Loading…

Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy

Our primary objective was to evaluate the endometrial changes before and after the transfer of endometrial mesenchymal stem cells (enMSCs) in a population of thinned endometrium women, with absence or hypo-responsiveness to estrogen and repeated implantation failure (RIF). The secondary objective wa...

Full description

Saved in:
Bibliographic Details
Published in:JBRA assisted reproduction 2020, Vol.24 (2), p.118-127
Main Authors: Tersoglio, Alberto E, Tersoglio, Sebastian, Salatino, Dante R, Castro, Matías, Gonzalez, Adriana, Hinojosa, Mariana, Castellano, Onias
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c430t-98eacb6d09350396cb707b39445d680db65d5833ea89098f501afa47b1de27403
cites
container_end_page 127
container_issue 2
container_start_page 118
container_title JBRA assisted reproduction
container_volume 24
creator Tersoglio, Alberto E
Tersoglio, Sebastian
Salatino, Dante R
Castro, Matías
Gonzalez, Adriana
Hinojosa, Mariana
Castellano, Onias
description Our primary objective was to evaluate the endometrial changes before and after the transfer of endometrial mesenchymal stem cells (enMSCs) in a population of thinned endometrium women, with absence or hypo-responsiveness to estrogen and repeated implantation failure (RIF). The secondary objective was to evaluate the clinical outcomes of the intervention in terms of clinical pregnancy (CP), early abortions, ongoing pregnancy and live birth delivery rate (LBDR) per in vitro fertilization (IVF) cycle. A longitudinal and experimental study. The intervention was defined as "subendometrial inoculation of enMSCs," and the post-intervention changes were evaluated by the following variables: endometrial thickness (Eth), endometrial flow cytometry (enFC), endometrial histopathology (enHP) and endometrial immunohistochemistry (enIHQ). The variables were analyzed after the intervention (Post-treatment) regarding previous values (Pretreatment). Eth values before and after treatment with enMSCs were 5.24±1.24 mm vs. 9.93±0.77 (p=0.000), respectively. Endometrial Flow Cytometry showed significant differences in favor of Normalized variables in the post-treatment assessment, associated with the pretreatment, LT/Li, LB/Li, NK/Li, CD8/CD3+ and CD4/CD8 (p≤0.015), respectively. Only two variables Li/PC and CD4/CD3 had NS (p=0.167 and 0.118). A similar analysis was performed on enHP with an HP increase post-treatment (p=0.007). The CP rate was 79.31% (23/29), a live birth delivery rate per embryo transfer was 45.45% (10/22) and ongoing pregnancy 7/29 (24.14%). Subendometrial enMSCs inoculation produces a significant increase in endometrial thickness; normalize the enHP, enIHQ and enFC. As a result, IVF after treatment with enMSCs yields a higher rate of CP and LBDR.
doi_str_mv 10.5935/1518-0557.20190061
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7169908</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2302471186</sourcerecordid><originalsourceid>FETCH-LOGICAL-c430t-98eacb6d09350396cb707b39445d680db65d5833ea89098f501afa47b1de27403</originalsourceid><addsrcrecordid>eNpdkUFr3DAQhUVpaUKaP9BDEfTSy25HliVLl0IIbRMIFEpyFrI93lWwZVeSt_icPx6ZJEvaizRI3zzN0yPkI4Ot0Fx8ZYKpDQhRbQtgGkCyN-T0ePj2VX1CzmO8B8gYK3gJ78kJZ0JprtkpefiNO_QYbHIHpGmfq2mh9ULRt-OAKTjb0wEj-ma_DLmOCQfaYN9H6nxuyMsRnQf616U9DTihTdhSN0y99SmLj5521vVzwC29oH484CqVn8Xd8oG862wf8fx5PyN3P77fXl5tbn79vL68uNk0JYe00QptU8sWsn3gWjZ1BVXNdVmKVipoaylaoThHqzRo1QlgtrNlVbMWi6oEfka-PelOcz1g26DPA_RmCm6wYTGjdebfG-_2ZjceTMWk1qCywJdngTD-mTEmM7i4_oX1OM7RFByKsmJMyYx-_g-9H-fgs71MaalKLYsiU8UT1YQxxoDdcRgGZo3ZrCmaNUXzEnNu-vTaxrHlJVT-CJnupU0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2396849622</pqid></control><display><type>article</type><title>Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Tersoglio, Alberto E ; Tersoglio, Sebastian ; Salatino, Dante R ; Castro, Matías ; Gonzalez, Adriana ; Hinojosa, Mariana ; Castellano, Onias</creator><creatorcontrib>Tersoglio, Alberto E ; Tersoglio, Sebastian ; Salatino, Dante R ; Castro, Matías ; Gonzalez, Adriana ; Hinojosa, Mariana ; Castellano, Onias</creatorcontrib><description>Our primary objective was to evaluate the endometrial changes before and after the transfer of endometrial mesenchymal stem cells (enMSCs) in a population of thinned endometrium women, with absence or hypo-responsiveness to estrogen and repeated implantation failure (RIF). The secondary objective was to evaluate the clinical outcomes of the intervention in terms of clinical pregnancy (CP), early abortions, ongoing pregnancy and live birth delivery rate (LBDR) per in vitro fertilization (IVF) cycle. A longitudinal and experimental study. The intervention was defined as "subendometrial inoculation of enMSCs," and the post-intervention changes were evaluated by the following variables: endometrial thickness (Eth), endometrial flow cytometry (enFC), endometrial histopathology (enHP) and endometrial immunohistochemistry (enIHQ). The variables were analyzed after the intervention (Post-treatment) regarding previous values (Pretreatment). Eth values before and after treatment with enMSCs were 5.24±1.24 mm vs. 9.93±0.77 (p=0.000), respectively. Endometrial Flow Cytometry showed significant differences in favor of Normalized variables in the post-treatment assessment, associated with the pretreatment, LT/Li, LB/Li, NK/Li, CD8/CD3+ and CD4/CD8 (p≤0.015), respectively. Only two variables Li/PC and CD4/CD3 had NS (p=0.167 and 0.118). A similar analysis was performed on enHP with an HP increase post-treatment (p=0.007). The CP rate was 79.31% (23/29), a live birth delivery rate per embryo transfer was 45.45% (10/22) and ongoing pregnancy 7/29 (24.14%). Subendometrial enMSCs inoculation produces a significant increase in endometrial thickness; normalize the enHP, enIHQ and enFC. As a result, IVF after treatment with enMSCs yields a higher rate of CP and LBDR.</description><identifier>ISSN: 1518-0557</identifier><identifier>ISSN: 1517-5693</identifier><identifier>EISSN: 1518-0557</identifier><identifier>DOI: 10.5935/1518-0557.20190061</identifier><identifier>PMID: 31589391</identifier><language>eng</language><publisher>Brazil: Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</publisher><subject>Angiogenesis ; Cytokines ; Embryos ; Endometrium ; Original ; Patients ; Pregnancy ; Quality ; Ultrasonic imaging ; Vascular endothelial growth factor</subject><ispartof>JBRA assisted reproduction, 2020, Vol.24 (2), p.118-127</ispartof><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-98eacb6d09350396cb707b39445d680db65d5833ea89098f501afa47b1de27403</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2396849622/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2396849622?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,25753,27923,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31589391$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tersoglio, Alberto E</creatorcontrib><creatorcontrib>Tersoglio, Sebastian</creatorcontrib><creatorcontrib>Salatino, Dante R</creatorcontrib><creatorcontrib>Castro, Matías</creatorcontrib><creatorcontrib>Gonzalez, Adriana</creatorcontrib><creatorcontrib>Hinojosa, Mariana</creatorcontrib><creatorcontrib>Castellano, Onias</creatorcontrib><title>Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy</title><title>JBRA assisted reproduction</title><addtitle>JBRA Assist Reprod</addtitle><description>Our primary objective was to evaluate the endometrial changes before and after the transfer of endometrial mesenchymal stem cells (enMSCs) in a population of thinned endometrium women, with absence or hypo-responsiveness to estrogen and repeated implantation failure (RIF). The secondary objective was to evaluate the clinical outcomes of the intervention in terms of clinical pregnancy (CP), early abortions, ongoing pregnancy and live birth delivery rate (LBDR) per in vitro fertilization (IVF) cycle. A longitudinal and experimental study. The intervention was defined as "subendometrial inoculation of enMSCs," and the post-intervention changes were evaluated by the following variables: endometrial thickness (Eth), endometrial flow cytometry (enFC), endometrial histopathology (enHP) and endometrial immunohistochemistry (enIHQ). The variables were analyzed after the intervention (Post-treatment) regarding previous values (Pretreatment). Eth values before and after treatment with enMSCs were 5.24±1.24 mm vs. 9.93±0.77 (p=0.000), respectively. Endometrial Flow Cytometry showed significant differences in favor of Normalized variables in the post-treatment assessment, associated with the pretreatment, LT/Li, LB/Li, NK/Li, CD8/CD3+ and CD4/CD8 (p≤0.015), respectively. Only two variables Li/PC and CD4/CD3 had NS (p=0.167 and 0.118). A similar analysis was performed on enHP with an HP increase post-treatment (p=0.007). The CP rate was 79.31% (23/29), a live birth delivery rate per embryo transfer was 45.45% (10/22) and ongoing pregnancy 7/29 (24.14%). Subendometrial enMSCs inoculation produces a significant increase in endometrial thickness; normalize the enHP, enIHQ and enFC. As a result, IVF after treatment with enMSCs yields a higher rate of CP and LBDR.</description><subject>Angiogenesis</subject><subject>Cytokines</subject><subject>Embryos</subject><subject>Endometrium</subject><subject>Original</subject><subject>Patients</subject><subject>Pregnancy</subject><subject>Quality</subject><subject>Ultrasonic imaging</subject><subject>Vascular endothelial growth factor</subject><issn>1518-0557</issn><issn>1517-5693</issn><issn>1518-0557</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkUFr3DAQhUVpaUKaP9BDEfTSy25HliVLl0IIbRMIFEpyFrI93lWwZVeSt_icPx6ZJEvaizRI3zzN0yPkI4Ot0Fx8ZYKpDQhRbQtgGkCyN-T0ePj2VX1CzmO8B8gYK3gJ78kJZ0JprtkpefiNO_QYbHIHpGmfq2mh9ULRt-OAKTjb0wEj-ma_DLmOCQfaYN9H6nxuyMsRnQf616U9DTihTdhSN0y99SmLj5521vVzwC29oH484CqVn8Xd8oG862wf8fx5PyN3P77fXl5tbn79vL68uNk0JYe00QptU8sWsn3gWjZ1BVXNdVmKVipoaylaoThHqzRo1QlgtrNlVbMWi6oEfka-PelOcz1g26DPA_RmCm6wYTGjdebfG-_2ZjceTMWk1qCywJdngTD-mTEmM7i4_oX1OM7RFByKsmJMyYx-_g-9H-fgs71MaalKLYsiU8UT1YQxxoDdcRgGZo3ZrCmaNUXzEnNu-vTaxrHlJVT-CJnupU0</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Tersoglio, Alberto E</creator><creator>Tersoglio, Sebastian</creator><creator>Salatino, Dante R</creator><creator>Castro, Matías</creator><creator>Gonzalez, Adriana</creator><creator>Hinojosa, Mariana</creator><creator>Castellano, Onias</creator><general>Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</general><general>Brazilian Society of Assisted Reproduction</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2020</creationdate><title>Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy</title><author>Tersoglio, Alberto E ; Tersoglio, Sebastian ; Salatino, Dante R ; Castro, Matías ; Gonzalez, Adriana ; Hinojosa, Mariana ; Castellano, Onias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-98eacb6d09350396cb707b39445d680db65d5833ea89098f501afa47b1de27403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Angiogenesis</topic><topic>Cytokines</topic><topic>Embryos</topic><topic>Endometrium</topic><topic>Original</topic><topic>Patients</topic><topic>Pregnancy</topic><topic>Quality</topic><topic>Ultrasonic imaging</topic><topic>Vascular endothelial growth factor</topic><toplevel>online_resources</toplevel><creatorcontrib>Tersoglio, Alberto E</creatorcontrib><creatorcontrib>Tersoglio, Sebastian</creatorcontrib><creatorcontrib>Salatino, Dante R</creatorcontrib><creatorcontrib>Castro, Matías</creatorcontrib><creatorcontrib>Gonzalez, Adriana</creatorcontrib><creatorcontrib>Hinojosa, Mariana</creatorcontrib><creatorcontrib>Castellano, Onias</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JBRA assisted reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tersoglio, Alberto E</au><au>Tersoglio, Sebastian</au><au>Salatino, Dante R</au><au>Castro, Matías</au><au>Gonzalez, Adriana</au><au>Hinojosa, Mariana</au><au>Castellano, Onias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy</atitle><jtitle>JBRA assisted reproduction</jtitle><addtitle>JBRA Assist Reprod</addtitle><date>2020</date><risdate>2020</risdate><volume>24</volume><issue>2</issue><spage>118</spage><epage>127</epage><pages>118-127</pages><issn>1518-0557</issn><issn>1517-5693</issn><eissn>1518-0557</eissn><abstract>Our primary objective was to evaluate the endometrial changes before and after the transfer of endometrial mesenchymal stem cells (enMSCs) in a population of thinned endometrium women, with absence or hypo-responsiveness to estrogen and repeated implantation failure (RIF). The secondary objective was to evaluate the clinical outcomes of the intervention in terms of clinical pregnancy (CP), early abortions, ongoing pregnancy and live birth delivery rate (LBDR) per in vitro fertilization (IVF) cycle. A longitudinal and experimental study. The intervention was defined as "subendometrial inoculation of enMSCs," and the post-intervention changes were evaluated by the following variables: endometrial thickness (Eth), endometrial flow cytometry (enFC), endometrial histopathology (enHP) and endometrial immunohistochemistry (enIHQ). The variables were analyzed after the intervention (Post-treatment) regarding previous values (Pretreatment). Eth values before and after treatment with enMSCs were 5.24±1.24 mm vs. 9.93±0.77 (p=0.000), respectively. Endometrial Flow Cytometry showed significant differences in favor of Normalized variables in the post-treatment assessment, associated with the pretreatment, LT/Li, LB/Li, NK/Li, CD8/CD3+ and CD4/CD8 (p≤0.015), respectively. Only two variables Li/PC and CD4/CD3 had NS (p=0.167 and 0.118). A similar analysis was performed on enHP with an HP increase post-treatment (p=0.007). The CP rate was 79.31% (23/29), a live birth delivery rate per embryo transfer was 45.45% (10/22) and ongoing pregnancy 7/29 (24.14%). Subendometrial enMSCs inoculation produces a significant increase in endometrial thickness; normalize the enHP, enIHQ and enFC. As a result, IVF after treatment with enMSCs yields a higher rate of CP and LBDR.</abstract><cop>Brazil</cop><pub>Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</pub><pmid>31589391</pmid><doi>10.5935/1518-0557.20190061</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1518-0557
ispartof JBRA assisted reproduction, 2020, Vol.24 (2), p.118-127
issn 1518-0557
1517-5693
1518-0557
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7169908
source Publicly Available Content Database; PubMed Central
subjects Angiogenesis
Cytokines
Embryos
Endometrium
Original
Patients
Pregnancy
Quality
Ultrasonic imaging
Vascular endothelial growth factor
title Regenerative therapy by endometrial mesenchymal stem cells in thin endometrium with repeated implantation failure. A novel strategy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T10%3A32%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regenerative%20therapy%20by%20endometrial%20mesenchymal%20stem%20cells%20in%20thin%20endometrium%20with%20repeated%20implantation%20failure.%20A%20novel%20strategy&rft.jtitle=JBRA%20assisted%20reproduction&rft.au=Tersoglio,%20Alberto%20E&rft.date=2020&rft.volume=24&rft.issue=2&rft.spage=118&rft.epage=127&rft.pages=118-127&rft.issn=1518-0557&rft.eissn=1518-0557&rft_id=info:doi/10.5935/1518-0557.20190061&rft_dat=%3Cproquest_pubme%3E2302471186%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c430t-98eacb6d09350396cb707b39445d680db65d5833ea89098f501afa47b1de27403%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2396849622&rft_id=info:pmid/31589391&rfr_iscdi=true