General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.
Rheumatology, University Hospitals Leuven, Leuven, Belgium; KU Leuven Department of Development and Regeneration, Skeletal Biology and Engineering Research Centre, Laboratory of Tissue Homeostasis and Disease.
Semin Arthritis Rheum. 2021 Apr;51(2):486-494. doi: 10.1016/j.semarthrit.2021.03.012. Epub 2021 Mar 27.
Myositis-specific autoantibodies (MSAs) are thought to be mutually exclusive in patients with idiopathic inflammatory myopathies (IIM) based on studies with immunoprecipitation-based (IP) detection methods. Recently, detection of multiple MSAs in unique patients is increasingly reported, but the extent of this phenomenon remains unclear.
At our centre, we reviewed results from two line immunoassays and one dot immunoassay in 145 IIM patients and 240 controls for the presence of multiple MSAs. Pubmed and Embase were systematically searched for articles mentioning detection of multiple MSAs in IIM patients, published until February 2019. We assessed the frequency, detection method, the precise combinations and clinical phenotypes of participants with multiple MSAs.
At our centre, detection of multiple MSAs occurred in 3.4-8.3% of patients with IIM, depending on the assay. However, no cases with full concordance across all three assays were identified. Forty-four articles reported detection of multiple MSAs, representing a total of 133 cases, including four patients with a connective tissue disease other than IIM and two healthy controls. In 101 cases all MSAs were detected using only one detection method: 40 cases with IP-based methods (most frequently used technique) and 61 cases with other assay types. In most cases the phenotype of patients with multiple MSAs matched the predicted presentation associated with one MSA and in few cases the phenotype matched with both MSAs.
Detection of multiple MSAs in unique IIM patients is less rare than commonly accepted. Specificity issues of the commercially available multiplex immunoassays may, at least partly, explain the higher frequency compared to IP-based methods. 'True multiple MSA-positive' patients may exist, though they are most likely rare.
基于免疫沉淀法(IP)检测方法的研究表明,特发性炎性肌病(IIM)患者的肌炎特异性自身抗体(MSAs)相互排斥。最近,越来越多报道了在独特的患者中检测到多种 MSAs,但这种现象的程度尚不清楚。
在我们中心,我们回顾了 145 例 IIM 患者和 240 例对照者的两种线免疫分析和一种斑点免疫分析的结果,以确定是否存在多种 MSAs。我们系统地检索了 Pubmed 和 Embase 上提到在 IIM 患者中检测到多种 MSAs 的文章,检索截至 2019 年 2 月。我们评估了具有多种 MSAs 的参与者的频率、检测方法、确切的组合和临床表型。
在我们中心,根据检测方法的不同,IIM 患者中检测到多种 MSAs 的频率为 3.4%-8.3%。然而,在所有三种检测方法中均未发现完全一致的病例。44 篇文章报道了多种 MSAs 的检测,共涉及 133 例,包括 4 例结缔组织病以外的 IIM 患者和 2 例健康对照者。在 101 例中,所有 MSAs 仅使用一种检测方法检测到:40 例使用基于 IP 的方法(最常用的技术)和 61 例使用其他检测类型。在大多数情况下,具有多种 MSAs 的患者的表型与一种 MSA 相关的预测表现相匹配,在少数情况下与两种 MSAs 相匹配。
在独特的 IIM 患者中检测到多种 MSAs 并不罕见。与基于 IP 的方法相比,商业上可用的多重免疫分析的特异性问题可能至少部分解释了这种较高的频率。可能存在真正的多种 MSA 阳性患者,但他们很可能很少见。