<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>116(24)</volume><submitter>Pizzolato G</submitter><pubmed_abstract>γδ T lymphocytes represent ∼1% of human peripheral blood mononuclear cells and even more cells in most tissues of vertebrates. Although they have important anticancer functions, most current single-cell RNA sequencing (scRNA-seq) studies do not identify γδ T lymphocytes because their transcriptomes at the single-cell level are unknown. Here we show that high-resolution clustering of large scRNA-seq datasets and a combination of gene signatures allow the specific detection of human γδ T lymphocytes and identification of their T cell receptor (TCR)Vδ1 and TCRVδ2 subsets in large datasets from complex cell mixtures. In &lt;i>t&lt;/i>-distributed stochastic neighbor embedding plots from blood and tumor samples, the few γδ T lymphocytes appear collectively embedded between cytotoxic CD8 T and NK cell</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>11906-11915</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6576116</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-cell RNA sequencing unveils the shared and the distinct cytotoxic hallmarks of human TCRVδ1 and TCRVδ2 γδ T lymphocytes.</pubmed_title><pmcid>PMC6576116</pmcid><pubmed_authors>Meraviglia S</pubmed_authors><pubmed_authors>Fournie JJ</pubmed_authors><pubmed_authors>Kaminski H</pubmed_authors><pubmed_authors>Labourdette D</pubmed_authors><pubmed_authors>Quillet-Mary A</pubmed_authors><pubmed_authors>Pizzolato G</pubmed_authors><pubmed_authors>Cadot S</pubmed_authors><pubmed_authors>Ysebaert L</pubmed_authors><pubmed_authors>Martins F</pubmed_authors><pubmed_authors>Merville P</pubmed_authors><pubmed_authors>Dechanet-Merville J</pubmed_authors><pubmed_authors>Franchini DM</pubmed_authors><pubmed_authors>Dieli F</pubmed_authors><pubmed_authors>Pont F</pubmed_authors><pubmed_authors>Tosolini M</pubmed_authors><pubmed_authors>Poupot M</pubmed_authors><pubmed_authors>Laurent C</pubmed_authors><pubmed_authors>Valle C</pubmed_authors><pubmed_authors>Milpied P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell RNA sequencing unveils the shared and the distinct cytotoxic hallmarks of human TCRVδ1 and TCRVδ2 γδ T lymphocytes.</name><description>γδ T lymphocytes represent ∼1% of human peripheral blood mononuclear cells and even more cells in most tissues of vertebrates. Although they have important anticancer functions, most current single-cell RNA sequencing (scRNA-seq) studies do not identify γδ T lymphocytes because their transcriptomes at the single-cell level are unknown. Here we show that high-resolution clustering of large scRNA-seq datasets and a combination of gene signatures allow the specific detection of human γδ T lymphocytes and identification of their T cell receptor (TCR)Vδ1 and TCRVδ2 subsets in large datasets from complex cell mixtures. In &lt;i>t&lt;/i>-distributed stochastic neighbor embedding plots from blood and tumor samples, the few γδ T lymphocytes appear collectively embedded between cytotoxic CD8 T and NK cell</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-04-29T13:02:10.965Z</modification><creation>2020-05-21T19:56:30Z</creation></dates><accession>S-EPMC6576116</accession><cross_references><pubmed>31118283</pubmed><doi>10.1073/pnas.1818488116</doi></cross_references></HashMap>