IL-12 as a therapeutic target for pharmacological modulation in immune-mediated and inflammatory diseases:: regulation of T helper 1/T helper 2 responses

被引:57
作者
Haskó, G [1 ]
Szabó, C [1 ]
机构
[1] Inotek Corp, Beverly, MA 01915 USA
关键词
inflammation; cytokines; autoimmune disease; interferon-gamma; interleukin-2; interleukin-10; interleukin-4; transcription factors; catecholamine; nitric oxide;
D O I
10.1038/sj.bjp.0702689
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Interleukin-12 (IL-12) is a pivotal cytokine in driving the immune system towards a T helper (Th) 1 type response and preventing a Th2 type immune profile. Therefore, IL-12 is indispensable in the defense against certain, mainly intracellular pathogens, but overproduction of this cytokine is crucially involved in the etiology of several inflammatory and autoimmune diseases. 2 Hence, IL-12 is an ideal target for pharmacological intervention in the therapy of autoimmune and inflammatory diseases. 3 The production of IL-12 and a resultant Th1 type immune response can be suppressed with several pharmacological approaches including modulation of intracellular cyclic AMP levels, glucocorticoids and nuclear factor-kappa B inhibition. IL-12 responsiveness may be inhibited using anti-IL-12 antibodies, soluble IL-12 receptors or the IL-12 p40 homodimer. 4 Exploitation of these approaches may provide novel means for the experimental therapy of a variety of pathophysiological states.
引用
收藏
页码:1295 / 1304
页数:10
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