<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Campodonico E</submitter><pubmed_abstract>Hemophagocytic lymphohistiocytosis (HLH) is a hyper-inflammatory syndrome characterized by deficient NK-cell activity, cytokine storm and altered T-cell immunity, potentially sustained by multiple triggers. Recently, a hyperinflammatory condition resembling HLH has emerged as a potential complication of CAR T-cells. HLH represents a diagnostic conundrum due to its rarity, non-specific presentation and lack of validated biomarkers. We investigated a panel of serum cytokines which represent candidate markers to diagnose HLH after CAR-T. We analyzed 2 patients affected by B-cell lymphomas who received anti-CD19 CAR-T and developed HLH defined according to multiple diagnostic criteria. We identified four controls who did not develop HLH: one with CRS without cytopenia, one with cytopenia with </pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1635062</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12390792</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Biomarkers for an early diagnosis of immune effector cell associated-hemophagocytic syndrome.</pubmed_title><pmcid>PMC12390792</pmcid><pubmed_authors>Lupo Stanghellini MT</pubmed_authors><pubmed_authors>Ruggeri A</pubmed_authors><pubmed_authors>Angelillo P</pubmed_authors><pubmed_authors>Noviello M</pubmed_authors><pubmed_authors>Doglio M</pubmed_authors><pubmed_authors>Carrabba MG</pubmed_authors><pubmed_authors>Bruno A</pubmed_authors><pubmed_authors>Pedica F</pubmed_authors><pubmed_authors>Bergonzi GM</pubmed_authors><pubmed_authors>Peccatori J</pubmed_authors><pubmed_authors>Ciceri F</pubmed_authors><pubmed_authors>Diral E</pubmed_authors><pubmed_authors>Corti C</pubmed_authors><pubmed_authors>Ferreri AJM</pubmed_authors><pubmed_authors>Bonini C</pubmed_authors><pubmed_authors>Greco R</pubmed_authors><pubmed_authors>Campodonico E</pubmed_authors><pubmed_authors>Lazzari L</pubmed_authors><pubmed_authors>Ugolini A</pubmed_authors><pubmed_authors>Tassi E</pubmed_authors><pubmed_authors>Ponzoni M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biomarkers for an early diagnosis of immune effector cell associated-hemophagocytic syndrome.</name><description>Hemophagocytic lymphohistiocytosis (HLH) is a hyper-inflammatory syndrome characterized by deficient NK-cell activity, cytokine storm and altered T-cell immunity, potentially sustained by multiple triggers. Recently, a hyperinflammatory condition resembling HLH has emerged as a potential complication of CAR T-cells. HLH represents a diagnostic conundrum due to its rarity, non-specific presentation and lack of validated biomarkers. We investigated a panel of serum cytokines which represent candidate markers to diagnose HLH after CAR-T. We analyzed 2 patients affected by B-cell lymphomas who received anti-CD19 CAR-T and developed HLH defined according to multiple diagnostic criteria. We identified four controls who did not develop HLH: one with CRS without cytopenia, one with cytopenia with </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-05-29T15:15:45.067Z</modification><creation>2026-04-08T05:12:12.67Z</creation></dates><accession>S-EPMC12390792</accession><cross_references><pubmed>40895549</pubmed><doi>10.3389/fimmu.2025.1635062</doi></cross_references></HashMap>