Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis

Primary biliary cholangitis (PBC) is a chronic autoimmune cholestatic liver disease characterized by the progressive destruction of small- and medium-sized intrahepatic bile ducts with resultant cholestasis and progressive fibrosis. Ursodeoxycholic acid and obethicholic acid are the only agents appr...

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Main Authors: Aleksandar Arsenijevic, C. Randall Harrell, Crissy Fellabaum, Vladislav Volarevic
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2017/7492836
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author Aleksandar Arsenijevic
C. Randall Harrell
Crissy Fellabaum
Vladislav Volarevic
author_facet Aleksandar Arsenijevic
C. Randall Harrell
Crissy Fellabaum
Vladislav Volarevic
author_sort Aleksandar Arsenijevic
collection DOAJ
description Primary biliary cholangitis (PBC) is a chronic autoimmune cholestatic liver disease characterized by the progressive destruction of small- and medium-sized intrahepatic bile ducts with resultant cholestasis and progressive fibrosis. Ursodeoxycholic acid and obethicholic acid are the only agents approved by the US Food and Drug Administration (FDA) for the treatment of PBC. However, for patients with advanced, end-stage PBC, liver transplantation is still the most effective treatment. Accordingly, the alternative approaches, such as mesenchymal stem cell (MSC) transplantation, have been suggested as an effective alternative therapy for these patients. Due to their immunomodulatory characteristics, MSCs are considered as promising therapeutic agents for the therapy of autoimmune liver diseases, including PBC. In this review, we have summarized the therapeutic potential of MSCs for the treatment of these diseases, emphasizing molecular and cellular mechanisms responsible for MSC-based effects in an animal model of PBC and therapeutic potential observed in recently conducted clinical trials. We have also presented several outstanding problems including safety issues regarding unwanted differentiation of transplanted MSCs which limit their therapeutic use. Efficient and safe MSC-based therapy for PBC remains a challenging issue that requires continuous cooperation between clinicians, researchers, and patients.
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series Analytical Cellular Pathology
spelling doaj-art-66974873262e4a18b3ad2fce4dee83fe2025-02-03T06:06:40ZengWileyAnalytical Cellular Pathology2210-71772210-71852017-01-01201710.1155/2017/74928367492836Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary CholangitisAleksandar Arsenijevic0C. Randall Harrell1Crissy Fellabaum2Vladislav Volarevic3Faculty of Medical Sciences, Department of Microbiology and Immunology, Center for Molecular Medicine and Stem Cell Research, University of Kragujevac, Kragujevac, SerbiaRegenerative Processing Plant, LLC, Palm Harbor, FL, USARegenerative Processing Plant, LLC, Palm Harbor, FL, USAFaculty of Medical Sciences, Department of Microbiology and Immunology, Center for Molecular Medicine and Stem Cell Research, University of Kragujevac, Kragujevac, SerbiaPrimary biliary cholangitis (PBC) is a chronic autoimmune cholestatic liver disease characterized by the progressive destruction of small- and medium-sized intrahepatic bile ducts with resultant cholestasis and progressive fibrosis. Ursodeoxycholic acid and obethicholic acid are the only agents approved by the US Food and Drug Administration (FDA) for the treatment of PBC. However, for patients with advanced, end-stage PBC, liver transplantation is still the most effective treatment. Accordingly, the alternative approaches, such as mesenchymal stem cell (MSC) transplantation, have been suggested as an effective alternative therapy for these patients. Due to their immunomodulatory characteristics, MSCs are considered as promising therapeutic agents for the therapy of autoimmune liver diseases, including PBC. In this review, we have summarized the therapeutic potential of MSCs for the treatment of these diseases, emphasizing molecular and cellular mechanisms responsible for MSC-based effects in an animal model of PBC and therapeutic potential observed in recently conducted clinical trials. We have also presented several outstanding problems including safety issues regarding unwanted differentiation of transplanted MSCs which limit their therapeutic use. Efficient and safe MSC-based therapy for PBC remains a challenging issue that requires continuous cooperation between clinicians, researchers, and patients.http://dx.doi.org/10.1155/2017/7492836
spellingShingle Aleksandar Arsenijevic
C. Randall Harrell
Crissy Fellabaum
Vladislav Volarevic
Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
Analytical Cellular Pathology
title Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
title_full Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
title_fullStr Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
title_full_unstemmed Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
title_short Mesenchymal Stem Cells as New Therapeutic Agents for the Treatment of Primary Biliary Cholangitis
title_sort mesenchymal stem cells as new therapeutic agents for the treatment of primary biliary cholangitis
url http://dx.doi.org/10.1155/2017/7492836
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AT crandallharrell mesenchymalstemcellsasnewtherapeuticagentsforthetreatmentofprimarybiliarycholangitis
AT crissyfellabaum mesenchymalstemcellsasnewtherapeuticagentsforthetreatmentofprimarybiliarycholangitis
AT vladislavvolarevic mesenchymalstemcellsasnewtherapeuticagentsforthetreatmentofprimarybiliarycholangitis