Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York; Henry D. Janowitz Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Gastroenterology. 2023 Apr;164(4):619-629. doi: 10.1053/j.gastro.2022.12.042. Epub 2023 Jan 10.
BACKGROUND & AIMS: Better biomarkers for prediction of ulcerative colitis (UC) development and prognostication are needed. Anti-integrin αvβ6 (anti-αvβ6) autoantibodies have been described in patients with UC. We tested for the presence of anti-αvβ6 antibodies in the preclinical phase of UC and studied their association with disease-related outcomes after diagnosis.
Anti-αvβ6 autoantibodies were measured in 4 longitudinal serum samples collected from 82 subjects who later developed UC and 82 matched controls from a Department of Defense preclinical cohort (PREDICTS [Proteomic Evaluation and Discovery in an IBD Cohort of Tri-service Subjects]). In a distinct, external validation cohort (Crohn's and Colitis Canada Genetic Environmental Microbial project cohort), we tested 12 pre-UC subjects and 49 matched controls. Furthermore, anti-αvβ6 autoantibodies were measured in 2 incident UC cohorts (COMPASS [Comprehensive Care for the Recently Diagnosed IBD Patients], n = 55 and OSCCAR [Ocean State Crohn's and Colitis Area Registry], n = 104) and associations between anti-αvβ6 autoantibodies and UC-related outcomes were defined using Cox proportional hazards model.
Anti-αvβ6 autoantibodies were significantly higher among individuals who developed UC compared with controls up to 10 years before diagnosis in PREDICTS. The anti-αvβ6 autoantibody seropositivity was 12.2% 10 years before diagnosis and increased to 52.4% at the time of diagnosis in subjects who developed UC compared with 2.7% in controls across the 4 time points. Anti-αvβ6 autoantibodies predicted UC development with an area under the curve of at least 0.8 up to 10 years before diagnosis. The presence of anti-αvβ6 autoantibodies in preclinical UC samples was validated in the GEM cohort. Finally, high anti-αvβ6 autoantibodies was associated with a composite of adverse UC outcomes, including hospitalization, disease extension, colectomy, systemic steroid use, and/or escalation to biologic therapy in recently diagnosed UC.
Anti-integrin αvβ6 autoantibodies precede the clinical diagnosis of UC by up to 10 years and are associated with adverse UC-related outcomes.
需要更好的生物标志物来预测溃疡性结肠炎(UC)的发展和预后。在 UC 患者中已经描述了抗整合素 αvβ6(抗-αvβ6)自身抗体。我们在 UC 的临床前阶段检测了抗-αvβ6 抗体的存在,并研究了它们与诊断后疾病相关结局的关系。
在来自国防部临床前队列(PREDICTS [IBD 受试者的蛋白质组学评估和发现])的 82 例后来发展为 UC 的患者和 82 例匹配对照者的 4 个纵向血清样本中测量了抗-αvβ6 自身抗体。在一个独立的外部验证队列(克罗恩病和结肠炎加拿大遗传环境微生物项目队列)中,我们测试了 12 例 UC 前患者和 49 例匹配对照者。此外,在 2 个新发病例 UC 队列(COMPASS [最近诊断为 IBD 患者的综合护理],n=55 和 OSCCAR [Ocean State Crohn's 和 Colitis Area Registry],n=104)中测量了抗-αvβ6 自身抗体,并使用 Cox 比例风险模型定义了抗-αvβ6 自身抗体与 UC 相关结局之间的关系。
与对照组相比,在 PREDICTS 中,在诊断前长达 10 年的时间里,发展为 UC 的个体的抗-αvβ6 自身抗体明显更高。在发展为 UC 的受试者中,抗-αvβ6 自身抗体的血清阳性率在诊断前 10 年为 12.2%,在诊断时增加到 52.4%,而在 4 个时间点的对照组中为 2.7%。在诊断前长达 10 年的时间里,抗-αvβ6 自身抗体预测 UC 发展的曲线下面积至少为 0.8。在 GEM 队列中验证了临床前 UC 样本中存在抗-αvβ6 自身抗体。最后,高抗-αvβ6 自身抗体与最近诊断为 UC 的患者中不良 UC 结局的复合事件(包括住院、疾病扩展、结肠切除术、全身皮质类固醇使用和/或升级为生物治疗)相关。
抗整合素 αvβ6 自身抗体在 UC 的临床诊断前长达 10 年出现,并与不良的 UC 相关结局相关。