INOVA Diagnostics, INC. San Diego, CA 32131-1638, USA.
Autoimmun Rev. 2012 Jul;11(9):642-5. doi: 10.1016/j.autrev.2011.11.005. Epub 2011 Nov 11.
The presence of anti-nuclear antibodies (ANA) is a hallmark of systemic autoimmune rheumatic diseases (SARD). The indirect immunofluorescence (IIF) assay on HEp-2 cells is a commonly used test for the detection of ANA and was recently recommended as the screening test of choice by a task force of the American College of Rheumatology. However, up to 20% of serum samples from healthy individuals (HI) have been reported to have a positive ANA test, the majority of which are directed to the dense fine speckles 70 (DFS70) antigen. Even more important, the DFS IIF pattern has been reported in 33% of ANA positive HI, but not in ANA positive SARD sera. Since the intended use of the ANA HEp-2 test is to aid in the diagnosis of SARD, the reporting of anti-DFS70 antibodies and their associated pattern (DFS) as a positive test, significantly reduces the specificity and the positive likelihood of the ANA test. This has significant implications for diagnostic algorithms involving the detection of ANA. We summarize the current knowledge of anti-DFS70 antibodies and their impact on ANA testing. We also suggest a test algorithm which considers the DFS pattern and the presence of anti-DFS70 antibodies. In addition, we describe a novel method based on immunoadsorption of anti-DFS70 antibodies, which increases the specificity of the ANA HEp-2 test for SARD and which has the potential to overcome a significant limitation of the ANA HEp-2 assay.
抗核抗体(ANA)的存在是系统性自身免疫性风湿病(SARD)的标志。在 HEp-2 细胞上进行间接免疫荧光(IIF)检测是检测 ANA 的常用方法,最近被风湿病学美国学院的一个工作组推荐为首选的筛选检测方法。然而,高达 20%的健康个体(HI)的血清样本报告ANA 检测呈阳性,其中大多数针对致密细斑点 70(DFS70)抗原。更重要的是,在 33%的 ANA 阳性 HI 中报告了 DFS IIF 模式,但在 ANA 阳性 SARD 血清中没有报告。由于 ANA HEp-2 检测的预期用途是辅助 SARD 的诊断,因此报告抗-DFS70 抗体及其相关模式(DFS)为阳性检测结果,显著降低了 ANA 检测的特异性和阳性可能性。这对涉及 ANA 检测的诊断算法有重大影响。我们总结了抗-DFS70 抗体的当前知识及其对 ANA 检测的影响。我们还建议了一种考虑 DFS 模式和抗-DFS70 抗体存在的测试算法。此外,我们描述了一种基于免疫吸附抗-DFS70 抗体的新方法,该方法提高了 ANA HEp-2 检测对 SARD 的特异性,并有可能克服 ANA HEp-2 检测的一个重大局限性。