Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, USA.
Northwestern University Feinberg School of Medicine, Division of Gastroenterology and Hepatology, Chicago, Illinois, USA.
Clin Transl Gastroenterol. 2021 May 12;12(5):e00349. doi: 10.14309/ctg.0000000000000349.
It is unclear how immune perturbations may influence the pathogenesis of idiopathic gastroparesis, a prevalent functional disorder of the stomach which lacks animal models. Several studies have noted altered immune characteristics in the deep gastric muscle layer associated with gastroparesis, but data are lacking for the mucosal layer, which is endoscopically accessible. We hypothesized that immune dysregulation is present in the gastroduodenal mucosa in idiopathic gastroparesis and that specific immune profiles are associated with gastroparesis clinical parameters.
In this cross-sectional prospective case-control study, routine endoscopic biopsies were used for comprehensive immune profiling by flow cytometry, multicytokine array, and gene expression in 3 segments of the stomach and the duodenal bulb. Associations of immune endpoints with clinical parameters of gastroparesis were also explored.
The gastric mucosa displayed large regional variation of distinct immune profiles. Furthermore, several-fold increases in innate and adaptive immune cells were found in gastroparesis. Various immune cell types showed positive correlations with duration of disease, proton pump inhibitor dosing, and delayed gastric emptying.
This initial observational study showed immune compartmentalization of the human stomach mucosa and significant immune dysregulation at the level of leukocyte infiltration in idiopathic gastroparesis patients that extends to the duodenum. Select immune cells, such as macrophages, may correlate with clinicopathological traits of gastroparesis. This work supports further mucosal studies to advance our understanding of gastroparesis pathophysiology.
免疫紊乱如何影响特发性胃轻瘫(一种常见的胃部功能性疾病,缺乏动物模型)的发病机制尚不清楚。几项研究指出,与胃轻瘫相关的胃深层肌肉层存在改变的免疫特征,但缺乏内镜可及的黏膜层的数据。我们假设特发性胃轻瘫患者的胃十二指肠黏膜存在免疫失调,并且特定的免疫特征与胃轻瘫的临床参数相关。
在这项横断面前瞻性病例对照研究中,使用常规内镜活检通过流式细胞术、多细胞因子阵列和胃和十二指肠球部的 3 个部位的基因表达进行全面免疫谱分析。还探讨了免疫终点与胃轻瘫临床参数的相关性。
胃黏膜显示出明显的免疫特征的区域性大变化。此外,胃轻瘫患者的固有和适应性免疫细胞增加了数倍。各种免疫细胞类型与疾病持续时间、质子泵抑制剂剂量和胃排空延迟呈正相关。
这项初步观察性研究显示,人胃黏膜存在免疫区室化,特发性胃轻瘫患者存在明显的免疫失调,延伸至十二指肠。某些免疫细胞,如巨噬细胞,可能与胃轻瘫的临床病理特征相关。这项工作支持进一步的黏膜研究,以推进我们对胃轻瘫发病机制的理解。