<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Zhao J</submitter><pubmed_abstract>Allograft rejection has been an obstacle for the long-term survival of patients. CD70, a tumor necrosis factor (TNF) family member critically expressed on antigen-presenting cells and strongly but transiently up-regulated during lymphocyte activation, represents an important co-stimulatory molecule that induces effective T cell responses. We used a mouse heterotopic cardiac transplantation model to evaluate the effects of monotherapy with the antibody targeting mouse CD70 (FR70) on transplantation tolerance and its immunoregulatory activity. FR70-treated C3H recipient mice permanently accepted B6 fully mismatched cardiac allografts. Consistent with the graft survival, the infiltration of CD8&lt;sup>+&lt;/sup> T cells in the graft was reduced, dendritic cells were differentiated into a tolerogeni</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>555996</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7961176</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Monotherapy With Anti-CD70 Antibody Causes Long-Term Mouse Cardiac Allograft Acceptance With Induction of Tolerogenic Dendritic Cells.</pubmed_title><pmcid>PMC7961176</pmcid><pubmed_authors>Nonomura N</pubmed_authors><pubmed_authors>Zabrocki P</pubmed_authors><pubmed_authors>Que W</pubmed_authors><pubmed_authors>Fujino M</pubmed_authors><pubmed_authors>Ueta H</pubmed_authors><pubmed_authors>Du X</pubmed_authors><pubmed_authors>Guo WZ</pubmed_authors><pubmed_authors>Li XK</pubmed_authors><pubmed_authors>de Haard H</pubmed_authors><pubmed_authors>Tokuda N</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Ichimaru N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Monotherapy With Anti-CD70 Antibody Causes Long-Term Mouse Cardiac Allograft Acceptance With Induction of Tolerogenic Dendritic Cells.</name><description>Allograft rejection has been an obstacle for the long-term survival of patients. CD70, a tumor necrosis factor (TNF) family member critically expressed on antigen-presenting cells and strongly but transiently up-regulated during lymphocyte activation, represents an important co-stimulatory molecule that induces effective T cell responses. We used a mouse heterotopic cardiac transplantation model to evaluate the effects of monotherapy with the antibody targeting mouse CD70 (FR70) on transplantation tolerance and its immunoregulatory activity. FR70-treated C3H recipient mice permanently accepted B6 fully mismatched cardiac allografts. Consistent with the graft survival, the infiltration of CD8&lt;sup>+&lt;/sup> T cells in the graft was reduced, dendritic cells were differentiated into a tolerogeni</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-21T17:00:57.659Z</modification><creation>2025-04-21T17:00:57.659Z</creation></dates><accession>S-EPMC7961176</accession><cross_references><pubmed>33737923</pubmed><doi>10.3389/fimmu.2020.555996</doi></cross_references></HashMap>