<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(9)</volume><submitter>Srinivas N</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The presence of tertiary lymphoid structures (TLS) in solid tumors, including Merkel cell carcinoma (MCC), is associated with a better prognosis and a better response to immunotherapy with immune checkpoint inhibition (ICI). The detailed mechanisms by which TLS influence antitumor immune responses are only partially understood.&lt;h4>Methods&lt;/h4>Clinically annotated tumor tissues of 27 patients with MCC were obtained prior to ICI therapy. Tumor samples were subjected to transcriptomic and multiplex immuno-visual profiling, T-cell receptor (TCR) clonotype mapping, as well as-in selected cases-spatial transcriptomics to comprehensively characterize the tumor immune microenvironment.&lt;h4>Results&lt;/h4>Weighted gene co-expression network analysis (WGCNA) of transcriptomic data in </pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pagination>e012224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12458699</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tertiary lymphoid structures in Merkel cell carcinoma facilitate naive and central memory T-cell infiltration linked to immunotherapy response.</pubmed_title><pmcid>PMC12458699</pmcid><pubmed_authors>Pino MJ</pubmed_authors><pubmed_authors>Lei KC</pubmed_authors><pubmed_authors>Stoffels I</pubmed_authors><pubmed_authors>Gao J</pubmed_authors><pubmed_authors>Lui WO</pubmed_authors><pubmed_authors>Dalkoohi M</pubmed_authors><pubmed_authors>Leiter U</pubmed_authors><pubmed_authors>Ugurel S</pubmed_authors><pubmed_authors>Gambichler T</pubmed_authors><pubmed_authors>Mohr P</pubmed_authors><pubmed_authors>Spassova I</pubmed_authors><pubmed_authors>Cheung PF</pubmed_authors><pubmed_authors>Srinivas N</pubmed_authors><pubmed_authors>Livingstone E</pubmed_authors><pubmed_authors>Giglio G</pubmed_authors><pubmed_authors>Engblom C</pubmed_authors><pubmed_authors>Kitanovski S</pubmed_authors><pubmed_authors>Becker JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tertiary lymphoid structures in Merkel cell carcinoma facilitate naive and central memory T-cell infiltration linked to immunotherapy response.</name><description>&lt;h4>Background&lt;/h4>The presence of tertiary lymphoid structures (TLS) in solid tumors, including Merkel cell carcinoma (MCC), is associated with a better prognosis and a better response to immunotherapy with immune checkpoint inhibition (ICI). The detailed mechanisms by which TLS influence antitumor immune responses are only partially understood.&lt;h4>Methods&lt;/h4>Clinically annotated tumor tissues of 27 patients with MCC were obtained prior to ICI therapy. Tumor samples were subjected to transcriptomic and multiplex immuno-visual profiling, T-cell receptor (TCR) clonotype mapping, as well as-in selected cases-spatial transcriptomics to comprehensively characterize the tumor immune microenvironment.&lt;h4>Results&lt;/h4>Weighted gene co-expression network analysis (WGCNA) of transcriptomic data in </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T19:36:38.738Z</modification><creation>2026-04-30T03:12:24.845Z</creation></dates><accession>S-EPMC12458699</accession><cross_references><pubmed>40992783</pubmed><doi>10.1136/jitc-2025-012224</doi></cross_references></HashMap>