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TL1A synergizes with IL-12 and IL-18 to enhance IFN-gamma production in human T cells and NK cells.
Papadakis, Konstantinos A; Prehn, John L; Landers, Carol; Han, Qiwei; Luo, Xia; Cha, Stephanie C; Wei, Ping; Targan, Stephan R.
Affiliation
  • Papadakis KA; Cedars-Sinai Inflammatory Bowel Disease Center, Los Angeles, CA 90048, USA.
J Immunol ; 172(11): 7002-7, 2004 Jun 01.
Article in En | MEDLINE | ID: mdl-15153521
ABSTRACT
TL1A, a recently described TNF-like cytokine that interacts with DR3, costimulates T cells and augments anti-CD3 plus anti-CD28 IFN-gamma production. In the current study we show that TL1A or an agonistic anti-DR3 mAb synergize with IL-12/IL-18 to augment IFN-gamma production in human peripheral blood T cells and NK cells. TL1A also enhanced IFN-gamma production by IL-12/IL-18 stimulated CD56(+) T cells. When expressed as fold change, the synergistic effect of TL1A on cytokine-induced IFN-gamma production was more pronounced on CD4(+) and CD8(+) T cells than on CD56(+) T cells or NK cells. Intracellular cytokine staining showed that TL1A significantly enhanced both the percentage and the mean fluorescence intensity of IFN-gamma-producing T cells in response to IL-12/IL-18. The combination of IL-12 and IL-18 markedly up-regulated DR3 expression in NK cells, whereas it had minimal effect in T cells. Our data suggest that TL1A/DR3 pathway plays an important role in the augmentation of cytokine-induced IFN-gamma production in T cells and that DR3 expression is differentially regulated by IL-12/IL-18 in T cells and NK cells.
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Collection: 01-internacional Database: MEDLINE Main subject: Killer Cells, Natural / T-Lymphocytes / Interferon-gamma / Tumor Necrosis Factor-alpha / Interleukin-12 / Interleukin-18 Limits: Humans Language: En Journal: J Immunol Year: 2004 Type: Article Affiliation country: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Killer Cells, Natural / T-Lymphocytes / Interferon-gamma / Tumor Necrosis Factor-alpha / Interleukin-12 / Interleukin-18 Limits: Humans Language: En Journal: J Immunol Year: 2004 Type: Article Affiliation country: United States