Smith Andrew M, Sewell Gavin W, Levine Adam P, Chew Thean S, Dunne Jenny, O'Shea Nuala R, Smith Philip J, Harrison Penelope J, Macdonald Carol M, Bloom Stuart L, Segal Anthony W
Microbial Diseases, Eastman Dental Institute, University College London, London, UK.
Immunology. 2015 Jan;144(1):45-55. doi: 10.1111/imm.12338.
Crohn's disease (CD) is a complex and highly heterogeneous chronic inflammatory disorder, primarily affecting the gastrointestinal tract. Genetic and functional studies have highlighted a key role for innate immunity in its pathogenesis. Profound systemic defects in innate immunity and acute inflammation are understood to result in markedly delayed clearance of bacteria from the tissues, leading to local chronic granulomatous inflammation and compensatory adaptive immunological changes. Macrophages, key orchestrators of acute inflammation, are likely to play an important role in the initial impaired innate immune response. Monocyte-derived macrophages from CD patients stimulated with Escherichia coli were shown to release attenuated levels of tumour necrosis factor and interferon-γ with normal secretion of interleukin-8 (IL-8), IL-10 and IL-6. In controls, the secretion of these cytokines was strongly positively correlated, which was not seen with CD macrophages. The transcriptomes of CD and control macrophages were examined in an attempt to understand the molecular basis of this defect. There were no differentially expressed genes identified between the two groups, consistent with genetic heterogeneity; however, a number of molecules were found to be under-expressed in subgroups of CD patients. The most common of these was optineurin (OPTN) which was under-expressed in approximately 10% of the CD patients. Reduced OPTN expression coincided with lower intracellular protein levels and diminished cytokine secretion after bacterial stimulation both in the patients and with small interfering RNA knockdown in THP-1 cells. Identifying and studying subgroups of patients with shared defective gene expression could aid our understanding of the mechanisms underlying highly heterogeneous diseases such as CD.
克罗恩病(CD)是一种复杂且高度异质性的慢性炎症性疾病,主要累及胃肠道。基因和功能研究突显了固有免疫在其发病机制中的关键作用。固有免疫和急性炎症方面的严重全身性缺陷被认为会导致细菌从组织中的清除明显延迟,进而引发局部慢性肉芽肿性炎症和代偿性适应性免疫变化。巨噬细胞是急性炎症的关键协调者,可能在初始受损的固有免疫反应中发挥重要作用。用大肠杆菌刺激CD患者的单核细胞衍生巨噬细胞后,发现其肿瘤坏死因子和干扰素-γ的释放水平降低,而白细胞介素-8(IL-8)、IL-10和IL-6的分泌正常。在对照组中,这些细胞因子的分泌呈强正相关,而CD巨噬细胞则未出现这种情况。对CD和对照巨噬细胞的转录组进行了检测,以试图了解这种缺陷的分子基础。两组之间未发现差异表达基因,这与基因异质性一致;然而,发现一些分子在CD患者亚组中表达下调。其中最常见的是发动蛋白(OPTN),约10%的CD患者中其表达下调。在患者以及经小干扰RNA敲低的THP-1细胞中,OPTN表达降低与细菌刺激后细胞内蛋白质水平降低和细胞因子分泌减少同时出现。识别和研究具有共同缺陷基因表达的患者亚组有助于我们理解诸如CD等高度异质性疾病的潜在机制。