<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>120(1)</volume><submitter>Derre L</submitter><pubmed_abstract>The function of antigen-specific CD8+ T cells, which may protect against both infectious and malignant diseases, can be impaired by ligation of their inhibitory receptors, which include CTL-associated protein 4 (CTLA-4) and programmed cell death 1 (PD-1). Recently, B and T lymphocyte attenuator (BTLA) was identified as a novel inhibitory receptor with structural and functional similarities to CTLA-4 and PD-1. BTLA triggering leads to decreased antimicrobial and autoimmune T cell responses in mice, but its functions in humans are largely unknown. Here we have demonstrated that as human viral antigen-specific CD8+ T cells differentiated from naive to effector cells, their surface expression of BTLA was gradually downregulated. In marked contrast, human melanoma tumor antigen-specific effecto</pubmed_abstract><journal>The Journal of clinical investigation</journal><pagination>157-67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2799219</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>BTLA mediates inhibition of human tumor-specific CD8+ T cells that can be partially reversed by vaccination.</pubmed_title><pmcid>PMC2799219</pmcid><pubmed_authors>Speiser DE</pubmed_authors><pubmed_authors>Rimoldi D</pubmed_authors><pubmed_authors>Pastor S</pubmed_authors><pubmed_authors>Michielin O</pubmed_authors><pubmed_authors>Olive D</pubmed_authors><pubmed_authors>Romero P</pubmed_authors><pubmed_authors>Derre L</pubmed_authors><pubmed_authors>Rivals JP</pubmed_authors><pubmed_authors>Jandus C</pubmed_authors></additional><is_claimable>false</is_claimable><name>BTLA mediates inhibition of human tumor-specific CD8+ T cells that can be partially reversed by vaccination.</name><description>The function of antigen-specific CD8+ T cells, which may protect against both infectious and malignant diseases, can be impaired by ligation of their inhibitory receptors, which include CTL-associated protein 4 (CTLA-4) and programmed cell death 1 (PD-1). Recently, B and T lymphocyte attenuator (BTLA) was identified as a novel inhibitory receptor with structural and functional similarities to CTLA-4 and PD-1. BTLA triggering leads to decreased antimicrobial and autoimmune T cell responses in mice, but its functions in humans are largely unknown. Here we have demonstrated that as human viral antigen-specific CD8+ T cells differentiated from naive to effector cells, their surface expression of BTLA was gradually downregulated. In marked contrast, human melanoma tumor antigen-specific effecto</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jan</publication><modification>2025-05-18T11:22:09.647Z</modification><creation>2025-05-18T11:22:09.647Z</creation></dates><accession>S-EPMC2799219</accession><cross_references><pubmed>20038811</pubmed><doi>10.1172/JCI40070</doi><doi>10.1172/jci40070</doi></cross_references></HashMap>