<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li Y</submitter><funding>Shanghai Clinical Medical Research Center Project</funding><funding>Shanghai Agriculture Applied Technology Development Program Project</funding><funding>NSFC</funding><funding>Shanghai Municipal Education Commission Project</funding><funding>National Natural Science Foundation of China</funding><funding>Ministry of Science and Technology of China Project</funding><funding>Shanghai Municipal Health Commission Project</funding><funding>Shanghai Municipal Science and Technology Project</funding><funding>National Innovation Special Zone Project</funding><funding>Shanghai Jiao Tong University Projects</funding><pagination>e629</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8574956</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(11)</volume><pubmed_abstract>Tacrolimus (FK506) and rapamycin (RAPA) are widely used to maintain long-term immunosuppression after organ transplantation. However, the impact of accumulative drug administration on the recipients' immune systems remains unclear. We investigated the impact of 3-year FK506 or RAPA treatment after renal transplantation on the human immune systems. A discovery cohort of 30 patients was first recruited, and we discovered two distinctive T lineage suppressive regulatory patterns induced by chronic treatment of FK506 and RAPA. The increased percentage of senescent CD8&lt;sup>+&lt;/sup> CD57&lt;sup>+&lt;/sup> T lineages and less responsive T cell receptor (TCR) pathway in the FK506 group indicate better graft acceptance. Meanwhile, percentages of regulatory T cells (Tregs) and expression of CTLA-4 were bot</pubmed_abstract><journal>Clinical and translational medicine</journal><pubmed_title>Deep phenotyping of T cell populations under long-term treatment of tacrolimus and rapamycin in patients receiving renal transplantations by mass cytometry.</pubmed_title><pmcid>PMC8574956</pmcid><funding_grant_id>18430760500</funding_grant_id><funding_grant_id>81902587</funding_grant_id><funding_grant_id>2020 SJTU-HUJI</funding_grant_id><funding_grant_id>2017ZX10203205-006-002</funding_grant_id><funding_grant_id>G20180101</funding_grant_id><funding_grant_id>19X190020154</funding_grant_id><funding_grant_id>ZH2018QNA49</funding_grant_id><funding_grant_id>ZH2018QNA54</funding_grant_id><funding_grant_id>SD0820016</funding_grant_id><funding_grant_id>19MC1910800</funding_grant_id><funding_grant_id>ZXWF082101</funding_grant_id><funding_grant_id>YG2016MS60</funding_grant_id><funding_grant_id>Agri-X20200101</funding_grant_id><funding_grant_id>SL2020MS026</funding_grant_id><funding_grant_id>YG2016QN24</funding_grant_id><funding_grant_id>017SHZDZX01</funding_grant_id><funding_grant_id>22077079</funding_grant_id><funding_grant_id>2019CXJQ03</funding_grant_id><funding_grant_id>ZH2018ZDA01</funding_grant_id><funding_grant_id>81871448</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Ding X</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Zhou P</pubmed_authors><pubmed_authors>Jiang H</pubmed_authors><pubmed_authors>An H</pubmed_authors><pubmed_authors>Shen C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deep phenotyping of T cell populations under long-term treatment of tacrolimus and rapamycin in patients receiving renal transplantations by mass cytometry.</name><description>Tacrolimus (FK506) and rapamycin (RAPA) are widely used to maintain long-term immunosuppression after organ transplantation. However, the impact of accumulative drug administration on the recipients' immune systems remains unclear. We investigated the impact of 3-year FK506 or RAPA treatment after renal transplantation on the human immune systems. A discovery cohort of 30 patients was first recruited, and we discovered two distinctive T lineage suppressive regulatory patterns induced by chronic treatment of FK506 and RAPA. The increased percentage of senescent CD8&lt;sup>+&lt;/sup> CD57&lt;sup>+&lt;/sup> T lineages and less responsive T cell receptor (TCR) pathway in the FK506 group indicate better graft acceptance. Meanwhile, percentages of regulatory T cells (Tregs) and expression of CTLA-4 were bot</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-08T20:31:21.326Z</modification><creation>2022-02-11T13:28:48.861Z</creation></dates><accession>S-EPMC8574956</accession><cross_references><pubmed>34841735</pubmed><doi>10.1002/ctm2.629</doi></cross_references></HashMap>