<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE337nnn/GSE337601/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE337601</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>XCR1+ and CD11b+ migratory dendritic cells cooperate for the crosspriming of intratumoral CD8+ T cells with a tissue-resident memory phenotype [RNA-Seq]</name><description>The composition and diversity of tumor-infiltrating CD8+ T cell populations have important consequences on the development of anti-tumor immunity. In a murine model of lung cancer, we have addressed the role of dendritic cell subsets on the generation of various types of tumor-infiltrating CD8+ T cells. We show that CD44+PD1- effector and PD1+TIM3+ exhausted, tumor-infiltrating CD8+ T cells require XCR1+ DC1s but not IRF4-dependent CD11b+ DC2s. By contrast, CD103+CD69+ TRM-like, tumor-infiltrating CD8+ T cells require both DC1s and DC2s. The same requirement is found in tumor-draining lymph nodes where we identify CD103+ TRM-like precursors that are dependent on both XCR1+ DC1s and CD11b+, migratory DC2s. Mechanistically, we evidence that both types of migratory DCs cooperate. Mild TCR triggering by low MHCI-peptide density at the surface of cross-presenting migratory DC2s and low IL-12 support TGFb-dependent TRM specification in lymph nodes. High TCR triggering and high MHCI-peptide density at the surface of cross-presenting migratory DC1s and high IL-12 support proliferative expansion and CXCR6 acquisition. Altogether, these findings highlight the induction of intratumoral TRM-like cells under the collective aegis of multiple DCs subsets within tumor-draining lymph nodes reconciliating TRM phenotype instruction with proliferative expansion.</description><dates><publication>2026/07/07</publication></dates><accession>GSE337601</accession><cross_references><GSM>GSM9858560</GSM><GSM>GSM9858561</GSM><GSM>GSM9858562</GSM><GSM>GSM9858540</GSM><GSM>GSM9858563</GSM><GSM>GSM9858541</GSM><GSM>GSM9858542</GSM><GSM>GSM9858564</GSM><GSM>GSM9858565</GSM><GSM>GSM9858543</GSM><GSM>GSM9858566</GSM><GSM>GSM9858544</GSM><GSM>GSM9858567</GSM><GSM>GSM9858545</GSM><GSM>GSM9858568</GSM><GSM>GSM9858546</GSM><GSM>GSM9858547</GSM><GSM>GSM9858569</GSM><GSM>GSM9858548</GSM><GSM>GSM9858549</GSM><GSM>GSM9858570</GSM><GSM>GSM9858550</GSM><GSM>GSM9858551</GSM><GSM>GSM9858552</GSM><GSM>GSM9858553</GSM><GSM>GSM9858554</GSM><GSM>GSM9858555</GSM><GSM>GSM9858556</GSM><GSM>GSM9858557</GSM><GSM>GSM9858535</GSM><GSM>GSM9858536</GSM><GSM>GSM9858558</GSM><GSM>GSM9858559</GSM><GSM>GSM9858537</GSM><GSM>GSM9858538</GSM><GSM>GSM9858539</GSM><GPL>34328</GPL><GSE>337601</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>