<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(23)</volume><submitter>Huang Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Transmethylation reactions play an important role on lymphocyte activation and function. S-adenosyl-L-homocysteine hydrolase (SAHH) inhibitors prevent the feedback of transmethylation reactions by S-adenosyl-L-homocysteine (SAH) accumulation, a competitive antagonist of S-adenosylmethionine (SAM)-dependent methyltransferases. However, the role of SAH in solid organ transplantation is currently unclear.&lt;h4>Methods&lt;/h4>A murine model of cardiac transplantation (BALB/C to C57B/6) was established to assess allograft survival, histology, and T cell infiltration. The reversible SAHH inhibitor, DZ2002, and irreversible SAHH inhibitor, adenosine dialdehyde (AdOx), were used to assess their immunosuppressive effects in murine cardiac transplantation, compared with mice with DMSO.</pubmed_abstract><journal>Annals of translational medicine</journal><pagination>1582</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7791210</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Inhibition of S-adenosyl-L-homocysteine hydrolase alleviates alloimmune response by down-regulating CD4&lt;sup>+&lt;/sup> T-cell activation in a mouse heart transplantation model.</pubmed_title><pmcid>PMC7791210</pmcid><pubmed_authors>Ding X</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Du X</pubmed_authors><pubmed_authors>Wang G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibition of S-adenosyl-L-homocysteine hydrolase alleviates alloimmune response by down-regulating CD4&lt;sup>+&lt;/sup> T-cell activation in a mouse heart transplantation model.</name><description>&lt;h4>Background&lt;/h4>Transmethylation reactions play an important role on lymphocyte activation and function. S-adenosyl-L-homocysteine hydrolase (SAHH) inhibitors prevent the feedback of transmethylation reactions by S-adenosyl-L-homocysteine (SAH) accumulation, a competitive antagonist of S-adenosylmethionine (SAM)-dependent methyltransferases. However, the role of SAH in solid organ transplantation is currently unclear.&lt;h4>Methods&lt;/h4>A murine model of cardiac transplantation (BALB/C to C57B/6) was established to assess allograft survival, histology, and T cell infiltration. The reversible SAHH inhibitor, DZ2002, and irreversible SAHH inhibitor, adenosine dialdehyde (AdOx), were used to assess their immunosuppressive effects in murine cardiac transplantation, compared with mice with DMSO.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-05T16:07:06.05Z</modification><creation>2025-04-05T16:07:06.05Z</creation></dates><accession>S-EPMC7791210</accession><cross_references><pubmed>33437781</pubmed><doi>10.21037/atm-20-2899</doi></cross_references></HashMap>