Cutting edge: viral infection breaks NK cell tolerance to "missing self". Read more about Cutting edge: viral infection breaks NK cell tolerance to "missing self".
Differential regulation of chemokines by IL-17 in colonic epithelial cells. Read more about Differential regulation of chemokines by IL-17 in colonic epithelial cells.
Yersinia pestis evades TLR4-dependent induction of IL-12(p40)2 by dendritic cells and subsequent cell migration. Read more about Yersinia pestis evades TLR4-dependent induction of IL-12(p40)2 by dendritic cells and subsequent cell migration.
Normal development and activation but altered cytokine production of Fyn-deficient CD4+ T cells. Read more about Normal development and activation but altered cytokine production of Fyn-deficient CD4+ T cells.
KLRE/I1 and KLRE/I2: a novel pair of heterodimeric receptors that inversely regulate NK cell cytotoxicity. Read more about KLRE/I1 and KLRE/I2: a novel pair of heterodimeric receptors that inversely regulate NK cell cytotoxicity.
Radiation-induced CXCL16 release by breast cancer cells attracts effector T cells. Read more about Radiation-induced CXCL16 release by breast cancer cells attracts effector T cells.
Endoglycan, a member of the CD34 family of sialomucins, is a ligand for the vascular selectins. Read more about Endoglycan, a member of the CD34 family of sialomucins, is a ligand for the vascular selectins.
Apolipoprotein E-mediated immune regulation in sepsis. Read more about Apolipoprotein E-mediated immune regulation in sepsis.
Type 1 TNF receptor forms a complex with and uses Jak2 and c-Src to selectively engage signaling pathways that regulate transcription factor activity. Read more about Type 1 TNF receptor forms a complex with and uses Jak2 and c-Src to selectively engage signaling pathways that regulate transcription factor activity.
Stat6 signaling suppresses VLA-4 expression by CD8+ T cells and limits their ability to infiltrate tumor lesions in vivo. Read more about Stat6 signaling suppresses VLA-4 expression by CD8+ T cells and limits their ability to infiltrate tumor lesions in vivo.
