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      Cell-based therapy in thin endometrium and Asherman syndrome

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          Abstract

          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.

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          Most cited references108

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          PCNA, the maestro of the replication fork.

          Inheritance requires genome duplication, reproduction of chromatin and its epigenetic information, mechanisms to ensure genome integrity, and faithful transmission of the information to progeny. Proliferating cell nuclear antigen (PCNA)-a cofactor of DNA polymerases that encircles DNA-orchestrates several of these functions by recruiting crucial players to the replication fork. Remarkably, many factors that are involved in replication-linked processes interact with a particular face of PCNA and through the same interaction domain, indicating that these interactions do not occur simultaneously during replication. Switching of PCNA partners may be triggered by affinity-driven competition, phosphorylation, proteolysis, and modification of PCNA by ubiquitin and SUMO.
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            Platelet-rich plasma: evidence to support its use.

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              Mesenchymal stem cells and immunomodulation: current status and future prospects

              The unique immunomodulatory properties of mesenchymal stem cells (MSCs) make them an invaluable cell type for the repair of tissue/ organ damage caused by chronic inflammation or autoimmune disorders. Although they hold great promise in the treatment of immune disorders such as graft versus host disease (GvHD) and allergic disorders, there remain many challenges to overcome before their widespread clinical application. An understanding of the biological properties of MSCs will clarify the mechanisms of MSC-based transplantation for immunomodulation. In this review, we summarize the preclinical and clinical studies of MSCs from different adult tissues, discuss the current hurdles to their use and propose the future development of pluripotent stem cell-derived MSCs as an approach to immunomodulation therapy.
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                Author and article information

                Contributors
                Yousefime@tbzmed.ac.ir
                jahmadian@yahoo.com
                Journal
                Stem Cell Res Ther
                Stem Cell Res Ther
                Stem Cell Research & Therapy
                BioMed Central (London )
                1757-6512
                28 January 2022
                28 January 2022
                2022
                : 13
                : 33
                Affiliations
                [1 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Student’s Research Committee, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                [2 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Stem Cell Research Center, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                [3 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Immunology Research Center, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                [4 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Department of Allergy and Clinical Immunology, Pediatric Hospital, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                [5 ]GRID grid.412888.f, ISNI 0000 0001 2174 8913, Department of Immunology, School of Medicine, , Tabriz University of Medical Sciences, ; Tabriz, Iran
                Article
                2698
                10.1186/s13287-021-02698-8
                8796444
                35090547
                704e4407-d8d8-4522-9298-f2ebc55f6123
                © The Author(s) 2022

                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/. The Creative Commons Public Domain Dedication waiver ( http://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.

                History
                : 8 June 2021
                : 24 December 2021
                Categories
                Review
                Custom metadata
                © The Author(s) 2022

                Molecular medicine
                cell therapy,endometrium,asherman syndrome
                Molecular medicine
                cell therapy, endometrium, asherman syndrome

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