<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBM</journal-id><journal-title-group><journal-title>Journal of Biosciences and Medicines</journal-title></journal-title-group><issn pub-type="epub">2327-5081</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbm.2021.91009</article-id><article-id pub-id-type="publisher-id">JBM-106827</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Intrauterine Adhesions (IUAs) or Asherman’s Syndrome (AS) and the Stem Cells Treatment: A Systemic Review and Meta-Analysis
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sichen</surname><given-names>Zhang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ying</surname><given-names>Mao</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Xiaodong</surname><given-names>Zhao</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Huiwen</surname><given-names>Zhang</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Xingbo</surname><given-names>Long</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shaowei</surname><given-names>Wang</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Min</surname><given-names>Ma</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Peking Union Medical College, Chinese Academy of Medical Sciences, Santiao, Beijing, China</addr-line></aff><aff id="aff3"><addr-line>National Cancer Center/Cancer Hospital, Beijing, China</addr-line></aff><aff id="aff1"><addr-line>Department of Gynecology and Obstetrics, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, China</addr-line></aff><pub-date pub-type="epub"><day>11</day><month>01</month><year>2021</year></pub-date><volume>09</volume><issue>01</issue><fpage>105</fpage><lpage>118</lpage><history><date date-type="received"><day>30,</day>	<month>December</month>	<year>2020</year></date><date date-type="rev-recd"><day>25,</day>	<month>January</month>	<year>2021</year>	</date><date date-type="accepted"><day>28,</day>	<month>January</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Intrauterine Adhesions (IUAs) or Asherman’s Syndrome (AS) usually contains symptoms such as decreased menstrual flow or even amenorrhea, chronic pelvic pain, recurrent abortion and infertility. The current treatment of IUAs includes hysteroscopic adhesiolysis, oral hormone and biological barriers, but each of them has limitation. Stem cell therapy may be an expanding field seeking for therapy in IUAs. 
  Objective: We will discuss current advances in stem cell therapy as a treatment for endometrial pathophysiology. 
  Materials and Methods: We search on PubMed, Embase and Cochrane library and select several keywords on researches, then review the cell biology theories and animal experiments, finally do meta-analysis in human clinical trials. 
  Results: 77 articles on PubMed, 71 articles on Embase and 17 articles on Cochrane Library, as a result, 37 articles are included under the criteria, which are intrauterine adhesions (IUAs), Asherman’s Syndrome (AS), cell therapy, stem cells, bone marrow stem cells, clinical trials, recent 10 years and human or animal experiments. The included criteria: original articles, cohort study, case control study, animal experiments, human clinical trials, high quality, 10 years recent. The excluded articles are case reports, meeting reports, low quality or more than 10 years ago. 
  Conclusion: Stem cell may be a new therapeutic schedule for IUAs in the future clinical treatment, but it is necessary to compare it with traditional therapy such as oral hormone, also the development of random clinical tests should proceed. For clinical treatment on IUAs, stem cells could be a new choice.
 
</p></abstract><kwd-group><kwd>Intrauterine Adhesions IUA</kwd><kwd> Asherman’s Syndrome</kwd><kwd> Stem Cells</kwd><kwd> Therapy</kwd><kwd> Infertility</kwd><kwd> Meta-Analysis</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Intrauterine Adhesions (IUAs) or Asherman’s Syndrome (AS) is common caused by inflammatory or trauma damaging the endometrial basal layer after delivery or surgery [<xref ref-type="bibr" rid="scirp.106827-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref3">3</xref>]. The epidemiology of IUAs is unclear now, however, some researchers have reported that approximately 19% amongst women suffering miscarriage and being prospectively assessed by hysteroscopy within 1 year [<xref ref-type="bibr" rid="scirp.106827-ref4">4</xref>]. In addition, about 70% of patients with severe Asherman’s Syndrome had history of instrumentation such as aspirator during the postpartum period [<xref ref-type="bibr" rid="scirp.106827-ref5">5</xref>], whereas approximately 80% - 90% patients with mild Asherman’s Syndrome had similar procedures experienced at the first trimester. Furthermore, amongst women surgically treated for retained products of conception and evaluated hysteroscopy afterwards, the overall incidence of IUAs varies widely between 6 and 22% [<xref ref-type="bibr" rid="scirp.106827-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref7">7</xref>].</p><p>The typical symptoms of IUAs or AS include decreased menstrual flow or amenorrhea, chronic pelvic pain, recurrent abortion and infertility [<xref ref-type="bibr" rid="scirp.106827-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref9">9</xref>]. However, the exact pathophysiologic origin of IUAs is still unclear. With expanded clinical awareness and availability of diagnostic testing, the frequency of diagnosis of IUAs has increased. Generally, the diagnosis of intrauterine adhesions depends on symptoms like menstruation and fertility and test such as ultrasound, Magnetic Resonance Imaging (MRI), Hysterosalpingography (HSG) and hysteroscopy [<xref ref-type="bibr" rid="scirp.106827-ref3">3</xref>]. Under a few of decades exploring and practice, the clinician recommended hysteroscopy as the golden standard of diagnosis by following the European Society of Gynecological Endoscopy (ESGE) publish the guidelines of diagnosis in 2016 [<xref ref-type="bibr" rid="scirp.106827-ref4">4</xref>].</p><p>In addition, the classification of IUAs is various in different areas, but no one is accepted universally, however, each of them is based on the grade of European Society for Hysteroscopy (ESH) in 1989 [<xref ref-type="bibr" rid="scirp.106827-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref9">9</xref>] and American Fertility Society (AFS) in 1988 [<xref ref-type="bibr" rid="scirp.106827-ref1">1</xref>].</p><p>Currently, the therapeutic methods of IUAs include hysteroscopic adhesiolysis, oral hormone and biological barriers [<xref ref-type="bibr" rid="scirp.106827-ref10">10</xref>]. Primarily, severe forms may require multiple hysteroscopic adhesiolysis to achieve a satisfactory anatomical and functional result. Unfortunately, the recurrent rate of IUAs after hysteroscopy therapy is high [<xref ref-type="bibr" rid="scirp.106827-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref10">10</xref>]. Then, estrogen supplementation is commonly given postoperatively to stimulate endometrial growth; yet, there is no standard dosage length or regimen or explanation of risk of stimulating breast and ovarian tumor [<xref ref-type="bibr" rid="scirp.106827-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref12">12</xref>]. At last, using intrauterine barriers such as balloons, catheters and other intrauterine devices which may keep the uterine walls apart from adhesiolysis to reduce adhesion recurrence are frequently employed [<xref ref-type="bibr" rid="scirp.106827-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref14">14</xref>]. Whereas, 2010 American Association of Gynecologic Laparoscopists (AAGL) Practice Guidelines do not support use of antibiotic therapy before, during or after surgical management of IUAs because of increasing risks of infection [<xref ref-type="bibr" rid="scirp.106827-ref4">4</xref>].</p><p>In recent year, stem cell therapy [<xref ref-type="bibr" rid="scirp.106827-ref15">15</xref>] is an expanding field that seeks for alleviating numerous diseases involving malignant tumor, fibrosis, wound repair and inflammation. In addition, currently, cell bio-therapeutics for AS employ numerous sources of stromal and hematopoietic cell populations, including menstrual blood derived stromal cells (MenSCs), Umbilical Cord (UC) derived Mesenchymal Stromal Cells (MSCs), Bone Marrow derived Mononuclear Cells (BMMNCs) and peripheral blood derived mobilized populations. Thus, we aim to conclude stem cell therapy and IUAs or AS association in animal models and human clinical trials [<xref ref-type="bibr" rid="scirp.106827-ref16">16</xref>]. However, the problems of stem cells therapy like ethic, immune reaction or even risks of tumorigenesis limit it application in clinic, also, unknown mechanism, like gene regulation, protein modulation or paracrine effects should be explored and confirmed by future and it can be a new irritation for researchers.</p><p>In this article, we will discuss current advances in stem cell therapy as a treatment for intrauterine adhesions (IUAs) or Asherman’s Syndrome (AS).</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>We search on PubMed, Embase and Cochrane library and select several keywords on researches including: intrauterine adhesions (IUAs), Asherman’s Syndrome (AS), cell therapy, stem cells, bone marrow stem cells, clinical trials, recent 10 years and human or animal experiments. The included criteria: original articles, cohort study, case control study, animal experiments, human clinical trials, high quality, 10 years recent. In addition, the excluded criteria: case reports, meeting reports, low quality, more than 10 years ago.</p><p>Each article abstraction was performed using a standardized form; which included study characteristics such as year, author, area, type of study. Also each study should be scored under the scoring system like NOS (Newcastle-Ottawa quality assessment scale), Jadad, CASPin and iCAHE.</p><p>All the researches on human clinical trials are single-arm trials, and the data are extracted from text, tables, or figures. We conclude them and do the meta-analysis, all the differences in continuous outcomes using mean, weight mean difference (WMD) and sample size for each group, meanwhile Binary outcome is expressed as Odds Ratio (OR) and 95% Confidence Interval (CI). Hozo formula was used to convert data expressed as median and range. Statistical analysis was performed using Meta-Analyst.</p></sec><sec id="s3"><title>3. Results</title><p>Depending on those search strategies, we found about 77 articles on PubMed, 71 articles on Embase and 17 articles on Cochrane Library. As a result, 37 articles are included under the criteria, which are in details: clinical treatment 4, molecular 8, guideline 3, review article 7, stem cells application 15 (animal 10, human 5). The search process is below as the <xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="table" rid="table1">Table 1</xref> illustrates the scores and quality of the articles.</p><sec id="s3_1"><title>3.1. Molecular Experiments for Stem Cell and IUAs</title><p>Multiple studies show that the stem cells may improve the outcomes of injuring diseases [<xref ref-type="bibr" rid="scirp.106827-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref18">18</xref>], but it is still unclear that whether stem cells transplantation can be used as a therapy for IUAs. Nesrine [<xref ref-type="bibr" rid="scirp.106827-ref19">19</xref>] et al. Investigated the Transforming Growth Factors-β (TGF-β), Tumor Necrosis Factor-α (TNF-α) and Vascular Endothelial Growth Factor (VEGF) are significant decreased in extracellular vesicles derived from human umbilical cord mesenchymal stem cells (UCMSCs-EVs) alone or combined with estrogen therapeutic groups. Also, they reported that mesenchymal stem cells (MSCs) play a significant role in repairing injured tissues, which through the secretion of a wide range of paracrine factors. In addition, bone marrow stem cells (BMSCs) have been hypothesized to be important for endometrial regeneration and repair. In addition, a great deal of studies reported that endometrial stem cells could contribute to endometrial repairing physiologically, which may be crucial for the treatment of IUAs. An increasing number of evidences have proposed that stem cells play a key role in developing the therapeutic strategies for IUAs, although the molecular mechanism has not been acknowledged.</p><p>Recently, some researchers [<xref ref-type="bibr" rid="scirp.106827-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref21">21</xref>] devote to explore the hypothesis and evidence of stem cells repairing in IUAs. Typically, Estrogen Receptor α (ERα) is able to effectively promote BMSC proliferation and migration via Stromal Derived Factor/Chemokine Receptor type 4 (SDF-1/CXCR-4) according to Zhou et al. [<xref ref-type="bibr" rid="scirp.106827-ref22">22</xref>]. They point out that the upregulation of anti-inflammatory cytokines (base Fibroblast Growth Factor, bFGF and Interleukin, IL6) and the droppedregulation of pro-inflammatory cytokines after BMSCs transplantation may stimulate proliferation endometrial cell and exert an inhibitory action on endometrial</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Summary of researches</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle" >No.</th><th align="center" valign="middle" >Title</th><th align="center" valign="middle" >Author</th><th align="center" valign="middle" >Year</th><th align="center" valign="middle" >Type</th><th align="center" valign="middle" >Tools</th><th align="center" valign="middle" >Scores</th><th align="center" valign="middle" >Quality</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >Effectiveness of estrogen treatment before transcervical resection of adhesions on moderate and severe uterine adhesion patients</td><td align="center" valign="middle" >Ai-Zhen Liu</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >case-cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >Prevalence of intrauterine adhesions after the application of hyaluronic acid gel after dilatation and curettage in women with at least one previous curettage: short-term outcomes of a multicenter, prospective randomized controlled trial</td><td align="center" valign="middle" >Angelo B. Hooker, M.D</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >RCT</td><td align="center" valign="middle" >Jadad</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >The incidence of post-operative adhesion following transection of uterine septum: a cohort study comparing three different adjuvant therapies</td><td align="center" valign="middle" >Xiao Yu</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >The management of Asherman syndrome: a review of literature</td><td align="center" valign="middle" >Alessandro Conforti</td><td align="center" valign="middle" >2013</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >Transdermal estrogen gel and oral aspirin combination therapy improves fertility prognosis via the promotion of endometrial receptivity in moderate to severe intrauterine adhesion</td><td align="center" valign="middle" >Yuguang Chi</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >RCT</td><td align="center" valign="middle" >Jadad</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >AAGL Practice Report: Practice Guidelines for Management of Intrauterine Synechiae</td><td align="center" valign="middle" >AAGL</td><td align="center" valign="middle" >2009</td><td align="center" valign="middle" >clinical practical guideline</td><td align="center" valign="middle" >iCAHE guideline quality checklist</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >AAGL Practice Report: Practice Guidelines on Intrauterine Adhesions Developed in Collaboration With the European Society of Gynaecological Endoscopy (ESGE)</td><td align="center" valign="middle" >AAGL</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >clinical practical guideline</td><td align="center" valign="middle" >iCAHE guideline quality checklist</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >Review of Intrauterine Adhesions</td><td align="center" valign="middle" >Rebecca Deans</td><td align="center" valign="middle" >2010</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >9</td><td align="center" valign="middle" >Abnormal expression of fibrosis markers, estrogen receptor α and stromal derived factor-1/chemokine (C-X-C motif) receptor-4 axis in intrauterine adhesions</td><td align="center" valign="middle" >QIN ZHOU</td><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >basic research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >Elevated NF-κB signaling in Asherman syndrome patients and animal models</td><td align="center" valign="middle" >Xiangzhen Wang</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >basic research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >11</td><td align="center" valign="middle" >Molecular implication of ADAM-15 and 17 in intrauterine adhesions</td><td align="center" valign="middle" >Dan Liu</td><td align="center" valign="middle" >2013</td><td align="center" valign="middle" >basic research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >12</td><td align="center" valign="middle" >Role of Transforming Growth Factor-β1 and Smads Signaling Pathway in Intrauterine Adhesion</td><td align="center" valign="middle" >Umme Salma</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >basicl research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >13</td><td align="center" valign="middle" >The Overexpression of TGF-β and CCN2 in Intrauterine Adhesions Involves the NF-κB Signaling Pathway</td><td align="center" valign="middle" >Xiang Xue</td><td align="center" valign="middle" >2015</td><td align="center" valign="middle" >basicl research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle" >14</th><th align="center" valign="middle" >The expression of marker for endometrial stem cell and fibrosis was increased in intrauterine adhesious</th><th align="center" valign="middle" >Jianguo Hu</th><th align="center" valign="middle" >2015</th><th align="center" valign="middle" >basic research</th><th align="center" valign="middle" >ARRIVE</th><th align="center" valign="middle" >17</th><th align="center" valign="middle" >high</th></tr></thead><tr><td align="center" valign="middle" >15</td><td align="center" valign="middle" >A 10-year Review of the Clinical Presentation and Treatment Outcome of Asherman’s Syndrome at a Center with Limited Resources</td><td align="center" valign="middle" >IU Takai</td><td align="center" valign="middle" >2015</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >16</td><td align="center" valign="middle" >Systemic administration of bone marrow-derived cells leads to better uterine engraftment than use of uterine-derived cells or local injection</td><td align="center" valign="middle" >Ying Liu</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >17</td><td align="center" valign="middle" >A comprehensive review of Asherman’s syndrome: causes, symptoms and treatment options</td><td align="center" valign="middle" >Christina A. Salazar</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >18</td><td align="center" valign="middle" >Cellular therapies for the endometrium</td><td align="center" valign="middle" >Suzanna Queckbörner</td><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >19</td><td align="center" valign="middle" >Efficacy and Safety of Hyaluronic Acid Gel for the Prevention of Intrauterine Adhesion: A Meta-Analysis of Randomized Clinical Trials</td><td align="center" valign="middle" >Huafang Liu</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >Intrauterine adhesion prevention after hysteroscopy: a systematic review and meta-analysis</td><td align="center" valign="middle" >Mae Wu Healy</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >21</td><td align="center" valign="middle" >Meta-analysis of the use of amniotic membrane to prevent recurrence of intrauterine adhesion after hysteroscopic adhesiolysis</td><td align="center" valign="middle" >Fei Zheng</td><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >22</td><td align="center" valign="middle" >Endometrial reconstruction from stem cells</td><td align="center" valign="middle" >Caroline E. Gargett, Ph.D</td><td align="center" valign="middle" >2012</td><td align="center" valign="middle" >review</td><td align="center" valign="middle" >CASPin</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >23</td><td align="center" valign="middle" >CXCL12 Promotes Stem Cell Recruitment and Uterine Repair after Injury in Asherman’s Syndrome</td><td align="center" valign="middle" >Gulcin Sahin Ersoy</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >24</td><td align="center" valign="middle" >Application of Bone Marrow-Derived Mesenchymal Stem Cells in the Treatment of Intrauterine Adhesions in Rats</td><td align="center" valign="middle" >Jianmei Wang</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >25</td><td align="center" valign="middle" >Feasibility analysis of treating severe intrauterine adhesions by transplanting menstrual blood-derived stem cells</td><td align="center" valign="middle" >SHEN-XIA ZHENG</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >26</td><td align="center" valign="middle" >Human amniotic mesenchymal stromal cell transplantation improves endometrial regeneration in rodent models of intrauterine adhesions</td><td align="center" valign="middle" >LU GAN</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >27</td><td align="center" valign="middle" >Human mesenchymal stem cell-derived extracellular vesicles/estrogen combined therapy safely ameliorates experimentally induced intrauterine adhesions in a female rat model</td><td align="center" valign="middle" >Nesrine Ebrahim</td><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr></tbody></table></table-wrap><table-wrap id="1_3"><table><tbody><thead><tr><th align="center" valign="middle" >28</th><th align="center" valign="middle" >Neupogen and mesenchymal stem cells are the novel therapeutic agents in regeneration of induced endometrial fibrosis in experimental rats</th><th align="center" valign="middle" >Dina Sabry</th><th align="center" valign="middle" >2017</th><th align="center" valign="middle" >animal research</th><th align="center" valign="middle" >ARRIVE</th><th align="center" valign="middle" >16</th><th align="center" valign="middle" >moderate</th></tr></thead><tr><td align="center" valign="middle" >29</td><td align="center" valign="middle" >Vitamin C plus hydrogel facilitates bone marrow stromal cell-mediated endometrium regeneration in rats</td><td align="center" valign="middle" >Huan Yang</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >30</td><td align="center" valign="middle" >Bone Marrow-Derived Stem Cell (BMDSC) Transplantation Improves Fertility in a Murine Model of Asherman’s Syndrome</td><td align="center" valign="middle" >Feryal Alawadhi</td><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >31</td><td align="center" valign="middle" >Effect of stem cell application on Asherman syndrome, an experimental rat model</td><td align="center" valign="middle" >Sevtap Kilic</td><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >32</td><td align="center" valign="middle" >Platelet-rich plasma improves therapeutic effects of menstrual blood-derived stromal cells in rat model of intrauterine adhesion</td><td align="center" valign="middle" >Siwen Zhang</td><td align="center" valign="middle" >2019</td><td align="center" valign="middle" >animal research</td><td align="center" valign="middle" >ARRIVE</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >moderate</td></tr><tr><td align="center" valign="middle" >33</td><td align="center" valign="middle" >Autologous menstrual blood-derived stromal cells transplantation for severe Asherman’s syndrome</td><td align="center" valign="middle" >Jichun Tan</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >34</td><td align="center" valign="middle" >Autologous stem cell transplantation in refractory Asherman’s syndrome: A novel cell based therapy</td><td align="center" valign="middle" >Neeta Singh</td><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >35</td><td align="center" valign="middle" >Autologous cell therapy with CD1331 bone marrow-derived stem cells for refractory Asherman’s syndrome and endometrial atrophy: a pilot cohort study</td><td align="center" valign="middle" >Xavier Santamaria</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >36</td><td align="center" valign="middle" >Transplantation of collagen scaffold with autologous bone marrow mononuclear cells promotes functional endometrium reconstruction via down regulating ΔNp63 expressionin Asherman’s syndrome</td><td align="center" valign="middle" >Guangfeng Zhao</td><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr><tr><td align="center" valign="middle" >37</td><td align="center" valign="middle" >Allogeneic cell therapy using umbilical cord MSCs on collagen scaffolds for patients with recurrent uterine adhesion: a phase I clinical trial</td><td align="center" valign="middle" >Yun Cao</td><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >cohort</td><td align="center" valign="middle" >NOS</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >high</td></tr></tbody></table></table-wrap></table-wrap-group><p>NOS: Newcastle-Ottawa quality assessment scale, RCT: Random Clinical Trails, iCAHE: The International Center for Allied Health Evidence, ARRIVE: Animal Research: Reporting in Vivo Experiments</p><p>cell [<xref ref-type="bibr" rid="scirp.106827-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref23">23</xref>].</p></sec><sec id="s3_2"><title>3.2. Animal Experiments Results</title><p>There were more than ten researches illustrated that stem cells could repair uterine endometrium in animal models during the recent 10 years [<xref ref-type="bibr" rid="scirp.106827-ref24">24</xref>]. Here, we conclude four typical articles among them to illustrate the stem cells application for animal models.</p><p>According to Sevtap and Beril [<xref ref-type="bibr" rid="scirp.106827-ref25">25</xref>], they have designed the experiment to evaluate the effects of stem cells to induce endometrial proliferation and angiogenesis on Asherman’s Syndrome. This research resulted that the amount of fibrosis, vascularisation, inflammation and immune histochemical staining with vascular endothelial growth factor (VEGF), proliferating cell nuclear antigen (PCNA) and Ki-67 were evaluated in the uterine tissues. After mesenchymal stem cells (MSCs) therapy; fibrosis in mice uterine decreased but vascularisation and immune histochemical staining increased in the experimental side. This study also concluded that stem cells and estrogen were an extremely useful choose to induce regeneration of endometrium in Asherman Syndrome therapy. Similarly, Feryal Alawadhi et al. [<xref ref-type="bibr" rid="scirp.106827-ref26">26</xref>] Jianmei Wang et al. [<xref ref-type="bibr" rid="scirp.106827-ref27">27</xref>] and Yang et al. [<xref ref-type="bibr" rid="scirp.106827-ref28">28</xref>] conducted research that bone marrow-derived mesenchymal stem cells (BMSCs) were injected to adult female albino rats with uterine damage. They were observed that BMSCs transplantation was an original treatment for Asherman’s Syndrome and may also be helpful to prevent Asherman’s Syndrome after uterine injury.</p><p>The other researchers completed the animal experiments on rat model of IUAs and stem cell therapy for them, which reported that stem cells transplantation was a potential novel treatment for Asherman’s Syndrome and may also be useful to prevent Asherman’s Syndrome after uterine injury syndrome [<xref ref-type="bibr" rid="scirp.106827-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref31">31</xref>].</p></sec><sec id="s3_3"><title>3.3. Stem Cell Application in Human IUAs: Meta-Analysis</title><p>In recent ten years, there are several articles focusing on stem cells therapy in intrauterine adhesions and we have found five articles of human which are single arm studies focusing on this objection. Thus, we do the meta-analysis depending on them by software of meta-analyst [<xref ref-type="bibr" rid="scirp.106827-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref36">36</xref>].</p><p><xref ref-type="fig" rid="fig2">Figure 2</xref> shows the forest plots of age in the five studies which use random effect model because of P = 0.012. The figure results that the weight mean difference is 33.765% and 95% Confidence Interval (95% CI) is 33.330 to 34.201.</p><p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows that the endometrial thickness before stem cells treatment in these studies. And the weight mean difference (WMD) is 3.66 and 95% CI is 2.599 to 4.620, which results from random effect model by P &lt; 0.001. <xref ref-type="fig" rid="fig4">Figure 4</xref></p><p>shows that the endometrial thickness after stem cells treatment. In which, the WMD is 6.192 and 95% CI is 5.865 to 6.520, which also results from random effect model by P = 0.006. <xref ref-type="fig" rid="fig5">Figure 5</xref> illustrates that the improvement under hysteroscopy after stem cell therapy, but only three studies undergo it. And the forest plot shows that the estimated odd ratio is 0.892 (95% CI: 0.805, 0.907) resulting from fixed effect model by P = 0.3800.</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Along with development and progression of IUAs, fibrotic tissues gradually covered or replaced the normal endometrium and promoted the formation of IUAs. And inflammatory factor TGF-β has demonstrated to be a central mediator of the fibrotic response. Currently, Smad3 protein proves to an important signal transduction molecule that induces the activation of TGF-β and the binding of TGF with receptors to the signal transduce from the cytoplasm to the nucleus. Through the TGF/Smad3 pathway, collagen synthesis and extracellular matrix precipitates are increased, promoting the formation of tissue fiber scar [<xref ref-type="bibr" rid="scirp.106827-ref23">23</xref>]. Activation and abnormal expression of TGF-β1 can inhibit the expression of Matrix Metalloproteinase-9 (MMP-9), promote the expression of Tissue Inhibitor of Matrix Metalloproteinases-1 (TIMP-1), reduce the activity of proteolytic enzyme, then promote the formation of Extracellular Matrix (ECM) but not easy to be degraded, leading to the transformation of fibroblasts into myofibroblasts, and promote wound contraction [<xref ref-type="bibr" rid="scirp.106827-ref19">19</xref>]. The process of the pathogenesis of IUAs is complicated, other studies showed that the expression of MMP-9 and Nuclear Factor-κB (NF-κB) miRNA are also significantly higher in the endometrial sample from intrauterine adhesion compared to normal endometrial controls. Furthermore, the specific mechanism needs to be investigated [<xref ref-type="bibr" rid="scirp.106827-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.106827-ref38">38</xref>].</p><p>Although a couple of experiments have demonstrated the safety of stem cells transplantation as a therapeutic strategy for IUAs, the capability of self-renew of stem cell and the up-regulation of anti-inflammatory may induce uncontrolled cell growth and tumorigenesis.</p><p>As human clinical experiments result, we found that the age of IUAs under stem cells is about 33 years in four studies but one research which was written by Neeta Singh, included patients much younger than others (29.8). However, this study just integrated 6 cases that could not change the results significantly because of less weight. Thus, the bias of age is less. In addition, the endometrial thickness (3.61 mm) under ultrasound before treatment is rather thinner than normal ones (more than 5 mm), which may be the main reason for amenorrhea and infertility. Then, after stem cell therapy including intrauterine injection and vein injection, the thickness of endometrial (6.192 mm) is improved significantly. However, the ultrasound could not be the best standard for evaluating the effectiveness of therapy depending on the guideline. Three of them finish hysteroscopy after stem cell therapy and 40 amongst 46 patients in these studies get improved from severe IUAs to normal endometrial or moderate IUAs. Also, the improving symptoms could be the evaluation like normal menstruation, pregnancy and delivery. Depending on Xavier Santamaria study more than 50% patient pregnant and 16% patients got babies in full-term, as well as, 4 patients and 1 patient in study from Zhao et al. are reported to full-term and premature labor in 28 weeks(twins) respectively. Thus, in clinical trial reports, we conclude that stem cell could be a new therapeutic schedule for IUAs.</p><p>However, all these researches are single-arm studies without control groups for comparison because it may be difficult for clinic to finish comparing with other therapy. Furthermore, we can develop the stem cell therapy treating IUAs for more patients and implement multi-center clinical study and Random Clinical Tests (RCTs).</p></sec><sec id="s5"><title>Acknowledgements</title><p>We acknowledge the support of Beijing Hospital, National Center of Gerontology, National Cancer Center and Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, China. This work was supported by the Beijing Dongcheng Department of Science, Technology, and Information (BJ-2019-103 to Shaowei Wang). The authors in this work, including Sichen Zhang, Ying Mao, Shaowei Wang, Huiwen Zhang, Min Ma, Xingbo Long, declare no competing interests. There is not necessary of ethical approval.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Zhang, S.C., Mao, Y., Zhao, X.D., Zhang, H.W., Ma, M., Long, X.B. and Wang, S.W. (2021) Intrauterine Adhesions (IUAs) or Asherman’s Syndrome (AS) and the Stem Cells Treatment: A Systemic Review and Meta-Analysis. Journal of Biosciences and Medicines, 9, 105-118. https://doi.org/10.4236/jbm.2021.91009</p></sec><sec id="s8"><title>Abbreviation</title><p>IUAs = Intrauterine Adhesions.</p><p>AS = Asherman’s Syndrome.</p><p>MRI = Magnetic Resonance Imaging.</p><p>HSG = Hysterosalpingography.</p><p>ESGE = European Society of Gynecological Endoscopy.</p><p>ESH = European Society for Hysteroscopy.</p><p>AFS = American Fertility Society.</p><p>AAGL = American Association of Gynecologic Laparoscopists.</p><p>MenSCs = Menstrual blood derived Stromal Cells.</p><p>UC = Umbilical Cord.</p><p>MSCs = Mesenchymal Stromal Cells.</p><p>BMMNCs = Bone Marrow derived Mononuclear Cells.</p><p>NOS = Newcastle-Ottawa quality assessment scale.</p><p>WMD = Weight Mean Difference.</p><p>OR = Odds Ratio.</p><p>CI = Confidence Interval.</p><p>TGF-β= Transforming Growth Factors-β.</p><p>TNF-α = Tumor Necrosis Factor-α.</p><p>VEGF = Vascular Endothelial Growth Factor.</p><p>UCMSCs-EVs = Extracellular Vesicles derived from human Umbilical Cord Mesenchymal Stem Cells.</p><p>ERα = Estrogen Receptor α.</p><p>SDF-1/CXCR-4 = Stromal Derived Factor/Chemokine Receptor type 4.</p><p>bFGF = Fibroblast Growth Factor.</p><p>IL = Interleukin.</p><p>VEGF = Vascular Endothelial Growth Factor.</p><p>PCNA = Proliferating Cell Nuclear Antigen.</p><p>MMP-9 = Matrix Metalloproteinase-9.</p><p>TIMP-1 = Tissue Inhibitor of Matrix Metalloproteinases-1.</p><p>ECM = Extracellular Matrix.</p><p>NF-κB = Nuclear Factor-κB.</p><p>RCTs = Random Clinical Tests.</p></sec></body><back><ref-list><title>References</title><ref id="scirp.106827-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">(1988) The American Fertility Society Classifications of Adnexal Adhesions, Distal Tubal Occlusion, Tubal Occlusion Secondary to Tubal Ligation, Tubal Pregnancies, Mullerian Anomalies and Intrauterine Adhesions. 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