Personalized tissue-engineered veins – long term safety, functionality and cellular transcriptome analysis in large animalsShow others and affiliations
2023 (English)In: Biomaterials Science, ISSN 2047-4830, E-ISSN 2047-4849, Vol. 11, no 11, p. 3860-3877Article in journal (Refereed) Published
Abstract [en]
Tissue engineering is a promising methodology to produce advanced therapy medicinal products (ATMPs). We have developed personalized tissue engineered veins (P-TEV) as an alternative to autologous or synthetic vascular grafts utilized in reconstructive vein surgery. Our hypothesis is that individualization through reconditioning of a decellularized allogenic graft with autologous blood will prime the tissue for efficient recellularization, protect the graft from thrombosis, and decrease the risk of rejection. In this study, P-TEVs were transplanted to vena cava in pig, and the analysis of three veins after six months, six veins after 12 months and one vein after 14 months showed that all P-TEVs were fully patent, and the tissue was well recellularized and revascularized. To confirm that the ATMP product had the expected characteristics one year after transplantation, gene expression profiling of cells from P-TEV and native vena cava were analyzed and compared by qPCR and sequencing. The qPCR and bioinformatics analysis confirmed that the cells from the P-TEV were highly similar to the native cells, and we therefore conclude that P-TEV is functional and safe in large animals and have high potential for use as a clinical transplant graft.
Place, publisher, year, edition, pages
Royal Society of Chemistry, 2023. Vol. 11, no 11, p. 3860-3877
National Category
Cell and Molecular Biology
Research subject
Bioinformatics
Identifiers
URN: urn:nbn:se:his:diva-22436DOI: 10.1039/d2bm02011dISI: 000972824700001PubMedID: 37078624Scopus ID: 2-s2.0-85160870522OAI: oai:DiVA.org:his-22436DiVA, id: diva2:1752117
Funder
Vinnova, 2017-02130Knowledge Foundation, #2016-0330, #2020-0014
Note
CC BY 3.0
First published 13 Apr 2023
Joakim.hakansson@ri.se
This study was supported by Vinnova project CAMP (contract no. 2017-02130), a common call by VINNOVA and Vetenskapsrådet: Biologcal pharmaseuticals (Dnr 2017-02983), by University of Skövde under grants from the Swedish Knowledge Foundation [#2016-0330, #2020-0014] and Västra Götalandsregionen (consultant check). The company VERIGRAFT AB holds a patent on peripheral whole blood perfusion of decellularized tissues and did also finance the project. We want to acknowledge the staff at the Department of Experimental Biomedicine at Gothenburg University. The swine studies in Spain were conducted by the ICTS ‘NANBIOSIS’, specifically Units 21, 22, and 24 of the CCMIJU. Graphical Abstract image created with BioRender.com.
2023-04-202023-04-202023-07-14Bibliographically approved