<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(12)</volume><submitter>Denlinger N</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Chimeric antigen receptor (CAR) T-cell therapy has revolutionized treatment for relapsed/refractory B-cell non-Hodgkin lymphoma (NHL). Robust biomarkers and a complete understanding of CAR T-cell function in the postinfusion phase remain limited. Here, we used a 37-color spectral flow cytometry panel to perform high dimensional single-cell analysis of postinfusion samples in 26 patients treated with CD28 costimulatory domain containing commercial CAR T cells for NHL and focused on computationally gated CD8+ CAR T cells. We found that the presence of postinfusion Programmed cell death protein 1 (PD-1)+ CD8+ CAR T cells at the day 14 time point highly correlated with the ability to achieve complete response (CR) by 6 months. Further analysis identified multiple subtypes of C</pubmed_abstract><journal>Blood advances</journal><pagination>3140-3153</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11222947</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Postinfusion PD-1+ CD8+ CAR T cells identify patients responsive to CD19 CAR T-cell therapy in non-Hodgkin lymphoma.</pubmed_title><pmcid>PMC11222947</pmcid><pubmed_authors>Chan WK</pubmed_authors><pubmed_authors>Jaglowski S</pubmed_authors><pubmed_authors>Baiocchi RA</pubmed_authors><pubmed_authors>Song NJ</pubmed_authors><pubmed_authors>Wu D</pubmed_authors><pubmed_authors>Voorhees TJ</pubmed_authors><pubmed_authors>Miao J</pubmed_authors><pubmed_authors>Reneau JC</pubmed_authors><pubmed_authors>Reynolds K</pubmed_authors><pubmed_authors>Epperla N</pubmed_authors><pubmed_authors>Sawalha Y</pubmed_authors><pubmed_authors>Rubinstein MP</pubmed_authors><pubmed_authors>Hanel W</pubmed_authors><pubmed_authors>Kittai AS</pubmed_authors><pubmed_authors>de Lima M</pubmed_authors><pubmed_authors>Alinari L</pubmed_authors><pubmed_authors>Bond DA</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Denlinger N</pubmed_authors><pubmed_authors>Sigmund A</pubmed_authors><pubmed_authors>Christian B</pubmed_authors><pubmed_authors>Maddocks K</pubmed_authors><pubmed_authors>Peterson C</pubmed_authors><pubmed_authors>Song C</pubmed_authors><pubmed_authors>Jeon H</pubmed_authors><pubmed_authors>Vasu S</pubmed_authors><pubmed_authors>Bolz RM</pubmed_authors><pubmed_authors>Bezerra E</pubmed_authors><pubmed_authors>Chung D</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Brammer J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Postinfusion PD-1+ CD8+ CAR T cells identify patients responsive to CD19 CAR T-cell therapy in non-Hodgkin lymphoma.</name><description>&lt;h4>Abstract&lt;/h4>Chimeric antigen receptor (CAR) T-cell therapy has revolutionized treatment for relapsed/refractory B-cell non-Hodgkin lymphoma (NHL). Robust biomarkers and a complete understanding of CAR T-cell function in the postinfusion phase remain limited. Here, we used a 37-color spectral flow cytometry panel to perform high dimensional single-cell analysis of postinfusion samples in 26 patients treated with CD28 costimulatory domain containing commercial CAR T cells for NHL and focused on computationally gated CD8+ CAR T cells. We found that the presence of postinfusion Programmed cell death protein 1 (PD-1)+ CD8+ CAR T cells at the day 14 time point highly correlated with the ability to achieve complete response (CR) by 6 months. Further analysis identified multiple subtypes of C</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-04-04T19:23:27.185Z</modification><creation>2025-04-04T19:23:27.185Z</creation></dates><accession>S-EPMC11222947</accession><cross_references><pubmed>38607381</pubmed><doi>10.1182/bloodadvances.2023012073</doi></cross_references></HashMap>