{"title":"Research Progress of T Cell Metabolism in Graft-Versus-Host Disease.","authors":"Yihan Ding, Bo Hu, Chengwan Zhang","doi":"10.1016/j.jtct.2026.10.010","DOIUrl":null,"url":null,"abstract":"<p><p>Graft-versus-host disease (GVHD) is a common and severe complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT). It is caused by activated alloreactive T cells that attack recipient target organs and represents a major cause of non-relapse mortality, thereby limiting the efficacy of allo-HSCT. Persistent alloantigen stimulation can induce metabolic dysregulation in T cells, involving pathways such as glycolysis, lipid metabolism, amino acid metabolism, nucleotide metabolism, and mitochondrial oxidative phosphorylation. Given the close relationship between T cell metabolism and T cell activation, differentiation, and effector functions, targeted modulation of T cell metabolism may emerge as a novel strategy for the prevention and treatment of GVHD. This review summarizes the roles of major T cell metabolic pathways in the pathogenesis and progression of GVHD with the aim of informing future mechanistic studies and therapeutic strategies.</p>","PeriodicalId":23283,"journal":{"name":"Transplantation and Cellular Therapy","volume":" ","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation and Cellular Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jtct.2026.10.010","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Graft-versus-host disease (GVHD) is a common and severe complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT). It is caused by activated alloreactive T cells that attack recipient target organs and represents a major cause of non-relapse mortality, thereby limiting the efficacy of allo-HSCT. Persistent alloantigen stimulation can induce metabolic dysregulation in T cells, involving pathways such as glycolysis, lipid metabolism, amino acid metabolism, nucleotide metabolism, and mitochondrial oxidative phosphorylation. Given the close relationship between T cell metabolism and T cell activation, differentiation, and effector functions, targeted modulation of T cell metabolism may emerge as a novel strategy for the prevention and treatment of GVHD. This review summarizes the roles of major T cell metabolic pathways in the pathogenesis and progression of GVHD with the aim of informing future mechanistic studies and therapeutic strategies.