Mesenchymal stem cell therapy in hypertrophic and keloid scars
Scars are the normal outcome of wound repair and involve a co-ordinated inflammatory and fibrotic process. When a scar does not resolve, uncontrolled chronic inflammation can persist and elicits excessive scarring that leads to a range of abnormal phenotypes such as hypertrophic and keloid scars. Th...
Gespeichert in:
Veröffentlicht in: | Cell and tissue research 2021-03, Vol.383 (3), p.915-930 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 930 |
---|---|
container_issue | 3 |
container_start_page | 915 |
container_title | Cell and tissue research |
container_volume | 383 |
creator | Bojanic, Christine To, Kendrick Hatoum, Adam Shea, Jessie Seah, K. T. Matthew Khan, Wasim Malata, Charles M. |
description | Scars are the normal outcome of wound repair and involve a co-ordinated inflammatory and fibrotic process. When a scar does not resolve, uncontrolled chronic inflammation can persist and elicits excessive scarring that leads to a range of abnormal phenotypes such as hypertrophic and keloid scars. These pathologies result in significant impairment of quality of life over a long period of time. Existing treatment options are generally unsatisfactory, and there is mounting interest in innovative cell-based therapies. Despite the interest in mesenchymal stem cells (MSCs), there is yet to be a human clinical trial that investigates the potential of MSCs in treating abnormal scarring. A synthesis of existing evidence of animal studies may therefore provide insight into the barriers to human application. The aim of this PRISMA systematic review was to evaluate the effectiveness of MSC transplantation in the treatment of hypertrophic and keloid scars in in vivo models. A total of 11 case-control studies were identified that treated a total of 156 subjects with MSCs or MSC-conditioned media. Ten studies assessed hypertrophic scars, and one looked at keloid scars. All studies evaluated scars in terms of macroscopic and histological appearances and most incorporated immunohistochemistry. The included studies all found improvements in the above outcomes with MSC or MSC-conditioned media without complications. The studies reviewed support a role for MSC therapy in treating scars that needs further exploration. The transferability of these findings to humans is limited by factors such as the reliability and validity of the disease model, the need to identify the optimal MSC cell source, and the outcome measures employed. |
doi_str_mv | 10.1007/s00441-020-03361-z |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7960584</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A656117272</galeid><sourcerecordid>A656117272</sourcerecordid><originalsourceid>FETCH-LOGICAL-c638t-a84023ce80b8ca4c90c9a7533375c6df63e3e6e97af30c15123c76c761893c2c3</originalsourceid><addsrcrecordid>eNp9kl1rFDEUhoModq3-AS9kQBBvpp58TJK5KZTiF1S8UfAupJkzO6kzyZrMCNtfb9atbVdEEgjkPO-bnMNLyHMKJxRAvckAQtAaGNTAuaT19QOyooKzGrTSD8kKOLBaSfntiDzJ-QqACinbx-SIc65l2zYrcvoJMwY3bCc7VnnGqXI4jtU8YLKbbeVDNWw3mOYUN4N3lQ1d9R3H6LsqO5vyU_Kot2PGZzfnMfn67u2X8w_1xef3H8_PLmonuZ5rqwUw7lDDpXZWuBZca1VTvqEaJ7tecuQosVW25-BoQwusZNlUt9wxx4_J6d53s1xO2DkMc7Kj2SQ_2bQ10XpzWAl-MOv406hWQqNFMXh9Y5DijwXzbCafd63agHHJhgkltGiA64K-_Au9iksKpT3DGqC8UYyzO2ptRzQ-9LG863am5kw2klLF1I46-QdVVoeTdzFg78v9geDVPcGAdpyHHMdl9jHkQ5DtQZdizgn722FQMLt4mH08TImH-R0Pc11EL-6P8VbyJw8F4Hsgl1JYY7rr_T-2vwDjo8OD</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2501357232</pqid></control><display><type>article</type><title>Mesenchymal stem cell therapy in hypertrophic and keloid scars</title><source>SpringerLink Journals</source><creator>Bojanic, Christine ; To, Kendrick ; Hatoum, Adam ; Shea, Jessie ; Seah, K. T. Matthew ; Khan, Wasim ; Malata, Charles M.</creator><creatorcontrib>Bojanic, Christine ; To, Kendrick ; Hatoum, Adam ; Shea, Jessie ; Seah, K. T. Matthew ; Khan, Wasim ; Malata, Charles M.</creatorcontrib><description>Scars are the normal outcome of wound repair and involve a co-ordinated inflammatory and fibrotic process. When a scar does not resolve, uncontrolled chronic inflammation can persist and elicits excessive scarring that leads to a range of abnormal phenotypes such as hypertrophic and keloid scars. These pathologies result in significant impairment of quality of life over a long period of time. Existing treatment options are generally unsatisfactory, and there is mounting interest in innovative cell-based therapies. Despite the interest in mesenchymal stem cells (MSCs), there is yet to be a human clinical trial that investigates the potential of MSCs in treating abnormal scarring. A synthesis of existing evidence of animal studies may therefore provide insight into the barriers to human application. The aim of this PRISMA systematic review was to evaluate the effectiveness of MSC transplantation in the treatment of hypertrophic and keloid scars in in vivo models. A total of 11 case-control studies were identified that treated a total of 156 subjects with MSCs or MSC-conditioned media. Ten studies assessed hypertrophic scars, and one looked at keloid scars. All studies evaluated scars in terms of macroscopic and histological appearances and most incorporated immunohistochemistry. The included studies all found improvements in the above outcomes with MSC or MSC-conditioned media without complications. The studies reviewed support a role for MSC therapy in treating scars that needs further exploration. The transferability of these findings to humans is limited by factors such as the reliability and validity of the disease model, the need to identify the optimal MSC cell source, and the outcome measures employed.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-020-03361-z</identifier><identifier>PMID: 33386995</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analysis ; Biomedical and Life Sciences ; Biomedicine ; Care and treatment ; Cell therapy ; Human Genetics ; Immunohistochemistry ; Inflammation ; Medical colleges ; Medical research ; Medicine, Experimental ; Mesenchymal stem cells ; Molecular Medicine ; Phenotypes ; Proteomics ; Quality of life ; Review ; Scars ; Stem cell transplantation ; Stem cells ; Transplantation ; Wound healing</subject><ispartof>Cell and tissue research, 2021-03, Vol.383 (3), p.915-930</ispartof><rights>The Author(s) 2020</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s) 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c638t-a84023ce80b8ca4c90c9a7533375c6df63e3e6e97af30c15123c76c761893c2c3</citedby><cites>FETCH-LOGICAL-c638t-a84023ce80b8ca4c90c9a7533375c6df63e3e6e97af30c15123c76c761893c2c3</cites><orcidid>0000-0001-9262-7190</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-020-03361-z$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-020-03361-z$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33386995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bojanic, Christine</creatorcontrib><creatorcontrib>To, Kendrick</creatorcontrib><creatorcontrib>Hatoum, Adam</creatorcontrib><creatorcontrib>Shea, Jessie</creatorcontrib><creatorcontrib>Seah, K. T. Matthew</creatorcontrib><creatorcontrib>Khan, Wasim</creatorcontrib><creatorcontrib>Malata, Charles M.</creatorcontrib><title>Mesenchymal stem cell therapy in hypertrophic and keloid scars</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>Scars are the normal outcome of wound repair and involve a co-ordinated inflammatory and fibrotic process. When a scar does not resolve, uncontrolled chronic inflammation can persist and elicits excessive scarring that leads to a range of abnormal phenotypes such as hypertrophic and keloid scars. These pathologies result in significant impairment of quality of life over a long period of time. Existing treatment options are generally unsatisfactory, and there is mounting interest in innovative cell-based therapies. Despite the interest in mesenchymal stem cells (MSCs), there is yet to be a human clinical trial that investigates the potential of MSCs in treating abnormal scarring. A synthesis of existing evidence of animal studies may therefore provide insight into the barriers to human application. The aim of this PRISMA systematic review was to evaluate the effectiveness of MSC transplantation in the treatment of hypertrophic and keloid scars in in vivo models. A total of 11 case-control studies were identified that treated a total of 156 subjects with MSCs or MSC-conditioned media. Ten studies assessed hypertrophic scars, and one looked at keloid scars. All studies evaluated scars in terms of macroscopic and histological appearances and most incorporated immunohistochemistry. The included studies all found improvements in the above outcomes with MSC or MSC-conditioned media without complications. The studies reviewed support a role for MSC therapy in treating scars that needs further exploration. The transferability of these findings to humans is limited by factors such as the reliability and validity of the disease model, the need to identify the optimal MSC cell source, and the outcome measures employed.</description><subject>Analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Care and treatment</subject><subject>Cell therapy</subject><subject>Human Genetics</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Medical colleges</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Mesenchymal stem cells</subject><subject>Molecular Medicine</subject><subject>Phenotypes</subject><subject>Proteomics</subject><subject>Quality of life</subject><subject>Review</subject><subject>Scars</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Transplantation</subject><subject>Wound healing</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kl1rFDEUhoModq3-AS9kQBBvpp58TJK5KZTiF1S8UfAupJkzO6kzyZrMCNtfb9atbVdEEgjkPO-bnMNLyHMKJxRAvckAQtAaGNTAuaT19QOyooKzGrTSD8kKOLBaSfntiDzJ-QqACinbx-SIc65l2zYrcvoJMwY3bCc7VnnGqXI4jtU8YLKbbeVDNWw3mOYUN4N3lQ1d9R3H6LsqO5vyU_Kot2PGZzfnMfn67u2X8w_1xef3H8_PLmonuZ5rqwUw7lDDpXZWuBZca1VTvqEaJ7tecuQosVW25-BoQwusZNlUt9wxx4_J6d53s1xO2DkMc7Kj2SQ_2bQ10XpzWAl-MOv406hWQqNFMXh9Y5DijwXzbCafd63agHHJhgkltGiA64K-_Au9iksKpT3DGqC8UYyzO2ptRzQ-9LG863am5kw2klLF1I46-QdVVoeTdzFg78v9geDVPcGAdpyHHMdl9jHkQ5DtQZdizgn722FQMLt4mH08TImH-R0Pc11EL-6P8VbyJw8F4Hsgl1JYY7rr_T-2vwDjo8OD</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Bojanic, Christine</creator><creator>To, Kendrick</creator><creator>Hatoum, Adam</creator><creator>Shea, Jessie</creator><creator>Seah, K. T. Matthew</creator><creator>Khan, Wasim</creator><creator>Malata, Charles M.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9262-7190</orcidid></search><sort><creationdate>20210301</creationdate><title>Mesenchymal stem cell therapy in hypertrophic and keloid scars</title><author>Bojanic, Christine ; To, Kendrick ; Hatoum, Adam ; Shea, Jessie ; Seah, K. T. Matthew ; Khan, Wasim ; Malata, Charles M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c638t-a84023ce80b8ca4c90c9a7533375c6df63e3e6e97af30c15123c76c761893c2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Care and treatment</topic><topic>Cell therapy</topic><topic>Human Genetics</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Medical colleges</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Mesenchymal stem cells</topic><topic>Molecular Medicine</topic><topic>Phenotypes</topic><topic>Proteomics</topic><topic>Quality of life</topic><topic>Review</topic><topic>Scars</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Transplantation</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bojanic, Christine</creatorcontrib><creatorcontrib>To, Kendrick</creatorcontrib><creatorcontrib>Hatoum, Adam</creatorcontrib><creatorcontrib>Shea, Jessie</creatorcontrib><creatorcontrib>Seah, K. T. Matthew</creatorcontrib><creatorcontrib>Khan, Wasim</creatorcontrib><creatorcontrib>Malata, Charles M.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bojanic, Christine</au><au>To, Kendrick</au><au>Hatoum, Adam</au><au>Shea, Jessie</au><au>Seah, K. T. Matthew</au><au>Khan, Wasim</au><au>Malata, Charles M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stem cell therapy in hypertrophic and keloid scars</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>383</volume><issue>3</issue><spage>915</spage><epage>930</epage><pages>915-930</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>Scars are the normal outcome of wound repair and involve a co-ordinated inflammatory and fibrotic process. When a scar does not resolve, uncontrolled chronic inflammation can persist and elicits excessive scarring that leads to a range of abnormal phenotypes such as hypertrophic and keloid scars. These pathologies result in significant impairment of quality of life over a long period of time. Existing treatment options are generally unsatisfactory, and there is mounting interest in innovative cell-based therapies. Despite the interest in mesenchymal stem cells (MSCs), there is yet to be a human clinical trial that investigates the potential of MSCs in treating abnormal scarring. A synthesis of existing evidence of animal studies may therefore provide insight into the barriers to human application. The aim of this PRISMA systematic review was to evaluate the effectiveness of MSC transplantation in the treatment of hypertrophic and keloid scars in in vivo models. A total of 11 case-control studies were identified that treated a total of 156 subjects with MSCs or MSC-conditioned media. Ten studies assessed hypertrophic scars, and one looked at keloid scars. All studies evaluated scars in terms of macroscopic and histological appearances and most incorporated immunohistochemistry. The included studies all found improvements in the above outcomes with MSC or MSC-conditioned media without complications. The studies reviewed support a role for MSC therapy in treating scars that needs further exploration. The transferability of these findings to humans is limited by factors such as the reliability and validity of the disease model, the need to identify the optimal MSC cell source, and the outcome measures employed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33386995</pmid><doi>10.1007/s00441-020-03361-z</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-9262-7190</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0302-766X |
ispartof | Cell and tissue research, 2021-03, Vol.383 (3), p.915-930 |
issn | 0302-766X 1432-0878 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7960584 |
source | SpringerLink Journals |
subjects | Analysis Biomedical and Life Sciences Biomedicine Care and treatment Cell therapy Human Genetics Immunohistochemistry Inflammation Medical colleges Medical research Medicine, Experimental Mesenchymal stem cells Molecular Medicine Phenotypes Proteomics Quality of life Review Scars Stem cell transplantation Stem cells Transplantation Wound healing |
title | Mesenchymal stem cell therapy in hypertrophic and keloid scars |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A11%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mesenchymal%20stem%20cell%20therapy%20in%20hypertrophic%20and%20keloid%20scars&rft.jtitle=Cell%20and%20tissue%20research&rft.au=Bojanic,%20Christine&rft.date=2021-03-01&rft.volume=383&rft.issue=3&rft.spage=915&rft.epage=930&rft.pages=915-930&rft.issn=0302-766X&rft.eissn=1432-0878&rft_id=info:doi/10.1007/s00441-020-03361-z&rft_dat=%3Cgale_pubme%3EA656117272%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2501357232&rft_id=info:pmid/33386995&rft_galeid=A656117272&rfr_iscdi=true |