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Here we compared the gene expression profiles of T cells in pulmonary granulomas, bronchoalveolar lavage and blood of Mtb-infected rhesus macaques to identify granuloma-enriched T cell genes. TNFRSF8/CD30 was among the top genes that was upregulated in both CD4 and CD8 granuloma T cells and independent of bacterial loads. Transcriptomic profiling of lung T cells from Mtb-infected mixed bone marrow chimeric mice showed that CD30 directly promotes CD4 T cell differentiation and effector molecule expression. Moreover, in mice CD30 expression on CD4 T cells is required for survival of Mtb infection. These results show the CD30 co-stimulatory axis is highly upregulated on granuloma T cells and is critical for the generation of protective T cell responses against Mtb infection. Overall design: RNA-seq of mouse CD4 T-cells. Balanced 2-factor design (WT/KO MTb Activated/ Naïve), N=4 mice per group</long_description><tag>xref:PubMed:37097292</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Gene expression profiling of granuloma T cells in M. tuberculosis infected rhesus macaques reveals a critical role for CD30 [Mus musculus]</name><description>Gene expression profiling of granuloma T cells in M. tuberculosis infected rhesus macaques reveals a critical role for CD30 [Mus musculus]</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-03-31</first_public></dates><accession>PRJNA948056</accession><cross_references><GEO>GSE228113</GEO><taxon>10090</taxon><PubMed>37097292</PubMed></cross_references></HashMap>