Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia School of Medicine, Charlottesville, VA, USA.
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA.
Sci Rep. 2024 Jun 3;14(1):12668. doi: 10.1038/s41598-024-63299-y.
Crohn's disease is an inflammatory condition of the intestine characterized by largely unknown etiology and a relapse remission cycle of disease control. While possible triggers have been identified, research is inconsistent on the precise cause of these relapses, especially in the under-researched pediatric population. We hypothesized that patients in remission would have persistent microbial and inflammatory changes in small intestinal tissue that might trigger relapse. To this end, we analyzed intestinal biopsy samples from six patients with pediatric Crohn's disease in remission and a control group of 16 pediatric patients with no evident pathogenic abnormality. We identified compositional microbiota differences, including decreases in the genera Streptococcus and Actinobacillus as well as increases in Oribacterium and Prevotella in patients with controlled Crohn's disease compared to controls. Further, a histologic analysis found that patients with controlled Crohn's disease had increased epithelial integrity, and decreased intraepithelial lymphocytes compared with controls. Additionally, we observed increased peripheral CD4 T cells in patients with pediatric Crohn's disease. These results indicate that markers of intestinal inflammation are responsive to Crohn's disease treatment, however the interventions may not resolve the underlying dysbiosis. These findings suggest that persistent dysbiosis may increase vulnerability to relapse of pediatric Crohn's disease. This study used a nested cohort of patients from the Bangladesh Environmental Enteric Dysfunction (BEED) study (ClinicalTrials.gov ID: NCT02812615 Date of first registration: 24/06/2016).
克罗恩病是一种肠道炎症性疾病,其病因在很大程度上尚不清楚,且具有疾病控制的复发缓解周期。虽然已经确定了一些可能的诱因,但对于这些复发的确切原因的研究仍存在不一致,尤其是在研究较少的儿科人群中。我们假设缓解期的患者在小肠组织中仍存在持续的微生物和炎症变化,这可能会引发疾病复发。为此,我们分析了 6 名处于缓解期的儿科克罗恩病患者和 16 名无明显致病异常的儿科对照患者的肠道活检样本。我们发现了组成微生物群的差异,包括与对照组相比,控制组克罗恩病患者的链球菌属和放线杆菌属减少,而卵形菌属和普雷沃氏菌属增加。此外,组织学分析发现,与对照组相比,处于缓解期的克罗恩病患者具有更高的上皮完整性和更少的上皮内淋巴细胞。此外,我们观察到儿科克罗恩病患者的外周血 CD4+T 细胞增加。这些结果表明,肠道炎症标志物对克罗恩病的治疗有反应,但干预措施可能无法解决潜在的菌群失调。这些发现表明,持续的菌群失调可能会增加儿科克罗恩病复发的易感性。本研究使用了孟加拉国环境肠功能障碍(BEED)研究的嵌套队列患者(临床试验.gov 标识符:NCT02812615,首次注册日期:2016 年 6 月 24 日)。