Cutting edge: Identification of c-Rel-dependent and -independent pathways of IL-12 production during infectious and inflammatory stimuli

被引:88
作者
Mason, N
Aliberti, J
Caamano, JC
Liou, HC
Hunter, CA
机构
[1] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
[2] NIAID, Parasit Dis Lab, Immunobiol Sect, NIH, Bethesda, MD 20892 USA
[3] Univ Birmingham, Sch Med, MRC, Ctr Immune Regulat, Birmingham, W Midlands, England
[4] Cornell Univ, Coll Med, Cornell Div Immunol, Dept Med, New York, NY 10021 USA
关键词
D O I
10.4049/jimmunol.168.6.2590
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The production of IL-12 is required for immunity to many intracellular pathogens. Recent studies have shown that c-Rel, a member of the NF-kB family of transcription factors, is essential for LPS-induced IL-12p40 production by macrophages. In this study, we demonstrate that c-Rel is also required for IL-12p40 production by macrophages in response to Cotyne-bacterium parvum, CpG oligodeoxynucleotides, anti-CD40 and low molecular weight hyaluronic acid. However, c-Rel(-/-) mice infected with Toxoplasma gondii produce comparable amounts of IL-12p40 to infected wild-type mice and have an IL-12-dependent mechanism of resistance to this infection. Furthermore, c-Rel was not required for IL-12p40 production by macrophages or dendritic cells in response to soluble Toxoplasma Ag, and neutrophils from c-Rel(-/-) mice contain normal amounts of preformed IL-12p40. Together these studies reveal the presence of c-Rel-dependent pathways critical for IL12p40 production in response to inflammatory stimuli and demonstrate a novel c-Rel-independent pathway of IL-12p40 production during toxoplasmosis.
引用
收藏
页码:2590 / 2594
页数:5
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