<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mai Q</submitter><funding>Guangdong Key Laboratory of Immune Regulation and Immunotherapy</funding><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>Guangdong Natural Science Foundation Outstanding Youth Project</funding><pagination>85</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11334566</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Epstein-Barr virus (EBV) related post-transplant lymphoproliferative disorder (EBV-PTLD) is a life-threatening complication after hematopoietic stem cell transplantation (HSCT) or solid organ transplantation (SOT), for which no standard therapeutic means have been developed. Significant increase expression of natural killer group 2 member D ligands (NKG2DLs) was observed on B-lymphoblastoid cells of EBV-PTLD, indicating NKG2DLs as potential therapeutic targets for treatment of EBV-PTLD. In this study, the recombinant constructs of NKG2D CAR and IL-15/IL-15Rα-NKG2D CAR were generated with a retroviral vector and then transduced to human T cells to produce NKG2D CAR-T and IL-15/IL-15Rα-NKG2D CAR-T cells, respectively. B-lymphoblastoid cell lines (B-LCLs) and the xenografted mouse models were</pubmed_abstract><journal>Experimental hematology &amp; oncology</journal><pubmed_title>Efficacy of NKG2D CAR-T cells with IL-15/IL-15Rα signaling for treating Epstein-Barr virus-associated lymphoproliferative disorder.</pubmed_title><pmcid>PMC11334566</pmcid><funding_grant_id>2022B1515020050</funding_grant_id><funding_grant_id>2022A1515110828</funding_grant_id><funding_grant_id>82300252</funding_grant_id><funding_grant_id>2023A1515110236</funding_grant_id><funding_grant_id>2022B1212010009</funding_grant_id><pubmed_authors>Deng S</pubmed_authors><pubmed_authors>Zeng Q</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Fu Y</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Mai Q</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Pang Y</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Zeng J</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>He B</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy of NKG2D CAR-T cells with IL-15/IL-15Rα signaling for treating Epstein-Barr virus-associated lymphoproliferative disorder.</name><description>Epstein-Barr virus (EBV) related post-transplant lymphoproliferative disorder (EBV-PTLD) is a life-threatening complication after hematopoietic stem cell transplantation (HSCT) or solid organ transplantation (SOT), for which no standard therapeutic means have been developed. Significant increase expression of natural killer group 2 member D ligands (NKG2DLs) was observed on B-lymphoblastoid cells of EBV-PTLD, indicating NKG2DLs as potential therapeutic targets for treatment of EBV-PTLD. In this study, the recombinant constructs of NKG2D CAR and IL-15/IL-15Rα-NKG2D CAR were generated with a retroviral vector and then transduced to human T cells to produce NKG2D CAR-T and IL-15/IL-15Rα-NKG2D CAR-T cells, respectively. B-lymphoblastoid cell lines (B-LCLs) and the xenografted mouse models were</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-07-15T08:03:57.288Z</modification><creation>2025-04-05T21:20:43.079Z</creation></dates><accession>S-EPMC11334566</accession><cross_references><pubmed>39160631</pubmed><doi>10.1186/s40164-024-00553-z</doi></cross_references></HashMap>