Literature DB >> 18640065

Cell-based therapies for metabolic liver disease.

Gregory M Enns1, Maria T Millan.   

Abstract

Liver transplantation is an important therapeutic option for many individuals with metabolic liver disease. Nevertheless, the invasive nature of surgery and limitations of donor organ availability have led to the search for alternatives to whole-organ transplantation. Cell-based therapies have been a particularly active area of investigation in recent years. Hepatocyte transplantations have been performed for a variety of indications, including acute liver failure, end-stage liver disease, and inborn errors of metabolism. Individuals with inborn errors of metabolism who have undergone hepatocyte transplantation have shown clinical improvement and partial correction of the underlying metabolic defect. In most cases, sustained benefits have not been observed. This may be related to inadequate cell dose, variations in the quality of hepatocyte preparations, rejection of the transplanted cells, or senescence of transplanted hepatocytes. Though initial proof of concept with hepatocyte transplantation has been demonstrated by a number of investigators, wide application of this technology has been hindered by the inability to secure a reliable and well-characterized cell source(s) for transplantation and by the challenges of sustained engraftment and expansion of transplanted cells in vivo. Cell-based therapies, including those based on stem cells or more differentiated progenitor cells, may represent the future of cell transplantation for treatment of metabolic liver disease.

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Mesh:

Year:  2008        PMID: 18640065     DOI: 10.1016/j.ymgme.2008.06.001

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  22 in total

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Review 2.  The hematopoietic system in the context of regenerative medicine.

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3.  Human-induced pluripotent stem cells as a source of hepatocyte-like cells: new kids on the block.

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4.  Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells.

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Journal:  J Clin Invest       Date:  2010-08-25       Impact factor: 14.808

Review 5.  From skin cells to hepatocytes: advances in application of iPS cell technology.

Authors:  Linda E Greenbaum
Journal:  J Clin Invest       Date:  2010-08-25       Impact factor: 14.808

6.  Embryonic hepatocyte transplantation for hepatic cirrhosis: efficacy and mechanism of action.

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Journal:  World J Gastroenterol       Date:  2012-01-28       Impact factor: 5.742

Review 7.  Therapeutic liver repopulation for phenylketonuria.

Authors:  Cary O Harding; K M Gibson
Journal:  J Inherit Metab Dis       Date:  2010-05-22       Impact factor: 4.982

Review 8.  Mesenchymal stem cells as therapeutics and vehicles for gene and drug delivery.

Authors:  Christopher D Porada; Graça Almeida-Porada
Journal:  Adv Drug Deliv Rev       Date:  2010-09-07       Impact factor: 15.470

9.  Treatment of Hemophilia A in Utero and Postnatally using Sheep as a Model for Cell and Gene Delivery.

Authors:  Christopher D Porada; Graça Almeida-Porada
Journal:  J Genet Syndr Gene Ther       Date:  2012-05-25

10.  Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders.

Authors:  Jochen Meyburg; Thomas Opladen; Ute Spiekerkötter; Andrea Schlune; Jens-Peter Schenk; Jan Schmidt; Jürgen Weitz; Jürgen Okun; Friederike Bürger; Tawfeg Ben Omran; Ghassan Abdoh; Hilal Al Rifai; Ahmad Monavari; Vassiliki Konstantopoulou; Stefan Kölker; Marc Yudkoff; Georg F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2017-10-12       Impact factor: 4.982

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