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Cell-based therapy in thin endometrium and Asherman syndrome
Numerous treatment strategies have so far been proposed for treating refractory thin endometrium either without or with the Asherman syndrome. Inconsistency in the improvement of endometrial thickness is a common limitation of such therapies including tamoxifen citrate as an ovulation induction agen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796444/ https://www.ncbi.nlm.nih.gov/pubmed/35090547 http://dx.doi.org/10.1186/s13287-021-02698-8 |
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author | Gharibeh, Nastaran Aghebati-Maleki, Leili Madani, Javad Pourakbari, Ramin Yousefi, Mehdi Ahmadian Heris, Javad |
author_facet | Gharibeh, Nastaran Aghebati-Maleki, Leili Madani, Javad Pourakbari, Ramin Yousefi, Mehdi Ahmadian Heris, Javad |
author_sort | Gharibeh, Nastaran |
collection | PubMed |
description | Numerous treatment strategies have so far been proposed for treating refractory thin endometrium either without or with the Asherman syndrome. Inconsistency in the improvement of endometrial thickness is a common limitation of such therapies including tamoxifen citrate as an ovulation induction agent, acupuncture, long-term pentoxifylline and tocopherol or tocopherol only, low-dose human chorionic gonadotropin during endometrial preparation, aspirin, luteal gonadotropin-releasing hormone agonist supplementation, and extended estrogen therapy. Recently, cell therapy has been proposed as an ideal alternative for endometrium regeneration, including the employment of stem cells, platelet-rich plasma, and growth factors as therapeutic agents. The mechanisms of action of cell therapy include the cytokine induction, growth factor production, natural killer cell activity reduction, Th17 and Th1 decrease, and Treg cell and Th2 increase. Since cell therapy is personalized, dynamic, interactive, and specific and could be an effective strategy. Despite its promising nature, further research is required for improving the procedure and the safety of this strategy. These methods and their results are discussed in this article. |
format | Online Article Text |
id | pubmed-8796444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87964442022-02-03 Cell-based therapy in thin endometrium and Asherman syndrome Gharibeh, Nastaran Aghebati-Maleki, Leili Madani, Javad Pourakbari, Ramin Yousefi, Mehdi Ahmadian Heris, Javad Stem Cell Res Ther Review Numerous treatment strategies have so far been proposed for treating refractory thin endometrium either without or with the Asherman syndrome. Inconsistency in the improvement of endometrial thickness is a common limitation of such therapies including tamoxifen citrate as an ovulation induction agent, acupuncture, long-term pentoxifylline and tocopherol or tocopherol only, low-dose human chorionic gonadotropin during endometrial preparation, aspirin, luteal gonadotropin-releasing hormone agonist supplementation, and extended estrogen therapy. Recently, cell therapy has been proposed as an ideal alternative for endometrium regeneration, including the employment of stem cells, platelet-rich plasma, and growth factors as therapeutic agents. The mechanisms of action of cell therapy include the cytokine induction, growth factor production, natural killer cell activity reduction, Th17 and Th1 decrease, and Treg cell and Th2 increase. Since cell therapy is personalized, dynamic, interactive, and specific and could be an effective strategy. Despite its promising nature, further research is required for improving the procedure and the safety of this strategy. These methods and their results are discussed in this article. BioMed Central 2022-01-28 /pmc/articles/PMC8796444/ /pubmed/35090547 http://dx.doi.org/10.1186/s13287-021-02698-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Gharibeh, Nastaran Aghebati-Maleki, Leili Madani, Javad Pourakbari, Ramin Yousefi, Mehdi Ahmadian Heris, Javad Cell-based therapy in thin endometrium and Asherman syndrome |
title | Cell-based therapy in thin endometrium and Asherman syndrome |
title_full | Cell-based therapy in thin endometrium and Asherman syndrome |
title_fullStr | Cell-based therapy in thin endometrium and Asherman syndrome |
title_full_unstemmed | Cell-based therapy in thin endometrium and Asherman syndrome |
title_short | Cell-based therapy in thin endometrium and Asherman syndrome |
title_sort | cell-based therapy in thin endometrium and asherman syndrome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796444/ https://www.ncbi.nlm.nih.gov/pubmed/35090547 http://dx.doi.org/10.1186/s13287-021-02698-8 |
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