Chase R Christopher, Tamim Hani, Sheikh Walaa G El, Clift Kristin, Bruining David, Ha Christina, Farraye Francis A, Hashash Jana G
Division of Internal Medicine, Mayo Clinic, Jacksonville, Florida USA (R. Christopher Chase).
Clinical Research Institute, American University of Beirut Medical Center, Beirut, Lebanon (Hani Tamim, Walaa G. El Sheikh).
Ann Gastroenterol. 2023 Jul-Aug;36(4):423-429. doi: 10.20524/aog.2023.0807. Epub 2023 May 29.
The etiology of inflammatory bowel disease (IBD) is multifactorial and thought to be influenced by inappropriate activation of the gut mucosal immune system. As the only immunoglobulin G (IgG) subclass unable to activate the classical complement cascade, the role of IgG4 in IBD pathophysiology as an immunomodulator is controversial. This study aimed to determine the association of low, normal and high IgG4 levels with the outcomes of IBD patients.
This was a retrospective study of a multisite tertiary care center database evaluating patients with IBD who had an IgG4 level drawn between 2014 and 2021. Subjects were divided into low, normal, and high IgG4 level groups for evaluation of demographic and clinical indicators of IBD activity and severity.
Of 284 patients with IBD, 22 had low (7.7%), 16 high (5.6%), and 246 (86.6%) normal IgG4 levels. There was no difference in IBD subtype, mean age, age at IBD diagnosis, or smoking between the 3 groups. There was no difference in number of hospitalizations (P=0.20), C-reactive protein levels, need for intestinal resection (P=0.85), or presence of primary sclerosing cholangitis (P=0.15), pancreatitis (P=0.70), or perianal disease (P=0.68) between the groups. Significantly more patients in the low IgG4 group had previous exposure to vedolizumab compared to the other groups and more patients in the low IgG4 group received vedolizumab (P=0.04), azathioprine (P=0.04) and prednisone (P=0.03) during the 5-year follow up.
In this study, a low serum IgG4 level was associated with higher rates of vedolizumab, azathioprine, and steroid use.
炎症性肠病(IBD)的病因是多因素的,被认为受肠道黏膜免疫系统不适当激活的影响。作为唯一不能激活经典补体级联反应的免疫球蛋白G(IgG)亚类,IgG4作为免疫调节剂在IBD病理生理学中的作用存在争议。本研究旨在确定低、正常和高IgG4水平与IBD患者结局之间的关联。
这是一项对多中心三级医疗中心数据库的回顾性研究,评估2014年至2021年间检测过IgG4水平的IBD患者。将受试者分为低、正常和高IgG4水平组,以评估IBD活动度和严重程度的人口统计学和临床指标。
在284例IBD患者中,22例(7.7%)IgG4水平低,16例(5.6%)IgG4水平高,246例(86.6%)IgG4水平正常。三组之间的IBD亚型、平均年龄、IBD诊断年龄或吸烟情况无差异。三组之间的住院次数(P=0.20)、C反应蛋白水平、肠道切除需求(P=0.85)或原发性硬化性胆管炎(P=0.15)、胰腺炎(P=0.70)或肛周疾病(P=0.68)的存在情况无差异。与其他组相比,低IgG4组中曾接触过维多珠单抗的患者明显更多,且在5年随访期间,低IgG4组中接受维多珠单抗(P=0.04)、硫唑嘌呤(P=0.04)和泼尼松(P=0.03)治疗的患者更多。
在本研究中,血清IgG4水平低与维多珠单抗、硫唑嘌呤和类固醇的较高使用频率相关。