Gastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), 28006 Madrid, Spain.
Área de Farmacología y Nutrición y Bromatología, Grupo de Investigación de Alto Rendimiento en Fisiopatología del Sistema Digestivo URJC: NeuGut-URJC, Departamento Ciencias Básicas de la Salud, Universidad Rey Juan Carlos, 28922 Madrid, Spain.
Int J Mol Sci. 2023 Oct 28;24(21):15691. doi: 10.3390/ijms242115691.
Biological therapies only benefit one-third of patients with Crohn's disease (CD). For this reason, a deeper understanding of the mechanisms by which biologics elicit their effect on intestinal mucosa is needed. Increasing evidence points toward the involvement of long noncoding RNAs (lncRNAs) in the pathogenesis of CD, although their role remains poorly studied. We aimed to characterize lncRNA profiles in the ileum and colon from CD patients and evaluate the effect of anti-TNF-α treatment on their transcription. Terminal ileum and left colon samples from 30 patients (active CD = 10, quiescent CD = 10, and healthy controls (HCs) = 10) were collected for RNA-seq. The patients were classified according to endoscopic activity. Furthermore, biopsies were cultured with infliximab, and their transcriptome was determined by Illumina gene expression array. A total of 678 differentially expressed lncRNAs between the terminal ileum and left colon were identified in HCs, 438 in patients with quiescent CD, and 468 in patients with active CD. Additionally, we identified three new lncRNAs in the ileum associated with CD activity. No differences were observed when comparing the effect of infliximab according to intestinal location, presence of disease (CD vs. HC), and activity (active vs. quiescent). The expression profiles of lncRNAs are associated with the location of intestinal tissue, being very different in the ileum and colon. The presence of CD and disease activity are associated with the differential expression of lncRNAs. No modulatory effect of infliximab has been observed in the lncRNA transcriptome.
生物疗法仅使三分之一的克罗恩病(CD)患者受益。因此,需要更深入地了解生物制剂对肠道黏膜产生作用的机制。越来越多的证据表明长链非编码 RNA(lncRNA)参与了 CD 的发病机制,尽管它们的作用仍未得到充分研究。我们旨在描述 CD 患者回肠和结肠中的 lncRNA 谱,并评估抗 TNF-α治疗对其转录的影响。收集 30 名患者(活动期 CD = 10 名,缓解期 CD = 10 名,健康对照(HCs)= 10 名)的回肠末端和左结肠样本进行 RNA-seq。根据内镜活动对患者进行分类。此外,对活检进行英夫利昔单抗培养,并通过 Illumina 基因表达阵列确定其转录组。在 HCs 中鉴定出 678 个回肠和左结肠之间差异表达的 lncRNA,在缓解期 CD 患者中鉴定出 438 个,在活动期 CD 患者中鉴定出 468 个。此外,我们在与 CD 活性相关的回肠中鉴定出三个新的 lncRNA。当根据肠道位置、疾病存在(CD 与 HCs)和活性(活动期与缓解期)比较英夫利昔单抗的作用时,没有观察到差异。lncRNA 表达谱与肠道组织的位置有关,在回肠和结肠中差异很大。CD 的存在和疾病活动与 lncRNA 的差异表达有关。英夫利昔单抗对 lncRNA 转录组没有调节作用。