Williams Amanda D, Korolkova Olga Y, Sakwe Amos M, Geiger Timothy M, James Samuel D, Muldoon Roberta L, Herline Alan J, Goodwin J Shawn, Izban Michael G, Washington Mary K, Smoot Duane T, Ballard Billy R, Gazouli Maria, M'Koma Amosy E
Department of Microbiology and Immunology, Meharry Medical College School of Medicine, Nashville, Tennessee, United States of America.
Department of Biology, Lipscomb University, Nashville, Tennessee, United States of America.
PLoS One. 2017 Aug 17;12(8):e0179710. doi: 10.1371/journal.pone.0179710. eCollection 2017.
Inability to distinguish Crohn's colitis from ulcerative colitis leads to the diagnosis of indeterminate colitis. This greatly effects medical and surgical care of the patient because treatments for the two diseases vary. Approximately 30 percent of inflammatory bowel disease patients cannot be accurately diagnosed, increasing their risk of inappropriate treatment. We sought to determine whether transcriptomic patterns could be used to develop diagnostic biomarker(s) to delineate inflammatory bowel disease more accurately. Four patients groups were assessed via whole-transcriptome microarray, qPCR, Western blot, and immunohistochemistry for differential expression of Human α-Defensin-5. In addition, immunohistochemistry for Paneth cells and Lysozyme, a Paneth cell marker, was also performed. Aberrant expression of Human α-Defensin-5 levels using transcript, Western blot, and immunohistochemistry staining levels was significantly upregulated in Crohn's colitis, p< 0.0001. Among patients with indeterminate colitis, Human α-Defensin-5 is a reliable differentiator with a positive predictive value of 96 percent. We also observed abundant ectopic crypt Paneth cells in all colectomy tissue samples of Crohn's colitis patients. In a retrospective study, we show that Human α-Defensin-5 could be used in indeterminate colitis patients to determine if they have either ulcerative colitis (low levels of Human α-Defensin-5) or Crohn's colitis (high levels of Human α-Defensin-5). Twenty of 67 patients (30 percent) who underwent restorative proctocolectomy for definitive ulcerative colitis were clinically changed to de novo Crohn's disease. These patients were profiled by Human α-Defensin-5 immunohistochemistry. All patients tested strongly positive. In addition, we observed by both hematoxylin and eosin and Lysozyme staining, a large number of ectopic Paneth cells in the colonic crypt of Crohn's colitis patient samples. Our experiments are the first to show that Human α-Defensin-5 is a potential candidate biomarker to molecularly differentiate Crohn's colitis from ulcerative colitis, to our knowledge. These data give us both a potential diagnostic marker in Human α-Defensin-5 and insight to develop future mechanistic studies to better understand crypt biology in Crohn's colitis.
无法区分克罗恩病性结肠炎和溃疡性结肠炎会导致诊断为不确定性结肠炎。这对患者的医疗和手术护理有很大影响,因为这两种疾病的治疗方法不同。大约30%的炎症性肠病患者无法得到准确诊断,从而增加了接受不恰当治疗的风险。我们试图确定转录组模式是否可用于开发诊断生物标志物,以更准确地界定炎症性肠病。通过全转录组微阵列、定量聚合酶链反应、蛋白质免疫印迹和免疫组织化学对四组患者进行评估,以检测人α-防御素-5的差异表达。此外,还对潘氏细胞和潘氏细胞标志物溶菌酶进行了免疫组织化学检测。利用转录本、蛋白质免疫印迹和免疫组织化学染色水平检测,发现人α-防御素-5在克罗恩病性结肠炎中的异常表达显著上调,p<0.0001。在不确定性结肠炎患者中,人α-防御素-5是一种可靠的鉴别指标,阳性预测值为96%。我们还在所有克罗恩病性结肠炎患者的结肠切除组织样本中观察到大量异位隐窝潘氏细胞。在一项回顾性研究中,我们表明人α-防御素-5可用于不确定性结肠炎患者,以确定他们患的是溃疡性结肠炎(人α-防御素-5水平低)还是克罗恩病性结肠炎(人α-防御素-5水平高)。67例因明确的溃疡性结肠炎接受保留肛门的结肠直肠切除术的患者中有20例(30%)临床上被重新诊断为新发克罗恩病。通过人α-防御素-5免疫组织化学对这些患者进行分析。所有检测患者均呈强阳性。此外,通过苏木精-伊红染色和溶菌酶染色,我们在克罗恩病性结肠炎患者样本的结肠隐窝中观察到大量异位潘氏细胞。据我们所知,我们的实验首次表明人α-防御素-5是从分子水平区分克罗恩病性结肠炎和溃疡性结肠炎的潜在候选生物标志物。这些数据为我们提供了人α-防御素-5这一潜在诊断标志物,并为开展未来的机制研究提供了思路,以便更好地理解克罗恩病性结肠炎中的隐窝生物学。