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Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement
Objectives: The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults an...
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Published in: | Tissue engineering. Part A 2014-03, Vol.20 (5-6), p.13-1011 |
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container_issue | 5-6 |
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container_title | Tissue engineering. Part A |
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creator | Neumann, Anneke Sarikouch, Samir Breymann, Thomas Cebotari, Serghei Boethig, Dietmar Horke, Alexander Beerbaum, Philipp Westhoff-Bleck, Mechthild Bertram, Harald Ono, Masamichi Tudorache, Igor Haverich, Axel Beutel, Gernot |
description | Objectives:
The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults and could potentially avoid significant activation of the immune system, as more than 99% of the donor DNA is removed during the decellularization process. While the humoral immune response to decellularized allografts has been studied, detailed information on the more significant cellular immune response is currently lacking.
Methods and Results:
Peripheral blood samples were obtained from patients undergoing pulmonary valve replacement with DPH before, after, and for approximately 3 years after implantation. Absolute counts and percentages of mature T- (CD3
+
), B- (CD19
+
), and natural killer- (CD16
+
/CD56
+
) cells, as well as T helper- (CD4
+
) and cytotoxic T-cell- (CD8
+
) subsets, were determined by fluorescence-activated cell sorting (FACS). Between May 2009 and September 2013, 199 blood samples taken from 47 patients with a mean age at DPH implantation of 16.6±10.8 years were analyzed. The hemodynamic performance of DPH was excellent in all but one patient, and no valve-related deaths or conduit explantations were observed. The short-term follow up revealed a significant postoperative decrease in cell counts of most subtypes with reconstitution after 3 months. Continued assessment did not show any significant deviations in cell counts from their baseline values.
Conclusion:
The absence of cellular immune response in patients receiving DPH supports the concept that decellularization can provide a basis for autologous regeneration. |
doi_str_mv | 10.1089/ten.tea.2013.0316 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3938920</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1504155932</sourcerecordid><originalsourceid>FETCH-LOGICAL-c622t-4291d288e6ead7b307dbab3463089fad98427edde3a19286ff879cbd9d36d3f03</originalsourceid><addsrcrecordid>eNqNkk2LFDEQhoMo7jr6A7xIwIuXGfPRk3QuwjDu6sKC4hd6CulO9UyWdDKbdA-MP8LfbJpZB_Wih5AieeqtVOVF6CklC0pq9XKAsBjALBihfEE4FffQOVVczjlffr1_iit6hh7lfEOIIELKh-iMVZTXlSTn6MeFSf6APx7yAL1r8Rq8H71J-KrvxwD4A-RdDBmwC3i9dd4mCNgEi7_FMWzwyo5-yIVqwe1dOXhdoqOC-w4WXybIW7zyPm6S6QrZxYTfj76PwaQD_mL8fqqx86aFHsLwGD3ojM_w5G6foc-XF5_Wb-fX795crVfX81YwNswrpqhldQ0CjJUNJ9I2puGV4GUsnbGqrpgEa4Ebqlgtuq6Wqm2sslxY3hE-Q6-Ourux6cG2pXQyXu-S68u7dDRO_3kT3FZv4l5zxWvFJoEXdwIp3o6QB927PLVuAsQxayqk4JWSZPlvdEkqulwqzgr6_C_0Jo4plElMFCelcvm5GaJHqk0x5wTd6d2U6MkYuhijLKMnY-jJGCXn2e8NnzJ-OaEA8ghMxyYE76CBNPyH9E_rSst9</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1503092041</pqid></control><display><type>article</type><title>Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement</title><source>Mary Ann Liebert Online Subscription</source><creator>Neumann, Anneke ; Sarikouch, Samir ; Breymann, Thomas ; Cebotari, Serghei ; Boethig, Dietmar ; Horke, Alexander ; Beerbaum, Philipp ; Westhoff-Bleck, Mechthild ; Bertram, Harald ; Ono, Masamichi ; Tudorache, Igor ; Haverich, Axel ; Beutel, Gernot</creator><creatorcontrib>Neumann, Anneke ; Sarikouch, Samir ; Breymann, Thomas ; Cebotari, Serghei ; Boethig, Dietmar ; Horke, Alexander ; Beerbaum, Philipp ; Westhoff-Bleck, Mechthild ; Bertram, Harald ; Ono, Masamichi ; Tudorache, Igor ; Haverich, Axel ; Beutel, Gernot</creatorcontrib><description>Objectives:
The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults and could potentially avoid significant activation of the immune system, as more than 99% of the donor DNA is removed during the decellularization process. While the humoral immune response to decellularized allografts has been studied, detailed information on the more significant cellular immune response is currently lacking.
Methods and Results:
Peripheral blood samples were obtained from patients undergoing pulmonary valve replacement with DPH before, after, and for approximately 3 years after implantation. Absolute counts and percentages of mature T- (CD3
+
), B- (CD19
+
), and natural killer- (CD16
+
/CD56
+
) cells, as well as T helper- (CD4
+
) and cytotoxic T-cell- (CD8
+
) subsets, were determined by fluorescence-activated cell sorting (FACS). Between May 2009 and September 2013, 199 blood samples taken from 47 patients with a mean age at DPH implantation of 16.6±10.8 years were analyzed. The hemodynamic performance of DPH was excellent in all but one patient, and no valve-related deaths or conduit explantations were observed. The short-term follow up revealed a significant postoperative decrease in cell counts of most subtypes with reconstitution after 3 months. Continued assessment did not show any significant deviations in cell counts from their baseline values.
Conclusion:
The absence of cellular immune response in patients receiving DPH supports the concept that decellularization can provide a basis for autologous regeneration.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><identifier>DOI: 10.1089/ten.tea.2013.0316</identifier><identifier>PMID: 24138470</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Adolescent ; Allografts - immunology ; Allografts - transplantation ; Cellular biology ; Child ; Children & youth ; Cohort Studies ; Female ; Follow-Up Studies ; Hemodynamics ; Humans ; Immunity, Cellular - immunology ; Male ; Original ; Original Articles ; Pulmonary arteries ; Pulmonary Valve - immunology ; Pulmonary Valve - transplantation ; Skin & tissue grafts ; Young Adult ; Young adults</subject><ispartof>Tissue engineering. Part A, 2014-03, Vol.20 (5-6), p.13-1011</ispartof><rights>2014, Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2014, Mary Ann Liebert, Inc.</rights><rights>Copyright 2014, Mary Ann Liebert, Inc. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c622t-4291d288e6ead7b307dbab3463089fad98427edde3a19286ff879cbd9d36d3f03</citedby><cites>FETCH-LOGICAL-c622t-4291d288e6ead7b307dbab3463089fad98427edde3a19286ff879cbd9d36d3f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/ten.tea.2013.0316$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/ten.tea.2013.0316$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>230,314,780,784,885,3040,21721,27922,27923,55289,55301</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24138470$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neumann, Anneke</creatorcontrib><creatorcontrib>Sarikouch, Samir</creatorcontrib><creatorcontrib>Breymann, Thomas</creatorcontrib><creatorcontrib>Cebotari, Serghei</creatorcontrib><creatorcontrib>Boethig, Dietmar</creatorcontrib><creatorcontrib>Horke, Alexander</creatorcontrib><creatorcontrib>Beerbaum, Philipp</creatorcontrib><creatorcontrib>Westhoff-Bleck, Mechthild</creatorcontrib><creatorcontrib>Bertram, Harald</creatorcontrib><creatorcontrib>Ono, Masamichi</creatorcontrib><creatorcontrib>Tudorache, Igor</creatorcontrib><creatorcontrib>Haverich, Axel</creatorcontrib><creatorcontrib>Beutel, Gernot</creatorcontrib><title>Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement</title><title>Tissue engineering. Part A</title><addtitle>Tissue Eng Part A</addtitle><description>Objectives:
The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults and could potentially avoid significant activation of the immune system, as more than 99% of the donor DNA is removed during the decellularization process. While the humoral immune response to decellularized allografts has been studied, detailed information on the more significant cellular immune response is currently lacking.
Methods and Results:
Peripheral blood samples were obtained from patients undergoing pulmonary valve replacement with DPH before, after, and for approximately 3 years after implantation. Absolute counts and percentages of mature T- (CD3
+
), B- (CD19
+
), and natural killer- (CD16
+
/CD56
+
) cells, as well as T helper- (CD4
+
) and cytotoxic T-cell- (CD8
+
) subsets, were determined by fluorescence-activated cell sorting (FACS). Between May 2009 and September 2013, 199 blood samples taken from 47 patients with a mean age at DPH implantation of 16.6±10.8 years were analyzed. The hemodynamic performance of DPH was excellent in all but one patient, and no valve-related deaths or conduit explantations were observed. The short-term follow up revealed a significant postoperative decrease in cell counts of most subtypes with reconstitution after 3 months. Continued assessment did not show any significant deviations in cell counts from their baseline values.
Conclusion:
The absence of cellular immune response in patients receiving DPH supports the concept that decellularization can provide a basis for autologous regeneration.</description><subject>Adolescent</subject><subject>Allografts - immunology</subject><subject>Allografts - transplantation</subject><subject>Cellular biology</subject><subject>Child</subject><subject>Children & youth</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Immunity, Cellular - immunology</subject><subject>Male</subject><subject>Original</subject><subject>Original Articles</subject><subject>Pulmonary arteries</subject><subject>Pulmonary Valve - immunology</subject><subject>Pulmonary Valve - transplantation</subject><subject>Skin & tissue grafts</subject><subject>Young Adult</subject><subject>Young adults</subject><issn>1937-3341</issn><issn>1937-335X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkk2LFDEQhoMo7jr6A7xIwIuXGfPRk3QuwjDu6sKC4hd6CulO9UyWdDKbdA-MP8LfbJpZB_Wih5AieeqtVOVF6CklC0pq9XKAsBjALBihfEE4FffQOVVczjlffr1_iit6hh7lfEOIIELKh-iMVZTXlSTn6MeFSf6APx7yAL1r8Rq8H71J-KrvxwD4A-RdDBmwC3i9dd4mCNgEi7_FMWzwyo5-yIVqwe1dOXhdoqOC-w4WXybIW7zyPm6S6QrZxYTfj76PwaQD_mL8fqqx86aFHsLwGD3ojM_w5G6foc-XF5_Wb-fX795crVfX81YwNswrpqhldQ0CjJUNJ9I2puGV4GUsnbGqrpgEa4Ebqlgtuq6Wqm2sslxY3hE-Q6-Ourux6cG2pXQyXu-S68u7dDRO_3kT3FZv4l5zxWvFJoEXdwIp3o6QB927PLVuAsQxayqk4JWSZPlvdEkqulwqzgr6_C_0Jo4plElMFCelcvm5GaJHqk0x5wTd6d2U6MkYuhijLKMnY-jJGCXn2e8NnzJ-OaEA8ghMxyYE76CBNPyH9E_rSst9</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Neumann, Anneke</creator><creator>Sarikouch, Samir</creator><creator>Breymann, Thomas</creator><creator>Cebotari, Serghei</creator><creator>Boethig, Dietmar</creator><creator>Horke, Alexander</creator><creator>Beerbaum, Philipp</creator><creator>Westhoff-Bleck, Mechthild</creator><creator>Bertram, Harald</creator><creator>Ono, Masamichi</creator><creator>Tudorache, Igor</creator><creator>Haverich, Axel</creator><creator>Beutel, Gernot</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20140301</creationdate><title>Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement</title><author>Neumann, Anneke ; Sarikouch, Samir ; Breymann, Thomas ; Cebotari, Serghei ; Boethig, Dietmar ; Horke, Alexander ; Beerbaum, Philipp ; Westhoff-Bleck, Mechthild ; Bertram, Harald ; Ono, Masamichi ; Tudorache, Igor ; Haverich, Axel ; Beutel, Gernot</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c622t-4291d288e6ead7b307dbab3463089fad98427edde3a19286ff879cbd9d36d3f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Allografts - immunology</topic><topic>Allografts - transplantation</topic><topic>Cellular biology</topic><topic>Child</topic><topic>Children & youth</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Immunity, Cellular - immunology</topic><topic>Male</topic><topic>Original</topic><topic>Original Articles</topic><topic>Pulmonary arteries</topic><topic>Pulmonary Valve - immunology</topic><topic>Pulmonary Valve - transplantation</topic><topic>Skin & tissue grafts</topic><topic>Young Adult</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neumann, Anneke</creatorcontrib><creatorcontrib>Sarikouch, Samir</creatorcontrib><creatorcontrib>Breymann, Thomas</creatorcontrib><creatorcontrib>Cebotari, Serghei</creatorcontrib><creatorcontrib>Boethig, Dietmar</creatorcontrib><creatorcontrib>Horke, Alexander</creatorcontrib><creatorcontrib>Beerbaum, Philipp</creatorcontrib><creatorcontrib>Westhoff-Bleck, Mechthild</creatorcontrib><creatorcontrib>Bertram, Harald</creatorcontrib><creatorcontrib>Ono, Masamichi</creatorcontrib><creatorcontrib>Tudorache, Igor</creatorcontrib><creatorcontrib>Haverich, Axel</creatorcontrib><creatorcontrib>Beutel, Gernot</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</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 Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science 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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Tissue engineering. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neumann, Anneke</au><au>Sarikouch, Samir</au><au>Breymann, Thomas</au><au>Cebotari, Serghei</au><au>Boethig, Dietmar</au><au>Horke, Alexander</au><au>Beerbaum, Philipp</au><au>Westhoff-Bleck, Mechthild</au><au>Bertram, Harald</au><au>Ono, Masamichi</au><au>Tudorache, Igor</au><au>Haverich, Axel</au><au>Beutel, Gernot</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement</atitle><jtitle>Tissue engineering. Part A</jtitle><addtitle>Tissue Eng Part A</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>20</volume><issue>5-6</issue><spage>13</spage><epage>1011</epage><pages>13-1011</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Objectives:
The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults and could potentially avoid significant activation of the immune system, as more than 99% of the donor DNA is removed during the decellularization process. While the humoral immune response to decellularized allografts has been studied, detailed information on the more significant cellular immune response is currently lacking.
Methods and Results:
Peripheral blood samples were obtained from patients undergoing pulmonary valve replacement with DPH before, after, and for approximately 3 years after implantation. Absolute counts and percentages of mature T- (CD3
+
), B- (CD19
+
), and natural killer- (CD16
+
/CD56
+
) cells, as well as T helper- (CD4
+
) and cytotoxic T-cell- (CD8
+
) subsets, were determined by fluorescence-activated cell sorting (FACS). Between May 2009 and September 2013, 199 blood samples taken from 47 patients with a mean age at DPH implantation of 16.6±10.8 years were analyzed. The hemodynamic performance of DPH was excellent in all but one patient, and no valve-related deaths or conduit explantations were observed. The short-term follow up revealed a significant postoperative decrease in cell counts of most subtypes with reconstitution after 3 months. Continued assessment did not show any significant deviations in cell counts from their baseline values.
Conclusion:
The absence of cellular immune response in patients receiving DPH supports the concept that decellularization can provide a basis for autologous regeneration.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>24138470</pmid><doi>10.1089/ten.tea.2013.0316</doi><tpages>999</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Tissue engineering. Part A, 2014-03, Vol.20 (5-6), p.13-1011 |
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language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3938920 |
source | Mary Ann Liebert Online Subscription |
subjects | Adolescent Allografts - immunology Allografts - transplantation Cellular biology Child Children & youth Cohort Studies Female Follow-Up Studies Hemodynamics Humans Immunity, Cellular - immunology Male Original Original Articles Pulmonary arteries Pulmonary Valve - immunology Pulmonary Valve - transplantation Skin & tissue grafts Young Adult Young adults |
title | Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement |
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