<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(12)</volume><submitter>Zhu W</submitter><pubmed_abstract>T and B cell receptor (TCR and BCR, respectively) Vβ or immunoglobulin heavy chain complementarity-determining region 3 sequencing allows monitoring of repertoire changes through recognition, clonal expansion, affinity maturation, and T or B cell activation in response to antigen. TCR and BCR repertoire analysis can advance understanding of antitumor immune responses in the tumor microenvironment. TCR and BCR repertoires of sorted CD4&lt;sup>+&lt;/sup>, CD8&lt;sup>+&lt;/sup> or CD19&lt;sup>+&lt;/sup> cells in tumor, non-tumoral distant tissue (NT), and peripheral compartments (blood/draining lymph node [P]) from 47 non-small cell lung cancer (NSCLC) patients (age&lt;sub>median&lt;/sub> = 68 y) were sequenced. The clonotype spectra were assessed among different tissues and correlated with clinical and immunologica</pubmed_abstract><journal>Oncoimmunology</journal><pagination>e1051922</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4635865</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A high density of tertiary lymphoid structure B cells in lung tumors is associated with increased CD4&lt;sup>+&lt;/sup> T cell receptor repertoire clonality.</pubmed_title><pmcid>PMC4635865</pmcid><pubmed_authors>Hammond SA</pubmed_authors><pubmed_authors>Damotte D</pubmed_authors><pubmed_authors>Sebastian Y</pubmed_authors><pubmed_authors>Higgs BW</pubmed_authors><pubmed_authors>Valge-Archer V</pubmed_authors><pubmed_authors>Germain C</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Yao Y</pubmed_authors><pubmed_authors>Devi P</pubmed_authors><pubmed_authors>Lehmann K</pubmed_authors><pubmed_authors>Dieu-Nosjean MC</pubmed_authors><pubmed_authors>Knockaert S</pubmed_authors><pubmed_authors>Validire P</pubmed_authors><pubmed_authors>Zhu W</pubmed_authors><pubmed_authors>Brohawn P</pubmed_authors></additional><is_claimable>false</is_claimable><name>A high density of tertiary lymphoid structure B cells in lung tumors is associated with increased CD4&lt;sup>+&lt;/sup> T cell receptor repertoire clonality.</name><description>T and B cell receptor (TCR and BCR, respectively) Vβ or immunoglobulin heavy chain complementarity-determining region 3 sequencing allows monitoring of repertoire changes through recognition, clonal expansion, affinity maturation, and T or B cell activation in response to antigen. TCR and BCR repertoire analysis can advance understanding of antitumor immune responses in the tumor microenvironment. TCR and BCR repertoires of sorted CD4&lt;sup>+&lt;/sup>, CD8&lt;sup>+&lt;/sup> or CD19&lt;sup>+&lt;/sup> cells in tumor, non-tumoral distant tissue (NT), and peripheral compartments (blood/draining lymph node [P]) from 47 non-small cell lung cancer (NSCLC) patients (age&lt;sub>median&lt;/sub> = 68 y) were sequenced. The clonotype spectra were assessed among different tissues and correlated with clinical and immunologica</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2025-04-19T06:26:12.166Z</modification><creation>2019-03-27T02:01:29Z</creation></dates><accession>S-EPMC4635865</accession><cross_references><pubmed>26587322</pubmed><doi>10.1080/2162402X.2015.1051922</doi></cross_references></HashMap>