Literature DB >> 18588477

Bioartificial liver systems: why, what, whither?

Jörg C Gerlach1, Katrin Zeilinger, John F Patzer Ii.   

Abstract

Acute liver disease is a life-threatening condition for which liver transplantation is the only recognized effective therapy. While etiology varies considerably, the clinical course of acute liver failure is common among the etiologies: encephalopathy progressing toward coma and multiple organ failure. Detoxification processes, such as molecular adsorbent recirculating system (MARS) and Prometheus, have had limited success in altering blood chemistries positively in clinical evaluations, but have not been shown to be clinically effective with regard to patient survival or other clinical outcomes in any Phase III prospective, randomized trial. Bioartificial liver systems, which use liver cells (hepatocytes) to provide metabolic support as well as detoxification, have shown promising results in early clinical evaluations, but again have not demonstrated clinical significance in any Phase III prospective, randomized trial. Cell transplantation therapy has had limited success but is not practicable for wide use owing to a lack of cells (whole-organ transplantation has priority). New approaches in regenerative medicine for treatment of liver disease need to be directed toward providing a functional cell source, expandable in large quantities, for use in various applications. To this end, a novel bioreactor design is described that closely mimics the native liver cell environment and is easily scaled from microscopic (<1 ml cells) to clinical ( approximately 600 ml cells) size, while maintaining the same local cell environment throughout the bioreactor. The bioreactor is used for study of primary liver cell isolates, liver-derived cell lines and stem/progenitor cells.

Entities:  

Mesh:

Year:  2008        PMID: 18588477     DOI: 10.2217/17460751.3.4.575

Source DB:  PubMed          Journal:  Regen Med        ISSN: 1746-0751            Impact factor:   3.806


  13 in total

Review 1.  Biology of the adult hepatic progenitor cell: "ghosts in the machine".

Authors:  Houda Darwiche; Bryon E Petersen
Journal:  Prog Mol Biol Transl Sci       Date:  2010       Impact factor: 3.622

2.  Functional ultrasound imaging for assessment of extracellular matrix scaffolds used for liver organoid formation.

Authors:  Ryan C Gessner; Ariel D Hanson; Steven Feingold; Avery T Cashion; Ana Corcimaru; Bryant T Wu; Christopher R Mullins; Stephen R Aylward; Lola M Reid; Paul A Dayton
Journal:  Biomaterials       Date:  2013-09-04       Impact factor: 12.479

3.  Cell therapeutic options in liver diseases: cell types, medical devices and regulatory issues.

Authors:  Andreas K Nussler; Katrin Zeilinger; Lilianna Schyschka; Sabrina Ehnert; Jörg C Gerlach; Xueying Yan; Serene M L Lee; Maren Ilowski; Wolfgang E Thasler; Thomas S Weiss
Journal:  J Mater Sci Mater Med       Date:  2011-04-03       Impact factor: 3.896

4.  Influence of chitosan nanofiber scaffold on porcine endogenous retroviral expression and infectivity in pig hepatocytes.

Authors:  Bing Han; Xiao-Lei Shi; Jiang-Qiang Xiao; Yue Zhang; Xue-Hui Chu; Jin-Yang Gu; Jia-Jun Tan; Zhong-Ze Gu; Yi-Tao Ding
Journal:  World J Gastroenterol       Date:  2011-06-14       Impact factor: 5.742

Review 5.  Bioreactor technologies to support liver function in vitro.

Authors:  Mohammad R Ebrahimkhani; Jaclyn A Shepard Neiman; Micha Sam B Raredon; David J Hughes; Linda G Griffith
Journal:  Adv Drug Deliv Rev       Date:  2014-03-05       Impact factor: 15.470

Review 6.  Bioartificial liver devices: Perspectives on the state of the art.

Authors:  Yi-Tao Ding; Xiao-Lei Shi
Journal:  Front Med       Date:  2010-11-19       Impact factor: 4.592

7.  Modulation of hepatocarcinoma cell morphology and activity by parylene-C coating on PDMS.

Authors:  Nazaré Pereira-Rodrigues; Paul-Emile Poleni; Denis Guimard; Yasuhiko Arakawa; Yasuyuki Sakai; Teruo Fujii
Journal:  PLoS One       Date:  2010-03-16       Impact factor: 3.240

8.  The nitric oxide donor S-nitrosoglutathione reduces apoptotic primary liver cell loss in a three-dimensional perfusion bioreactor culture model developed for liver support.

Authors:  Jose M Prince; Yoram Vodovotz; Matthew J Baun; Satdarshan Pal Monga; Timothy R Billiar; Jörg C Gerlach
Journal:  Tissue Eng Part A       Date:  2010-03       Impact factor: 3.845

Review 9.  Engineering liver.

Authors:  Linda G Griffith; Alan Wells; Donna B Stolz
Journal:  Hepatology       Date:  2014-05-19       Impact factor: 17.425

10.  Microbiological safety of a novel bio-artificial liver support system based on porcine hepatocytes: a experimental study.

Authors:  Bing Han; Xiao-Lei Shi; Yue Zhang; Xue-Hui Chu; Jin-Yang Gu; Jiang-Qiang Xiao; Hao-Zhen Ren; Jia-Jun Tan; Zhong-Ze Gu; Yi-Tao Ding
Journal:  Eur J Med Res       Date:  2012-05-25       Impact factor: 2.175

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