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Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges
Autoimmune liver disease (AILD) is a series of chronic liver diseases with abnormal immune responses, including autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The treatment options for AILD remain limited, and the adverse side effects of the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887681/ https://www.ncbi.nlm.nih.gov/pubmed/33633826 http://dx.doi.org/10.1177/2040622321993442 |
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author | He, Chengmei Yang, Yanlei Zheng, Kunyu Chen, Yiran Liu, Suying Li, Yongzhe Han, Qin Zhao, Robert Chunhua Wang, Li Zhang, Fengchun |
author_facet | He, Chengmei Yang, Yanlei Zheng, Kunyu Chen, Yiran Liu, Suying Li, Yongzhe Han, Qin Zhao, Robert Chunhua Wang, Li Zhang, Fengchun |
author_sort | He, Chengmei |
collection | PubMed |
description | Autoimmune liver disease (AILD) is a series of chronic liver diseases with abnormal immune responses, including autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The treatment options for AILD remain limited, and the adverse side effects of the drugs that are typically used for treatment frequently lead to a low quality of life for AILD patients. Moreover, AILD patients may have a poor prognosis, especially those with an incomplete response to first-line treatment. Mesenchymal stem cells (MSCs) are pluripotent stem cells with low immunogenicity and can be conveniently harvested. MSC-based therapy is emerging as a promising approach for treating liver diseases based on their advantageous characteristics of immunomodulation, anti-fibrosis effects, and differentiation to hepatocytes, and accumulating evidence has revealed the positive effects of MSC therapy in AILD. In this review, we first summarize the mechanisms, safety, and efficacy of MSC treatment for AILD based on work in animal and clinical studies. We also discuss the challenges of MSC therapy in clinical applications. In summary, although promising data from preclinical studies are now available, MSC therapy is currently far for being applied in clinical practice, thus developing MSC therapy in AILD is still challenging and warrants further research. |
format | Online Article Text |
id | pubmed-7887681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78876812021-02-24 Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges He, Chengmei Yang, Yanlei Zheng, Kunyu Chen, Yiran Liu, Suying Li, Yongzhe Han, Qin Zhao, Robert Chunhua Wang, Li Zhang, Fengchun Ther Adv Chronic Dis Review Autoimmune liver disease (AILD) is a series of chronic liver diseases with abnormal immune responses, including autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The treatment options for AILD remain limited, and the adverse side effects of the drugs that are typically used for treatment frequently lead to a low quality of life for AILD patients. Moreover, AILD patients may have a poor prognosis, especially those with an incomplete response to first-line treatment. Mesenchymal stem cells (MSCs) are pluripotent stem cells with low immunogenicity and can be conveniently harvested. MSC-based therapy is emerging as a promising approach for treating liver diseases based on their advantageous characteristics of immunomodulation, anti-fibrosis effects, and differentiation to hepatocytes, and accumulating evidence has revealed the positive effects of MSC therapy in AILD. In this review, we first summarize the mechanisms, safety, and efficacy of MSC treatment for AILD based on work in animal and clinical studies. We also discuss the challenges of MSC therapy in clinical applications. In summary, although promising data from preclinical studies are now available, MSC therapy is currently far for being applied in clinical practice, thus developing MSC therapy in AILD is still challenging and warrants further research. SAGE Publications 2021-02-12 /pmc/articles/PMC7887681/ /pubmed/33633826 http://dx.doi.org/10.1177/2040622321993442 Text en © The Author(s), 2021 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 | Review He, Chengmei Yang, Yanlei Zheng, Kunyu Chen, Yiran Liu, Suying Li, Yongzhe Han, Qin Zhao, Robert Chunhua Wang, Li Zhang, Fengchun Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title | Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title_full | Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title_fullStr | Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title_full_unstemmed | Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title_short | Mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
title_sort | mesenchymal stem cell-based treatment in autoimmune liver diseases: underlying roles, advantages and challenges |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7887681/ https://www.ncbi.nlm.nih.gov/pubmed/33633826 http://dx.doi.org/10.1177/2040622321993442 |
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