Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Oct;15(10):818-830.
doi: 10.1002/term.3233. Epub 2021 Aug 12.

Individualized tissue-engineered veins as vascular grafts: A proof of concept study in pig

Affiliations

Individualized tissue-engineered veins as vascular grafts: A proof of concept study in pig

Joakim Håkansson et al. J Tissue Eng Regen Med. 2021 Oct.

Abstract

Personalized tissue engineered vascular grafts are a promising advanced therapy medicinal product alternative to autologous or synthetic vascular grafts utilized in blood vessel bypass or replacement surgery. We hypothesized that an individualized tissue engineered vein (P-TEV) would make the body recognize the transplanted blood vessel as autologous, decrease the risk of rejection and thereby avoid lifelong treatment with immune suppressant medication as is standard with allogenic organ transplantation. To individualize blood vessels, we decellularized vena cava from six deceased donor pigs and tested them for cellular removal and histological integrity. A solution with peripheral blood from the recipient pigs was used for individualized reconditioning in a perfusion bioreactor for seven days prior to transplantation. To evaluate safety and functionality of the individualized vascular graft in vivo, we transplanted reconditioned porcine vena cava into six pigs and analyzed histology and patency of the graft at different time points, with three pigs at the final endpoint 4-5 weeks after surgery. Our results showed that the P-TEV was fully patent in all animals, did not induce any occlusion or stenosis formation and we did not find any signs of rejection. The P-TEV showed rapid recellularization in vivo with the luminal surface covered with endothelial cells. In summary, the results indicate that P-TEV is functional and have potential for use as clinical transplant grafts.

Keywords: biomimetics; bioreactors; in-vitro and in-vivo; regenerative medicine; scaffolds; stem cells; surface modification; tissue engineering.

PubMed Disclaimer

References

REFERENCES

    1. Boeer, U., Buettner, F. F. R., Klingenberg, M., Antonopoulos, G. C., Meyer, H., Haverich, A., & Wilhelmi, M. (2014). Immunogenicity of intensively decellularized equine carotid arteries is conferred by the extracellular matrix protein collagen type VI. Acott TS. PloS One, 9, e105964. https://doi.org/10.1371/journal.pone.0105964
    1. Böer, U., Hurtado-Aguilar, L. G., Klingenberg, M., Lau, S., Jockenhoevel, S., Haverich, A., & Wilhelmi, M. (2015). Effect of intensified decellularization of equine carotid arteries on scaffold biomechanics and cytotoxicity. Annals of Biomedical Engineering, 43, 2630-2641. https://doi.org/10.1007/s10439-015-1328-1
    1. Byrom, M. J., Bannon, P. G., White, G. H., & Ng, M. K. C. (2010). Animal models for the assessment of novel vascular conduits. Journal of Vascular Surgery, 52, 176-195. https://doi.org/10.1016/J.JVS.2009.10.080
    1. Chemla, E. S., & Morsy, M. (2009). Randomized clinical trial comparing decellularized bovine ureter with expanded polytetrafluoroethylene for vascular access. British Journal of Surgery, 96, 34-39. https://doi.org/10.1002/bjs.6434
    1. Crapo, P. M., Gilbert, T. W., & Badylak, S. F. (2011). An overview of tissue and whole organ decellularization processes. Biomaterials, 32, 3233-3243. https://doi.org/10.1016/j.biomaterials.2011.01.057

Publication types

LinkOut - more resources