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Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial

Currently, the only effective therapy for cirrhosis of the liver is liver transplantation. However, finding a compatible liver is difficult due to the low supply of healthy livers and the ever-increasing demand. However, stem-cell therapy may offer a solution for liver cirrhosis; for example, GXHPC1...

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Autores principales: Huang, Ko-Chang, Chuang, Ming-Hsi, Lin, Zung-Sheng, Lin, Yi-Chun, Chen, Chun-Hung, Chang, Chao-Liang, Huang, Pi-Chun, Syu, Wan-Sin, Chiou, Tzyy-Wen, Hong, Zih-Han, Tsai, Yu-Chen, Harn, Horng-Jyh, Lin, Po-Cheng, Lin, Shinn-Zong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016466/
https://www.ncbi.nlm.nih.gov/pubmed/31722556
http://dx.doi.org/10.1177/0963689719884885
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author Huang, Ko-Chang
Chuang, Ming-Hsi
Lin, Zung-Sheng
Lin, Yi-Chun
Chen, Chun-Hung
Chang, Chao-Liang
Huang, Pi-Chun
Syu, Wan-Sin
Chiou, Tzyy-Wen
Hong, Zih-Han
Tsai, Yu-Chen
Harn, Horng-Jyh
Lin, Po-Cheng
Lin, Shinn-Zong
author_facet Huang, Ko-Chang
Chuang, Ming-Hsi
Lin, Zung-Sheng
Lin, Yi-Chun
Chen, Chun-Hung
Chang, Chao-Liang
Huang, Pi-Chun
Syu, Wan-Sin
Chiou, Tzyy-Wen
Hong, Zih-Han
Tsai, Yu-Chen
Harn, Horng-Jyh
Lin, Po-Cheng
Lin, Shinn-Zong
author_sort Huang, Ko-Chang
collection PubMed
description Currently, the only effective therapy for cirrhosis of the liver is liver transplantation. However, finding a compatible liver is difficult due to the low supply of healthy livers and the ever-increasing demand. However, stem-cell therapy may offer a solution for liver cirrhosis; for example, GXHPC1 therapy preparation contains adipose-derived mesenchymal stem cells (AD-MSCs) and was developed for the treatment of liver cirrhosis. In our previous report, animal studies suggested that treatment of a diseased liver via GXHPC1 transplantation can abrogate liver fibrosis and facilitate recovery of liver function. In our current human trial, patients with liver cirrhosis were included. Their adipose tissue was harvested from the subcutaneous fat of the abdominal wall during surgery. AD-MSCs were cultured and suspended at a concentration of 100 million cells in 1 ml of physiological saline (i.e., GXHPC1). This human study passed the Taiwan Food and Drug Administration IND inspection and received Phase I clinical trial permission. The trial was conducted with six patients with liver cirrhosis to demonstrate the safety and efficacy of administering GXHPC1. Intrahepatic injection of GXHPC1 did not cause any safety issues in the analysis of adverse drug reactions and suspected unexpected serious adverse reactions, and showed a tendency for improvement of liver function, METAVIR score, Child–Pugh score, MELD score, and quality of life for patients with liver cirrhosis.
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spelling pubmed-70164662020-02-27 Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial Huang, Ko-Chang Chuang, Ming-Hsi Lin, Zung-Sheng Lin, Yi-Chun Chen, Chun-Hung Chang, Chao-Liang Huang, Pi-Chun Syu, Wan-Sin Chiou, Tzyy-Wen Hong, Zih-Han Tsai, Yu-Chen Harn, Horng-Jyh Lin, Po-Cheng Lin, Shinn-Zong Cell Transplant Original Articles Currently, the only effective therapy for cirrhosis of the liver is liver transplantation. However, finding a compatible liver is difficult due to the low supply of healthy livers and the ever-increasing demand. However, stem-cell therapy may offer a solution for liver cirrhosis; for example, GXHPC1 therapy preparation contains adipose-derived mesenchymal stem cells (AD-MSCs) and was developed for the treatment of liver cirrhosis. In our previous report, animal studies suggested that treatment of a diseased liver via GXHPC1 transplantation can abrogate liver fibrosis and facilitate recovery of liver function. In our current human trial, patients with liver cirrhosis were included. Their adipose tissue was harvested from the subcutaneous fat of the abdominal wall during surgery. AD-MSCs were cultured and suspended at a concentration of 100 million cells in 1 ml of physiological saline (i.e., GXHPC1). This human study passed the Taiwan Food and Drug Administration IND inspection and received Phase I clinical trial permission. The trial was conducted with six patients with liver cirrhosis to demonstrate the safety and efficacy of administering GXHPC1. Intrahepatic injection of GXHPC1 did not cause any safety issues in the analysis of adverse drug reactions and suspected unexpected serious adverse reactions, and showed a tendency for improvement of liver function, METAVIR score, Child–Pugh score, MELD score, and quality of life for patients with liver cirrhosis. SAGE Publications 2019-11-14 2019-12 /pmc/articles/PMC7016466/ /pubmed/31722556 http://dx.doi.org/10.1177/0963689719884885 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Huang, Ko-Chang
Chuang, Ming-Hsi
Lin, Zung-Sheng
Lin, Yi-Chun
Chen, Chun-Hung
Chang, Chao-Liang
Huang, Pi-Chun
Syu, Wan-Sin
Chiou, Tzyy-Wen
Hong, Zih-Han
Tsai, Yu-Chen
Harn, Horng-Jyh
Lin, Po-Cheng
Lin, Shinn-Zong
Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title_full Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title_fullStr Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title_full_unstemmed Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title_short Transplantation with GXHPC1 for Liver Cirrhosis: Phase 1 Trial
title_sort transplantation with gxhpc1 for liver cirrhosis: phase 1 trial
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016466/
https://www.ncbi.nlm.nih.gov/pubmed/31722556
http://dx.doi.org/10.1177/0963689719884885
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