<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(5)</volume><submitter>Ramm R</submitter><funding>German Research Foundation</funding><funding>Deutsche Herzstiftung e. V.</funding><pubmed_abstract>Decellularization of xenogeneic heart valves might lead to excellent regenerative implants, from which many patients could benefit. However, this material carries various xenogeneic epitopes and thus bears a considerable inherent immunological risk. Here, we investigated the regenerative and immunogenic potential of xenogeneic decellularized heart valve implants using pigs deficient for the galactosyltransferase gene (GGTA1-KO) as novel large animal model. Decellularized aortic and pulmonary heart valves obtained from sheep, wild-type pigs or GGTA1-KO pigs were implanted into GGTA1-KO pigs for 3, or 6 months, respectively. Explants were analyzed histologically, immunhistologically (CD3, CD21 and CD172a) and anti-αGal antibody serum titers were determined by ELISA. Xenogeneic sheep derived </pubmed_abstract><journal>Regenerative biomaterials</journal><pagination>rbab036</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8329474</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunological and functional features of decellularized xenogeneic heart valves after transplantation into GGTA1-KO pigs.</pubmed_title><pmcid>PMC8329474</pmcid><pubmed_authors>Kohler P</pubmed_authors><pubmed_authors>Tudorache I</pubmed_authors><pubmed_authors>Ciubotaru A</pubmed_authors><pubmed_authors>Petersen B</pubmed_authors><pubmed_authors>Hoffler K</pubmed_authors><pubmed_authors>Goecke T</pubmed_authors><pubmed_authors>Haverich A</pubmed_authors><pubmed_authors>Bothe F</pubmed_authors><pubmed_authors>Niemann H</pubmed_authors><pubmed_authors>Ramm R</pubmed_authors><pubmed_authors>Sarikouch S</pubmed_authors><pubmed_authors>Cebotari S</pubmed_authors><pubmed_authors>Hilfiker A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunological and functional features of decellularized xenogeneic heart valves after transplantation into GGTA1-KO pigs.</name><description>Decellularization of xenogeneic heart valves might lead to excellent regenerative implants, from which many patients could benefit. However, this material carries various xenogeneic epitopes and thus bears a considerable inherent immunological risk. Here, we investigated the regenerative and immunogenic potential of xenogeneic decellularized heart valve implants using pigs deficient for the galactosyltransferase gene (GGTA1-KO) as novel large animal model. Decellularized aortic and pulmonary heart valves obtained from sheep, wild-type pigs or GGTA1-KO pigs were implanted into GGTA1-KO pigs for 3, or 6 months, respectively. Explants were analyzed histologically, immunhistologically (CD3, CD21 and CD172a) and anti-αGal antibody serum titers were determined by ELISA. Xenogeneic sheep derived </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-06-01T03:29:35.083Z</modification><creation>2024-11-15T21:38:02.711Z</creation></dates><accession>S-EPMC8329474</accession><cross_references><pubmed>35928180</pubmed><doi>10.1093/rb/rbab036</doi></cross_references></HashMap>