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Inventing Engineered Organoids for end-stage liver failure patients.

Authors :
Antarianto, Radiana D
Mahmood, Amer
Giselvania, Angela
Asri Dewi, Ayu AA Prima
Gustinanda, Jatmiko
Pawitan, Jeanne Adiwinata
Source :
Journal of Molecular Histology; Aug2022, Vol. 53 Issue 4, p611-621, 11p
Publication Year :
2022

Abstract

End-stage liver disease (ESLD) is a term used clinically in reference to a group of liver diseases with liver transplantation as the choice of treatment. Due to the limitations of liver transplantation, alternative treatments are needed. The use of primary human hepatocytes represents a valid alternative treatment, but the limitations related to hepatocyte quality, viability, function, conservation, and storage need to be overcome. Transplanted hepatocytes have only been followed for 6–9 months. Therefore, long-term causes of failures are not yet established, including rejection, apoptosis, or other causes. Other alternative therapies to replace liver transplantation include plasmapheresis, hemodiafiltration, and artificial livers. Unfortunately, these methods are highly limited due to availability, high cost, anaphylaxis reaction, development-deposition of immune-complexes, and restricted functionality. Liver organoids, which utilize stem cells instead of 'impractical' adult hepatocytes, may be a solution for the development of a complex bioartificial liver. Recent studies have explored the benefits of differentiating mature hepatocytes from stem cells inside a bioreactor. When the use of human-induced Hepatocytes (hiHeps) was investigated in mouse and pig models of liver failure, liver failure markers were decreased, hepatocyte function indicated by albumin synthesis improved, and survival time increased. Bioartificial liver treatment may decrease the infiltration of inflammatory cells into liver tissue by down-regulating pro-inflammatory cytokines. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15672379
Volume :
53
Issue :
4
Database :
Complementary Index
Journal :
Journal of Molecular Histology
Publication Type :
Academic Journal
Accession number :
158509398
Full Text :
https://doi.org/10.1007/s10735-022-10085-7