免疫测定法检测血清阴性原发性干燥综合征患者唾液中的抗SSA/Ro-52自身抗体。

Sarah Kamounah, Nabihah Tayob, Samantha Chiang, Fang Wei, Jin Kyun Park, Hyun Mi Kwon, Ziding Feng, David Chia, Anne Marie Lynge Pedersen, Yeong Wook Song, David T W Wong
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引用次数: 0

摘要

干燥综合征的诊断工作具有挑战性和复杂性,包括检测SSA/Ro的血清自身抗体和唇唾液腺活检。此外,诊断往往会延迟。在这项研究中,我们检验了这样一种假设,即在原发性干燥综合征(pSS)患者的唾液中可以检测到抗SSA/Ro自身抗体,因为该疾病会影响唾液腺,并且这些自身抗体在唾液中比在血清中表现出更大的辨别能力。SSA/Ro-52Ags被用于开发一种新的基于电化学的定量免疫分析:电场诱导释放和测量(EFIRM)平台。通过测量患有pSS和sicca的患者(n=34)、患有sicca的非pSS患者(n=35)和健康受试者(n=41)的唾液抗SSA/Ro-52自身抗体来确定临床效用。判别的统计分析包括接收器工作特性曲线下的面积。94%(32/34)的pSS患者检测到唾液抗SSA/Ro-52自身抗体,85%(29/34)的血清阳性。五名pSS血清阴性患者中有四名在唾液中具有EFIRM可测量的抗SSA/Ro-52自身抗体。此外,在患有sicca的无pSS血清阴性患者中,60%(35人中有21人)的唾液中存在可检测到EFIRM的SSA/Ro-52自身抗体,表明自身免疫性疾病的发作。41名健康对照受试者中有两名唾液中存在可检测到EFIRM的SSA/Ro-52自身抗体。唾液SSA/Ro-52自身抗体显著区分pSS患者或自身免疫性疾病初始阶段患者与受试者操作特征曲线下面积为0.91的健康受试者。我们的研究结果表明,所提出的唾液SSA/Ro-52免疫测定提高了对pSS血清阴性患者和早发性自身免疫性疾病患者的早期准确诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunoassay Detects Salivary Anti-SSA/Ro-52 Autoantibodies in Seronegative Patients with Primary Sjögren's Syndrome.

Immunoassay Detects Salivary Anti-SSA/Ro-52 Autoantibodies in Seronegative Patients with Primary Sjögren's Syndrome.

Immunoassay Detects Salivary Anti-SSA/Ro-52 Autoantibodies in Seronegative Patients with Primary Sjögren's Syndrome.

Immunoassay Detects Salivary Anti-SSA/Ro-52 Autoantibodies in Seronegative Patients with Primary Sjögren's Syndrome.

The diagnostic work-up for Sjögren's syndrome is challenging and complex, including testing for serum autoantibodies to SSA/Ro and a labial salivary gland biopsy. Furthermore, the diagnosis is often delayed. In this study, we tested the hypothesis that anti-SSA/Ro autoantibodies are detectable in the saliva of patients with primary Sjögren's syndrome (pSS) because the disease affects the salivary glands, and these autoantibodies display greater discriminatory performance in saliva than in serum. SSA/Ro-52 Ags were used to develop what is, to our knowledge, a novel quantitative electrochemical-based immunoassay: the electric field-induced release and measurement (EFIRM) platform. The clinical utility was determined by measuring salivary anti-SSA/Ro-52 autoantibodies in patients with pSS and sicca (n = 34), patients without pSS with sicca (n = 35), and healthy subjects (n = 41). The statistical analysis of discrimination included the area under the receiver operating characteristic curve. Salivary anti-SSA/Ro-52 autoantibodies were measured in 94% (32 of 34) of patients with pSS with 85% (29 of 34) seropositivity. Four of the five seronegative patients with pSS had EFIRM-measurable anti-SSA/Ro-52 autoantibodies in saliva. Additionally, 60% (21 of 35) of the seronegative patients without pSS who had sicca had EFIRM-detectable SSA/Ro-52 autoantibodies in saliva, indicating the onset of autoimmune disease. Two of the 41 healthy control subjects had EFIRM-detectable SSA/Ro-52 autoantibodies in their saliva. Salivary SSA/Ro-52 autoantibodies significantly discriminated patients with pSS or patients with the initial stage of autoimmune disease from healthy subjects with an area under the receiver operating characteristic curve of 0.91. Our findings suggest that the proposed saliva SSA/Ro-52 immunoassay improves early and accurate diagnosis of seronegative patients with pSS and patients with early-onset autoimmune disease.

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