<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(4)</volume><submitter>Ferrant J</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL) are the 2 most common B-cell lymphomas and are characterized by a dynamic crosstalk between tumor B cells and a heterogeneous, tumor-supportive microenvironment, such as immune, endothelial, and stromal components. Despite their recognized impact on the pathogenesis and prognosis of B-cell lymphoma, tumor-associated macrophages (TAM) have not been extensively explored in these diseases. In this study, we investigated mononuclear phagocyte (MNP) heterogeneity at the single-cell level and the activation profile of MNP, stromal, and endothelial compartments, in B-cell lymphoma lymph nodes compared to reactive secondary lymphoid organs. This was achieved using a combination of mass cytometry, single-cell RNA se</pubmed_abstract><journal>Blood advances</journal><pagination>1217-1232</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12917531</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Myeloid landscape profiling identifies DLBCL-specific suppressive macrophages colocalized with blood endothelial cells.</pubmed_title><pmcid>PMC12917531</pmcid><pubmed_authors>Hoareau B</pubmed_authors><pubmed_authors>Michaud HA</pubmed_authors><pubmed_authors>Launay V</pubmed_authors><pubmed_authors>Roussel M</pubmed_authors><pubmed_authors>Papa I</pubmed_authors><pubmed_authors>Pangault C</pubmed_authors><pubmed_authors>Van Acker N</pubmed_authors><pubmed_authors>Manson G</pubmed_authors><pubmed_authors>Deleurme L</pubmed_authors><pubmed_authors>Monvoisin C</pubmed_authors><pubmed_authors>Padonou F</pubmed_authors><pubmed_authors>Albaud B</pubmed_authors><pubmed_authors>Llamas Gutierrez F</pubmed_authors><pubmed_authors>Tarte K</pubmed_authors><pubmed_authors>Leonard S</pubmed_authors><pubmed_authors>Bonnefoy N</pubmed_authors><pubmed_authors>Ferrant J</pubmed_authors><pubmed_authors>Shipp MA</pubmed_authors><pubmed_authors>Pecot T</pubmed_authors><pubmed_authors>Dubec-Fleury C</pubmed_authors><pubmed_authors>Le Gallou S</pubmed_authors><pubmed_authors>Barthel A</pubmed_authors><pubmed_authors>Laurent C</pubmed_authors><pubmed_authors>Brottier C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Myeloid landscape profiling identifies DLBCL-specific suppressive macrophages colocalized with blood endothelial cells.</name><description>&lt;h4>Abstract&lt;/h4>Diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL) are the 2 most common B-cell lymphomas and are characterized by a dynamic crosstalk between tumor B cells and a heterogeneous, tumor-supportive microenvironment, such as immune, endothelial, and stromal components. Despite their recognized impact on the pathogenesis and prognosis of B-cell lymphoma, tumor-associated macrophages (TAM) have not been extensively explored in these diseases. In this study, we investigated mononuclear phagocyte (MNP) heterogeneity at the single-cell level and the activation profile of MNP, stromal, and endothelial compartments, in B-cell lymphoma lymph nodes compared to reactive secondary lymphoid organs. This was achieved using a combination of mass cytometry, single-cell RNA se</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T09:17:52.444Z</modification><creation>2026-07-09T10:47:00.089Z</creation></dates><accession>S-EPMC12917531</accession><cross_references><pubmed>41061154</pubmed><doi>10.1182/bloodadvances.2024015689</doi></cross_references></HashMap>