Prevention of post‐operative adhesions: Model development and pilot outcomes of human placental stem cell‐based interventions
Background Abdominal adhesions are the most common surgical complication and without reliable prophylactics. This study presents a novel rat model for abdominal adhesions and reports pilot results of human placental stem cell (hPSC)‐based therapies. Methods Forty‐four (n = 44) male Sprague–Dawley ra...
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Veröffentlicht in: | Transfusion (Philadelphia, Pa.) Pa.), 2024-06, Vol.64 (6), p.1059-1067 |
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creator | Carmichael, Samuel P. Chandra, Prafulla K. Vaughan, John W. Kline, David M. Ip, Edward H. Holcomb, John B. Atala, Anthony |
description | Background
Abdominal adhesions are the most common surgical complication and without reliable prophylactics. This study presents a novel rat model for abdominal adhesions and reports pilot results of human placental stem cell (hPSC)‐based therapies.
Methods
Forty‐four (n = 44) male Sprague–Dawley rats (250‐350 g) were used in the experiment. Of these, thirty‐eight (n = 38) were included in a preliminary data set to determine a minimum treatment effect. Adhesions were created in a reproducible model to the abdominal wall and between organs. Experimental groups included the control group (Model No Treatment, MNT), Plasmalyte A (Media Alone, MA, 10 mL), hPSC (5 × 106 cells/10 mL Plasmalyte A), hPSC‐CM (hPSC secretome, conditioned media) in 10 mL Plasmalyte A, Seprafilm™ (Baxter, Deerfield, IL), and sham animals (laparotomy only). Treatments were inserted intraperitoneally (IP) and the study period was 14 days post‐operation. Results are reported as the difference between means of an index statistic (AIS, Animal Index Score) and compared by ANOVA with pairwise comparison.
Results
The overall mean AIS was 23 (SD 6.16) for the MNT group with an average of 75% of ischemic buttons involved in abdominal adhesions. Treatment groups MA (mean overall AIS 17.33 SD 6.4), hPSC (mean overall AIS 13.86 SD 5.01), hPSC‐CM (mean overall AIS 13.13 SD 6.15), and Seprafilm (mean overall AIS 13.43 SD 9.11) generated effect sizes of 5.67, 9.14, 9.87, and 9.57 decrease in mean overall AIS, respectively, versus the MNT.
Discussion
The presented rat model and scoring system represent the clinical adhesion disease process. hPSC‐based interventions significantly reduce abdominal adhesions in this pilot dataset. |
doi_str_mv | 10.1111/trf.17859 |
format | Article |
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Abdominal adhesions are the most common surgical complication and without reliable prophylactics. This study presents a novel rat model for abdominal adhesions and reports pilot results of human placental stem cell (hPSC)‐based therapies.
Methods
Forty‐four (n = 44) male Sprague–Dawley rats (250‐350 g) were used in the experiment. Of these, thirty‐eight (n = 38) were included in a preliminary data set to determine a minimum treatment effect. Adhesions were created in a reproducible model to the abdominal wall and between organs. Experimental groups included the control group (Model No Treatment, MNT), Plasmalyte A (Media Alone, MA, 10 mL), hPSC (5 × 106 cells/10 mL Plasmalyte A), hPSC‐CM (hPSC secretome, conditioned media) in 10 mL Plasmalyte A, Seprafilm™ (Baxter, Deerfield, IL), and sham animals (laparotomy only). Treatments were inserted intraperitoneally (IP) and the study period was 14 days post‐operation. Results are reported as the difference between means of an index statistic (AIS, Animal Index Score) and compared by ANOVA with pairwise comparison.
Results
The overall mean AIS was 23 (SD 6.16) for the MNT group with an average of 75% of ischemic buttons involved in abdominal adhesions. Treatment groups MA (mean overall AIS 17.33 SD 6.4), hPSC (mean overall AIS 13.86 SD 5.01), hPSC‐CM (mean overall AIS 13.13 SD 6.15), and Seprafilm (mean overall AIS 13.43 SD 9.11) generated effect sizes of 5.67, 9.14, 9.87, and 9.57 decrease in mean overall AIS, respectively, versus the MNT.
Discussion
The presented rat model and scoring system represent the clinical adhesion disease process. hPSC‐based interventions significantly reduce abdominal adhesions in this pilot dataset.</description><identifier>ISSN: 0041-1132</identifier><identifier>ISSN: 1537-2995</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.17859</identifier><identifier>PMID: 38693056</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Abdomen ; Abdominal wall ; adhesions ; animal model ; bowel obstruction ; Health services ; Ischemia ; Mean ; Placenta ; regenerative medicine ; Secretome ; Stem cells ; Variance analysis</subject><ispartof>Transfusion (Philadelphia, Pa.), 2024-06, Vol.64 (6), p.1059-1067</ispartof><rights>2024 AABB.</rights><rights>2024 AABB</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3139-84f8f2613d0001a08488898d1cf399e08109e93cae5fffd94f6df60d754a2eb63</cites><orcidid>0000-0003-0237-4244 ; 0000-0001-8312-9157</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftrf.17859$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.17859$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38693056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carmichael, Samuel P.</creatorcontrib><creatorcontrib>Chandra, Prafulla K.</creatorcontrib><creatorcontrib>Vaughan, John W.</creatorcontrib><creatorcontrib>Kline, David M.</creatorcontrib><creatorcontrib>Ip, Edward H.</creatorcontrib><creatorcontrib>Holcomb, John B.</creatorcontrib><creatorcontrib>Atala, Anthony</creatorcontrib><title>Prevention of post‐operative adhesions: Model development and pilot outcomes of human placental stem cell‐based interventions</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>Background
Abdominal adhesions are the most common surgical complication and without reliable prophylactics. This study presents a novel rat model for abdominal adhesions and reports pilot results of human placental stem cell (hPSC)‐based therapies.
Methods
Forty‐four (n = 44) male Sprague–Dawley rats (250‐350 g) were used in the experiment. Of these, thirty‐eight (n = 38) were included in a preliminary data set to determine a minimum treatment effect. Adhesions were created in a reproducible model to the abdominal wall and between organs. Experimental groups included the control group (Model No Treatment, MNT), Plasmalyte A (Media Alone, MA, 10 mL), hPSC (5 × 106 cells/10 mL Plasmalyte A), hPSC‐CM (hPSC secretome, conditioned media) in 10 mL Plasmalyte A, Seprafilm™ (Baxter, Deerfield, IL), and sham animals (laparotomy only). Treatments were inserted intraperitoneally (IP) and the study period was 14 days post‐operation. Results are reported as the difference between means of an index statistic (AIS, Animal Index Score) and compared by ANOVA with pairwise comparison.
Results
The overall mean AIS was 23 (SD 6.16) for the MNT group with an average of 75% of ischemic buttons involved in abdominal adhesions. Treatment groups MA (mean overall AIS 17.33 SD 6.4), hPSC (mean overall AIS 13.86 SD 5.01), hPSC‐CM (mean overall AIS 13.13 SD 6.15), and Seprafilm (mean overall AIS 13.43 SD 9.11) generated effect sizes of 5.67, 9.14, 9.87, and 9.57 decrease in mean overall AIS, respectively, versus the MNT.
Discussion
The presented rat model and scoring system represent the clinical adhesion disease process. hPSC‐based interventions significantly reduce abdominal adhesions in this pilot dataset.</description><subject>Abdomen</subject><subject>Abdominal wall</subject><subject>adhesions</subject><subject>animal model</subject><subject>bowel obstruction</subject><subject>Health services</subject><subject>Ischemia</subject><subject>Mean</subject><subject>Placenta</subject><subject>regenerative medicine</subject><subject>Secretome</subject><subject>Stem cells</subject><subject>Variance analysis</subject><issn>0041-1132</issn><issn>1537-2995</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kctOxCAUhonR6Di68AUMiRtdVKH0Au6M8ZZoNGZcN0w5xBpaKtAx7vQNfEafRMYZXZjI5iz4zsc5_AjtUHJI4zkKTh_SkudiBY1ozsokFSJfRSNCMppQytINtOn9EyEkFYSuow3GC8FIXozQ-52DGXShsR22GvfWh8-3D9uDk6GZAZbqEXy89Mf4xiowWEXc2L6NPVh2CveNsQHbIdS2BT93PA6t7HBvZB0ZabAP0OIajIniqfSgcNMFcMtX_RZa09J42F7WMXo4P5ucXibXtxdXpyfXSc0oEwnPNNdpQZmKa1BJeMY5F1zRWjMhgHBKBAhWS8i11kpkulC6IKrMM5nCtGBjtL_w9s4-D-BD1TZ-PpbswA6-iv9BaFmkeRnRvT_okx1cF6eLVJFykTLOI3WwoGpnvXegq941rXSvFSXVPJcq5lJ95xLZ3aVxmLagfsmfICJwtABeGgOv_5uqyf35QvkFMTqbMA</recordid><startdate>202406</startdate><enddate>202406</enddate><creator>Carmichael, Samuel P.</creator><creator>Chandra, Prafulla K.</creator><creator>Vaughan, John W.</creator><creator>Kline, David M.</creator><creator>Ip, Edward H.</creator><creator>Holcomb, John B.</creator><creator>Atala, Anthony</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0237-4244</orcidid><orcidid>https://orcid.org/0000-0001-8312-9157</orcidid></search><sort><creationdate>202406</creationdate><title>Prevention of post‐operative adhesions: Model development and pilot outcomes of human placental stem cell‐based interventions</title><author>Carmichael, Samuel P. ; Chandra, Prafulla K. ; Vaughan, John W. ; Kline, David M. ; Ip, Edward H. ; Holcomb, John B. ; Atala, Anthony</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3139-84f8f2613d0001a08488898d1cf399e08109e93cae5fffd94f6df60d754a2eb63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Abdomen</topic><topic>Abdominal wall</topic><topic>adhesions</topic><topic>animal model</topic><topic>bowel obstruction</topic><topic>Health services</topic><topic>Ischemia</topic><topic>Mean</topic><topic>Placenta</topic><topic>regenerative medicine</topic><topic>Secretome</topic><topic>Stem cells</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carmichael, Samuel P.</creatorcontrib><creatorcontrib>Chandra, Prafulla K.</creatorcontrib><creatorcontrib>Vaughan, John W.</creatorcontrib><creatorcontrib>Kline, David M.</creatorcontrib><creatorcontrib>Ip, Edward H.</creatorcontrib><creatorcontrib>Holcomb, John B.</creatorcontrib><creatorcontrib>Atala, Anthony</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carmichael, Samuel P.</au><au>Chandra, Prafulla K.</au><au>Vaughan, John W.</au><au>Kline, David M.</au><au>Ip, Edward H.</au><au>Holcomb, John B.</au><au>Atala, Anthony</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of post‐operative adhesions: Model development and pilot outcomes of human placental stem cell‐based interventions</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2024-06</date><risdate>2024</risdate><volume>64</volume><issue>6</issue><spage>1059</spage><epage>1067</epage><pages>1059-1067</pages><issn>0041-1132</issn><issn>1537-2995</issn><eissn>1537-2995</eissn><abstract>Background
Abdominal adhesions are the most common surgical complication and without reliable prophylactics. This study presents a novel rat model for abdominal adhesions and reports pilot results of human placental stem cell (hPSC)‐based therapies.
Methods
Forty‐four (n = 44) male Sprague–Dawley rats (250‐350 g) were used in the experiment. Of these, thirty‐eight (n = 38) were included in a preliminary data set to determine a minimum treatment effect. Adhesions were created in a reproducible model to the abdominal wall and between organs. Experimental groups included the control group (Model No Treatment, MNT), Plasmalyte A (Media Alone, MA, 10 mL), hPSC (5 × 106 cells/10 mL Plasmalyte A), hPSC‐CM (hPSC secretome, conditioned media) in 10 mL Plasmalyte A, Seprafilm™ (Baxter, Deerfield, IL), and sham animals (laparotomy only). Treatments were inserted intraperitoneally (IP) and the study period was 14 days post‐operation. Results are reported as the difference between means of an index statistic (AIS, Animal Index Score) and compared by ANOVA with pairwise comparison.
Results
The overall mean AIS was 23 (SD 6.16) for the MNT group with an average of 75% of ischemic buttons involved in abdominal adhesions. Treatment groups MA (mean overall AIS 17.33 SD 6.4), hPSC (mean overall AIS 13.86 SD 5.01), hPSC‐CM (mean overall AIS 13.13 SD 6.15), and Seprafilm (mean overall AIS 13.43 SD 9.11) generated effect sizes of 5.67, 9.14, 9.87, and 9.57 decrease in mean overall AIS, respectively, versus the MNT.
Discussion
The presented rat model and scoring system represent the clinical adhesion disease process. hPSC‐based interventions significantly reduce abdominal adhesions in this pilot dataset.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>38693056</pmid><doi>10.1111/trf.17859</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0237-4244</orcidid><orcidid>https://orcid.org/0000-0001-8312-9157</orcidid></addata></record> |
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subjects | Abdomen Abdominal wall adhesions animal model bowel obstruction Health services Ischemia Mean Placenta regenerative medicine Secretome Stem cells Variance analysis |
title | Prevention of post‐operative adhesions: Model development and pilot outcomes of human placental stem cell‐based interventions |
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