Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gharibeh, Nastaran, Aghebati-Maleki, Leili, Madani, Javad, Pourakbari, Ramin, Yousefi, Mehdi, Ahmadian Heris, Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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
_version_ 1784641329111760896
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
work_keys_str_mv AT gharibehnastaran cellbasedtherapyinthinendometriumandashermansyndrome
AT aghebatimalekileili cellbasedtherapyinthinendometriumandashermansyndrome
AT madanijavad cellbasedtherapyinthinendometriumandashermansyndrome
AT pourakbariramin cellbasedtherapyinthinendometriumandashermansyndrome
AT yousefimehdi cellbasedtherapyinthinendometriumandashermansyndrome
AT ahmadianherisjavad cellbasedtherapyinthinendometriumandashermansyndrome