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. 2018 Apr 1;31(3):206–222. doi: 10.1089/vim.2017.0051

Table 4.

Inflammatory Gene Expression in SHIVnef Compared to SIV-Infected Rhesus Macaques

Gene Gene symbol Fold change in SHIVnef infection Cellular function/pathway
Interleukin 12 receptor beta 1 subunit IL-12RB1 −6.7 JAK-STAT signaling pathway
CD40 ligand CD40L −6.4 Immunoglobulin class switch, adaptive immunity
TNF (ligand) superfamily, member 14 TNFSD14 −5.7 NF-kB signaling pathway
Lymphotoxin alpha LTA −4.8 Inflammatory, immunostimulatory, and antiviral responses, apoptosis
Chemokine (C-C) ligand 17 CCL17 −4.5 Antimicrobial, trafficking, and activation of mature T cells
Interleukin 3 IL-3 −4.3 Cell growth, differentiation, and apoptosis
Interleukin 1 receptor type 1 IL1R1 −4.1 Interleukin 1 receptor antagonist, MAPK signaling pathway
Fractalkine CX3CL1 −4.0 T lymphocyte and monocyte chemoattractor
Interleukin 13 receptor subunit alpha-2-like LOC708339 (Mmu) −3.4 JAK-STAT signaling pathway
Interleukin 13 IL-13 −3.3 B cell maturation and differentiation
Osteoprotegerin TNFRSF11B −3.0 Blocks the binding of TNF-related apoptosis-inducing ligand (TRAIL)
CD70 CD70 −3.0 TNF ligand family, regulates B cell activation
Fas ligand FasL −2.8 TNF superfamily, apoptosis
Interleukin 6 IL-6 2.8 Multifunctional cytokine, inflammatory response
Chemokine (C-C) receptor 8 CCR8 2.9 G-protein-coupled receptor signaling pathway
Interferon-inducible T cell alpha chemoattractant CXCL11 3.0 Chemotactic for activated T cells, CXCR3 signaling pathway
TNF (ligand) superfamily, member 13b TNFSF13B 3.0 NF-kB signaling pathway
Monocyte chemotactic protein 1 CCL2 3.7 Recruits monocytes, memory T cells, and dendritic cells to the sites of inflammation
Macrophage inflammatory protein 3a CCL20 3.8 Strongly chemotactic for lymphocytes
Monocyte chemotactic protein 3-like LOC714751 (Mmu) 4.1 Attracts macrophages during inflammation
Interleukin 1 receptor, type 2 IL-1R2 5.0 MAPK signaling pathway
Macrophage inflammatory protein 3 CCL23 11.6 Highly chemotactic for resting T cells and monocytes

Lung RNA samples were amplified using the PCR targeted array for Rhesus Macaque Inflammatory Cytokines & Receptors (SABiosciences) in a BioRad iCycler iQ, as per manufacturer protocols. The housekeeping genes beta-2-microglobulin and hypoxanthine-guanine phosphoribosyltransferase-like were used for normalization. Gene expression was determined via the ΔΔCt method; fold changes were calculated based on difference in gene expression between six SHIVnef- and two SIVmac239-infected macaques. Statistical analyses were not performed given the small sample size in the SIV group. Only the genes with altered expression of genes at fold change cutoff of ±2.7 are shown. Mmu, Macaca mulatta.