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. Author manuscript; available in PMC: 2020 Feb 15.
Published in final edited form as: J Immunol. 2019 Jan 11;202(4):1112–1123. doi: 10.4049/jimmunol.1801270

Table 2. In the absence of Ikaros, resting CD4 T cells up-regulate expression of pathways linked to the response to type I Interferons.

Results of GSEA analyses of microarray data for freshly isolated Ikflox x dLck-Cre [Cre+] and Ikflox (no Cre) [Cre] CD4 T cells. In total, 152 gene sets were significantly enriched in Cre+ relative to Cre- CD4 T cells (FDR q<0.25). Examples of enhanced biological processes, functions and pathways are shown. ES: Enrichment score; NES: Normalized enrichment score.

Gene Set Name Gene Set
Size
ES NES Nominal
p value
FDR
q value
Hallmark Interferon Alpha Response 87 0.63 2.23 <0.001 0.0033
Reactome Interferon Alpha Beta Signaling 39 0.73 2.25 <0.001 0.0055
GO Response to Type I Interferon 41 0.67 2.14 <0.001 0.0244
Reactome Interferon Signaling 115 0.55 2.06 <0.001 0.0349
GO Response to Interferon Alpha 16 0.78 2.04 <0.001 0.0358
Reactome RIG MDA5 Mediated Induction of IFN Alpha Beta Pathway 53 0.59 1.99 <0.001 0.0541
GO Response to Interferon Beta 20 0.72 1.94 <0.001 0.0756