Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.
Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium.
Neurogastroenterol Motil. 2019 Apr;31(4):e13542. doi: 10.1111/nmo.13542. Epub 2019 Jan 18.
The role of persistent immune activation in postinfectious irritable bowel syndrome (PI-IBS) remains controversial. Here, we prospectively studied healthy subjects traveling to destinations with a high-risk to develop infectious gastroenteritis (IGE) in order to identify immune-mediated mechanisms and risk factors of PI-IBS.
One hundred and one travelers were asked to complete questionnaires on psychological profile and gastrointestinal (GI) symptoms before travel, 2 weeks, 6 months and 1 year after travel. At each visit, blood was collected for PBMC isolation and rectal biopsies were taken. PI-IBS was diagnosed using the Rome III criteria and subjects with persistent postinfectious abdominal complaints (PI-AC) were identified using 3 GSRS symptoms (ie, loose stools, urgency and abdominal pain).
Forty-seven of the 101 subjects reported IGE during travel. After 1 year, two subjects were diagnosed with PI-IBS and eight subjects were presented with PI-AC versus two subjects with IBS and two with abdominal complaints in the non-infected group. PBMC analysis showed no differences in T and B cell populations in subjects with PI-AC vs healthy. Additionally, no differences in gene expression were observed in the early postinfectious phase or after 1 year. Regression analysis identified looser stools, higher anxiety and somatization before infection and several postinfectious GI symptoms as risk factors for PI-AC.
The incidence of PI-IBS is low following travelers' diarrhea and there is need for larger studies investigating the role of immune activation in PI-IBS. Psychological factors before infection and the severity of symptoms shortly after infection are risk factors for the persistence of PI-AC.
持续性免疫激活在感染后肠易激综合征(PI-IBS)中的作用仍存在争议。在这里,我们前瞻性地研究了前往感染性胃肠炎(IGE)高风险目的地的健康旅行者,以确定 PI-IBS 的免疫介导机制和危险因素。
101 名旅行者在旅行前、旅行后 2 周、6 个月和 1 年时被要求完成心理特征和胃肠道(GI)症状的问卷。每次就诊时,采集 PBMC 分离的血液和直肠活检。使用 Rome III 标准诊断 PI-IBS,使用 3 项 GSRS 症状(即稀便、急迫和腹痛)识别持续性感染后腹部症状(PI-AC)。
101 名受试者中有 47 名报告在旅行中发生 IGE。1 年后,2 名受试者被诊断为 PI-IBS,8 名受试者出现 PI-AC,而非感染组中 2 名受试者出现 IBS,2 名受试者出现腹部不适。PBMC 分析显示,PI-AC 与健康对照组的 T 和 B 细胞群无差异。此外,在早期感染后或 1 年后,未观察到基因表达的差异。回归分析确定感染前更稀便、更高的焦虑和躯体化以及感染后数种 GI 症状是 PI-AC 的危险因素。
旅行者腹泻后 PI-IBS 的发病率较低,需要更大规模的研究来探讨免疫激活在 PI-IBS 中的作用。感染前的心理因素和感染后症状的严重程度是 PI-AC 持续存在的危险因素。