Forrester M A, Robertson L, Bayoumi N, Keavney B D, Barker R N, Vickers M A
Immunity, Infection and Inflammation, Institute of Medical Sciences, University of Aberdeen, Aberdeen, UK.
Clin Exp Immunol. 2014 Nov;178(2):373-83. doi: 10.1111/cei.12408.
Although it is widely believed that interleukin (IL)-27 is anti-inflammatory, its role in controlling human immune responses is not fully established. In particular, its interactions with T helper type 17 (Th)17 cytokines are unclear. Our aims were to establish the relationships between IL-27 and proinflammatory cytokines, including IL-17A, in human sera and cultures of peripheral blood mononuclear cells. Plasma IL-27 levels in 879 healthy humans from 163 families varied widely, but with relatively low heritability (19%). Despite IL-27 including a subunit encoded by Epstein-Barr virus-induced gene 3 (EBI3), there was no correlation of levels with serological evidence of infection with the virus. Although IL-27 has been reported to inhibit IL-17A production, we demonstrated a strong positive correlation in sera, but lower correlations of IL-27 with other proinflammatory cytokines. We verified that IL-27 inhibited IL-17A production by human peripheral blood T cells in vitro, but not that it stimulated IL-10 secretion. Importantly, addition of IL-17A decreased IL-27 production by stimulated T cells but had the opposite effect on resting T cells. Together, these data suggest a model whereby IL-27 and IL-17A exerts complex reciprocal effects to boost inflammatory responses, but restrain resting cells to prevent inappropriate activation.
尽管人们普遍认为白细胞介素(IL)-27具有抗炎作用,但其在控制人类免疫反应中的作用尚未完全明确。特别是,它与17型辅助性T细胞(Th)17细胞因子的相互作用尚不清楚。我们的目的是确定IL-27与促炎细胞因子(包括IL-17A)在人血清和外周血单核细胞培养物中的关系。来自163个家庭的879名健康人的血浆IL-27水平差异很大,但遗传度相对较低(19%)。尽管IL-27包含一个由爱泼斯坦-巴尔病毒诱导基因3(EBI3)编码的亚基,但血浆IL-27水平与该病毒感染的血清学证据并无相关性。虽然有报道称IL-27可抑制IL-17A的产生,但我们发现血清中IL-27与IL-17A呈强正相关,而IL-27与其他促炎细胞因子的相关性较低。我们证实,IL-27在体外可抑制人外周血T细胞产生IL-17A,但不能刺激IL-10的分泌。重要的是,添加IL-17A可降低受刺激T细胞产生IL-27,但对静息T细胞则有相反的作用。总之,这些数据提示了一种模型,即IL-27和IL-17A通过复杂的相互作用来增强炎症反应,但抑制静息细胞以防止不适当的激活。