Department of Gastroenterology, The Cleveland Clinic Foundation, Cleveland, OH, USA.
J Crohns Colitis. 2011 Dec;5(6):570-6. doi: 10.1016/j.crohns.2011.05.011. Epub 2011 Jun 24.
Inflammatory bowel disease (IBD) is reported to be associated with autoimmune pancreatitis. The aim of the study was to investigate serum IgG4 and tissue infiltration of IgG4+ plasma cells in symptomatic patients with ileal pouches.
Ninety-seven consecutive persistent symptomatic patients with ileal pouches from our subspecialty Pouchitis Clinic from January to December 2010 were included in the study. Serum IgG4 was measured at the time of presentation. All patients underwent pouchoscopy with pouch biopsies immunostained for IgG4+ plasma cells. Patients with ≥10 per high-power field of IgG4+ plasma cells were considered positive for the stain.
Twenty-eight (28.9%) patients had positive IgG4 immunostaining of pouch and/or afferent limb biopsy, while the remaining 69 patients (71.1%) were IgG4 negative. Demographic and symptoms were similar between the two groups. The median serum IgG4 in the IgG4 positive group was 21.3 (interquartile range 0-41.3) mg/dL vs. 0 (interquartile range 0-18) in the IgG4 negative group. (p=0.04). On multivariate analysis, the Pouchitis Disease Activity Index (PDAI) endoscopy score in the pouch (odds ratio [OR] 1.66, 95% confidence interval [CI]: 1.21-2.29, p=0.002) and number of concomitant autoimmune disorders (OR 3.04, 95% CI: 1.22-7.53, p=0.017) were independent risk factors for the presence of IgG4+ plasma cell infiltration.
Increased IgG4+ plasma cells were found in 1/4 of IPAA patients with persistent symptoms. The presence of tissue infiltration of IgG4+ plasma cells appeared to be associated with chronic pouch inflammation and concurrent autoimmune disorders.
炎症性肠病(IBD)与自身免疫性胰腺炎有关。本研究旨在研究有症状的回肠袋患者的血清 IgG4 和 IgG4+浆细胞浸润。
2010 年 1 月至 12 月,我们的 pouchitis 诊所连续纳入 97 例有持续性症状的回肠袋患者进行研究。在就诊时测量血清 IgG4。所有患者均接受 pouchoscopy 检查,并对 IgG4+浆细胞进行 pouch 活检免疫染色。如果每高倍视野中 IgG4+浆细胞≥10 个,则认为该染色为阳性。
28 例(28.9%)患者的 pouch 和/或输入襻活检有 IgG4 免疫染色阳性,而其余 69 例(71.1%)患者 IgG4 阴性。两组患者的人口统计学和症状相似。IgG4 阳性组的血清 IgG4 中位数为 21.3(四分位距 0-41.3)mg/dL,而 IgG4 阴性组为 0(四分位距 0-18)mg/dL。(p=0.04)。在多变量分析中,pouch 中的 Pouchitis Disease Activity Index(PDAI)内镜评分(比值比 [OR] 1.66,95%置信区间 [CI]:1.21-2.29,p=0.002)和同时存在的自身免疫性疾病数量(OR 3.04,95% CI:1.22-7.53,p=0.017)是 IgG4+浆细胞浸润存在的独立危险因素。
1/4 有持续性症状的 IPAA 患者发现 IgG4+浆细胞增多。组织 IgG4+浆细胞浸润的存在似乎与慢性 pouch 炎症和同时存在的自身免疫性疾病有关。