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Transcriptional profiling of tumor microenvironment in B2M KO CD40-treated B16 tumors implanted in mice

GSE240148 Mus musculus Expression profiling by high throughput sequencing 16 samples 2026/02/02 GPL19057
Summary
The immune changes induced by loss of antigen presentation by tumor cells, a common mechanism of acquired resistance to immunotherapy, as well as the mechanisms by which CD40 agonist treatment controls the growth of B2m-null tumors, are unknown. We performed single-cell RNA-seq of total tumor-infiltrating immune cells in control and B2m-null tumors treated with isotype control or CD40 agonist antibodies to identify changes in immune cell states due to tumor cell loss of B2m and agonist CD40 treatment.
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NCBI GEO page ↗ Paper (PMID 41676732) ↗ {# Names what the click gives you. "Open in finder" meant nothing to a visitor who arrived from a search engine and has never seen the tool. #} Find more mouse RNA-seq datasets →
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