<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ahlenstiel-Grunow T</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>Novartis</funding><pagination>502-516</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8054884</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Pharmacokinetic monitoring is insufficient to estimate the intensity of immunosuppression after transplantation. Virus-specific T cells correlate with both virus-specific and general cellular immune defense. Additional steering of immunosuppressive therapy by virus-specific T cell levels might optimize dosing of immunosuppressants.&lt;h4>Methods&lt;/h4>In a multicenter, randomized, controlled trial, we randomized 64 pediatric kidney recipients to a control group with trough-level monitoring of immunosuppressants or to an intervention group with additional steering of immunosuppressive therapy by levels of virus-specific T cells (quantified by cytokine flow cytometry). Both groups received immunosuppression with cyclosporin A and everolimus in the same target range of trough le</pubmed_abstract><journal>Journal of the American Society of Nephrology : JASN</journal><pubmed_title>Steering Transplant Immunosuppression by Measuring Virus-Specific T Cell Levels: The Randomized, Controlled IVIST Trial.</pubmed_title><pmcid>PMC8054884</pmcid><funding_grant_id>01EO0802</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Großhennig A</pubmed_authors><pubmed_authors>Staude H</pubmed_authors><pubmed_authors>Sabau R</pubmed_authors><pubmed_authors>Oh J</pubmed_authors><pubmed_authors>Schild R</pubmed_authors><pubmed_authors>Taylan C</pubmed_authors><pubmed_authors>Weber LT</pubmed_authors><pubmed_authors>Pape L</pubmed_authors><pubmed_authors>Ahlenstiel-Grunow T</pubmed_authors><pubmed_authors>Verboom M</pubmed_authors><pubmed_authors>Schroder C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Steering Transplant Immunosuppression by Measuring Virus-Specific T Cell Levels: The Randomized, Controlled IVIST Trial.</name><description>&lt;h4>Background&lt;/h4>Pharmacokinetic monitoring is insufficient to estimate the intensity of immunosuppression after transplantation. Virus-specific T cells correlate with both virus-specific and general cellular immune defense. Additional steering of immunosuppressive therapy by virus-specific T cell levels might optimize dosing of immunosuppressants.&lt;h4>Methods&lt;/h4>In a multicenter, randomized, controlled trial, we randomized 64 pediatric kidney recipients to a control group with trough-level monitoring of immunosuppressants or to an intervention group with additional steering of immunosuppressive therapy by levels of virus-specific T cells (quantified by cytokine flow cytometry). Both groups received immunosuppression with cyclosporin A and everolimus in the same target range of trough le</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-04-29T10:10:53.495Z</modification><creation>2022-02-11T15:44:01.696Z</creation></dates><accession>S-EPMC8054884</accession><cross_references><pubmed>33323473</pubmed><doi>10.1681/asn.2020050645</doi><doi>10.1681/ASN.2020050645</doi></cross_references></HashMap>