LUMINATE: https://cordis.europa.eu/project/id/101191804,
- STRONG-UR: https://www.strong-ur.eu/ , LinkedIn
- NEOLIVER: https://neoliver.eu/
- KeratOPrinter: https://www.keratoprinter-project.eu/ , LinkedIn

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