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        <identifier>oai:figshare.com:article/34038837</identifier>
        <datestamp>2026-10-01T04:42:35Z</datestamp>
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          <dc:title>Table 2_Transcriptomic evidence of an IFN-gamma-associated inflammatory state in active visceral leishmaniasis: an exploratory comparison with pediatric HLH.xlsx</dc:title>
          <dc:creator>Taoli Suo (25151829)</dc:creator>
          <dc:creator>Jing Zhang (23775)</dc:creator>
          <dc:creator>Yanli Chen (1410277)</dc:creator>
          <dc:creator>Hongyu Shi (3611147)</dc:creator>
          <dc:creator>Haiyan Lu (835712)</dc:creator>
          <dc:subject>Clinical Microbiology</dc:subject>
          <dc:subject>CXCL10</dc:subject>
          <dc:subject>CXCL9</dc:subject>
          <dc:subject>hemophagocytic lymphohistiocytosis</dc:subject>
          <dc:subject>IFN-gamma</dc:subject>
          <dc:subject>single-cell transcriptome</dc:subject>
          <dc:subject>STAT1</dc:subject>
          <dc:subject>visceral leishmaniasis</dc:subject>
          <dc:description>Background&lt;p&gt;Visceral leishmaniasis (VL) can progress to secondary hemophagocytic lymphohistiocytosis (HLH), but transcriptomic similarities between active VL and pediatric HLH remain uncertain.&lt;/p&gt;Methods&lt;p&gt;We integrated VL whole-blood expression data (GSE125992), sorted CD68-positive monocyte bulk-expression data from pediatric HLH and severe sepsis (GSE150707), and supportive Leishmania-infected mouse spleen single-cell data (GSE240385). Differential expression, pathway enrichment, an exploratory 132-gene HLH-versus-sepsis-derived ssGSEA score, FARDEEP-LM22 deconvolution, signature-excluded WGCNA, CellChat, and a refitted three-gene classifier were evaluated.&lt;/p&gt;Results&lt;p&gt;Active VL showed IFN-gamma-associated expression changes, including higher CXCL9 and CXCL10. The exploratory 132-gene score was higher in ActiveCase than EHC samples (Mann-Whitney P = 0.000637). Across 22 deconvolved cell types, only M1 macrophages showed an FDR-supported positive correlation with this score (rho = 0.787, BH q = 0.000503). After all 132 score genes were excluded before network construction, a 124-gene magenta module remained associated with the score (rho = 0.837, BH q = 4.29 × 10^-5). A refitted IFNG/GBP5/MX2 classifier achieved a same-study validation AUC of 0.917 (bootstrap 95% CI 0.733-1.000), but the validation set contained only 16 samples.&lt;/p&gt;Conclusion&lt;p&gt;These public datasets support an IFN-gamma-associated inflammatory state in active VL and exploratory cross-compartment convergence with pediatric HLH. The 132-gene score, deconvolution, network, and classifier results are hypothesis-generating and do not establish HLH specificity, cellular causality, independent external validity, or clinical HLH prediction.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T04:42:35Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fcimb.2026.1924856</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_2_Transcriptomic_evidence_of_an_IFN-gamma-associated_inflammatory_state_in_active_visceral_leishmaniasis_an_exploratory_comparison_with_pediatric_HLH_xlsx/34038837</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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