We have a suspicion that you are an automated web bot software, not a real user. To keep our site fast for other users, we have slowed down this page. The slowdown will gradually disappear. If you think this is a mistake, please contact us at genome-www@soe.ucsc.edu. Also note that all data for hgGeneGraph can be obtained through our public MySQL server and all our software source code is available and can be installed locally onto your own computer. If you are unsure how to use these resources, do not hesitate to contact us.
UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

◀ Back to IL15

IL12A — IL15

Text-mined interactions from Literome

Milano et al., Clin Exp Immunol 2002 (Leishmaniasis, Visceral) : Since IL-15 , in the presence of anti-IL-4 MoAb, caused a further increase in IL-12 production and led to a significant production of IFN-gamma, one of its indirect effects on Th1 cell activation could be due to the latter 's effect on Th2 cytokines such as IL-4
Derre et al., J Immunol 2002 (Melanoma) : We show that IL-12 induces the expression of NKG2-A and/or CD94 by CD8 ( + ) T cells in culture, and that this induction was mediated neither by IFN-gamma nor by IL-15
Strengell et al., J Immunol 2003 : We have previously shown that IL-15 and IL-21 induce the expression of IFN-gamma, T-bet, IL-12R beta 2, and IL-18R genes both in NK and T cells
Croy et al., J Reprod Immunol 2003 : Here, we review recent studies showing that IL-15 is the critical cytokine controlling uNK cell differentiation and that uNK cells are activated by either IL-12 or IL-18 and by other factors when both IL-12 and IL-18 are genetically absent from implantation sites
Musikacharoen et al., Blood 2005 : Interleukin-15 induces IL-12 receptor beta1 gene expression through PU.1 and IRF 3 by targeting chromatin remodeling
Watkins et al., J Immunol 2007 (Carcinoma, Lewis Lung...) : Analysis of tumor infiltrating macrophages and distal TAMs revealed that IL-12 , both in vivo and in vitro, induced a rapid ( < 90 min ) reduction of tumor supportive macrophage activities ( IL-10, MCP-1, migration inhibitory factor, and TGFbeta production ) and a concomitant increase in proinflammatory and proimmunogenic activities ( TNF-alpha, IL-15 , and IL-18 production )
Haeberlein et al., Eur J Immunol 2010 (Leishmaniasis, Visceral) : Here, we investigated whether IL-15 or IL-18 mediate the activity of IL-12 or function as independent activators of NK cells
Marshall et al., J Immunol 2010 (Arenaviridae Infections) : IL-12 , IL-15, IL-18, and IFN-gamma were not individually required for sensitization to produce IFN-gamma, but IL-15 was required for upregulation of granzyme B
Ferret-Bernard et al., Vet Res 2011 : The IL-15 increases IL-12 production by an amplifying feedback loop involving CD40
Kishida et al., Clin Dev Immunol 2012 (Hepatitis C, Chronic) : IL-15 was increased at the end of induction therapy in both early virologic responders ( EAVRs ) and late virologic responders ( LAVRs ) ; CXCL-8, CXCL-10, and CCL-4 levels were significantly decreased ( P < 0.05 ) in EAVR but not in LAVR during NCT, and IL-12 increased significantly ( P < 0.05 ) and CXCL-8 decreased significantly ( P < 0.05 ) after the end of NCT in EAVR but not in LAVR
Hegde et al., Cell Immunol 1995 (Neoplasms, Experimental) : AK-5 tumor induced expression of interleukin-12 : role of IL-12 in NK-mediated AK-5 regression
Wu et al., Eur J Immunol 1997 : Among 16 cytokines tested, IL-2, IL-7 and IL-15 markedly induced IL-12Rbeta1 expression and IL-12 binding on resting PBMC, whereas IL-1alpha and tumor necrosis factor-alpha had a minimal enhancing effect
Avice et al., J Immunol 1998 : IL-15 promotes IL-12 production by human monocytes via T cell dependent contact and may contribute to IL-12 mediated IFN-gamma secretion by CD4+ T cells in the absence of TCR ligation