Associated Regional and University Pathologists (ARUP) Institute for Clinical and Experimental Pathology, USA.
J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):19-23. doi: 10.1097/MPG.0b013e3181c992be.
: Several serologic assays are commercially available to aid in the diagnosis of gluten-sensitive enteropathy (GSE). Our objective in this study was to assess the performance of a novel combined antigen-screening assay for GSE.
: Deidentified sera from 111 pediatric patients suspected of having celiac disease (CD), 130 adults diagnosed with dermatitis herpetiformis (DH), and 77 pediatric and 49 adult normal controls were included in the study. Sera from 10 patients submitted to our laboratory for GSE testing with IgA deficiency and IgG antibodies against 1 or more of the traditional serologic markers associated with GSE were also included. All sera were screened for antibodies (IgA and IgG) against tissue transglutaminase (tTG) and deamidated gliadin peptides (DGP) by enzyme immunoassay (EIA) in a single test well. In addition, all sera were assessed for each individual marker and isotype using separate EIAs.
: The IgA/IgG anti-tTG/DGP EIA screen was 92.6% sensitive and 94.3% specific in pediatric CD and detected 1 patient (Marsh 3c) who was IgA anti-tTG negative; this patient was not IgA deficient (<7.0 mg/dL). All 10 IgA-deficient sera gave positive results by the tTG/DGP EIA screen. Sensitivity and specificity of the tTG/DGP EIA screen in retrospective and prospective DH were 65% and 100% versus 62% and 100%, respectively.
: The new IgA/IgG anti-tTG/DGP EIA screen was slightly more sensitive than IgA anti-tTG alone in pediatric CD. This novel screening assay may allow the current recommendation of measuring total serum IgA in suspected GSE patients to be eliminated.
有几种血清学检测方法可用于辅助诊断麸质敏感性肠病(GSE)。本研究旨在评估一种新型联合抗原筛查检测方法在 GSE 中的应用。
本研究纳入了 111 例疑似乳糜泻(CD)的儿科患者、130 例确诊为疱疹样皮炎(DH)的成年患者、77 例儿科和 49 例成年正常对照的血清。还纳入了 10 例因 GSE 检测而提交至本实验室的患者血清,这些患者存在 IgA 缺乏和针对 1 种或多种与 GSE 相关的传统血清学标志物的 IgG 抗体。所有血清均通过酶联免疫吸附试验(EIA)在单个检测孔中筛查针对组织转谷氨酰胺酶(tTG)和脱酰胺麦胶肽(DGP)的抗体(IgA 和 IgG)。此外,所有血清均通过单独的 EIA 评估每种单独的标志物和同种型。
在儿科 CD 中,IgA/IgG 抗 tTG/DGP EIA 筛查的敏感性为 92.6%,特异性为 94.3%,并检测到 1 例 IgA 抗 tTG 阴性(Marsh 3c)的患者;该患者未发生 IgA 缺乏症(<7.0mg/dL)。所有 10 例 IgA 缺乏症患者的 tTG/DGP EIA 筛查结果均为阳性。在回顾性和前瞻性 DH 中,tTG/DGP EIA 筛查的敏感性和特异性分别为 65%和 100%,以及 62%和 100%。
新型 IgA/IgG 抗 tTG/DGP EIA 筛查在儿科 CD 中的敏感性略高于单独的 IgA 抗 tTG。这种新型筛查检测方法可能使目前推荐在疑似 GSE 患者中检测总血清 IgA 的建议得以消除。