Colpaert Stefaan, Vanstraelen Kathleen, Liu Zhanju, Penninckx Freddy, Geboes Karel, Rutgeerts Paul, Ceuppens Jan
Laboratory of Experimental Immunology, University Hospital and Katholieke Universiteit Leuven, Leuven, Belgium.
Clin Immunol. 2002 Jan;102(1):68-76. doi: 10.1006/clim.2001.5149.
We investigated whether a lack of IL-10 production or responsiveness could be involved in Crohn's disease pathogenesis. Lamina propria mononuclear cells, isolated from the ilea of Crohn's disease patients (n = 16) and controls (n = 13), were activated with anti-CD3 mAb in the presence of CD80 transfectants or LPS +/- IFN-gamma. No evidence for deficient IL-10 production by either T cells or macrophages in Crohn's disease was found. However, the efficacy of rhIL-10 to down-regulate IFN-gamma and especially TNF production in cell cultures from the involved tissues of Crohn's disease patients was poor, and the use of an anti-IL-10R mAb even provided evidence for proinflammatory effects of IL-10. This lack of IL-10 effect possibly results from IL-12 activity. We conclude that IL-10 exhibits poor anti- and even potential proinflammatory effects on ileal Crohn's disease lamina propria. These data might explain the lack of therapeutic efficacy when IL-10 is given to Crohn's disease patients.
我们研究了白细胞介素-10(IL-10)分泌缺乏或反应性缺失是否与克罗恩病的发病机制有关。从克罗恩病患者(n = 16)和对照组(n = 13)的回肠中分离出固有层单核细胞,在存在CD80转染子或脂多糖(LPS)+/-γ干扰素(IFN-γ)的情况下,用抗CD3单克隆抗体(mAb)进行激活。未发现克罗恩病中T细胞或巨噬细胞分泌IL-10存在缺陷的证据。然而,重组人IL-10(rhIL-10)下调克罗恩病患者受累组织细胞培养物中IFN-γ尤其是肿瘤坏死因子(TNF)产生的效果较差,并且使用抗IL-10受体mAb甚至提供了IL-10具有促炎作用的证据。这种IL-10效应的缺乏可能是由IL-12活性导致的。我们得出结论,IL-10对回肠克罗恩病固有层表现出较差的抗炎作用,甚至具有潜在的促炎作用。这些数据可能解释了给克罗恩病患者使用IL-10时治疗效果不佳的原因。