Isolated anti-SS-B (La) antibodies: rare occurrence and lack of diagnostic value.

IF 4.7 2区 医学 Q1 RHEUMATOLOGY RMD Open Pub Date : 2025-02-04 DOI:10.1136/rmdopen-2024-005212
Paul Cioni, Pascale Chretien, Claire Goulvestre, Eric Ballot, Dounia Khelifi-Touhami, Xavier Mariette, Gaëtane Nocturne
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Abstract

Objective: Anti-SS-B antibodies are often associated with anti-SS-A in Sjögren's disease. Compared to anti-SS-A antibody positivity, the significance of the immunological profile anti-SS-B positive/anti-SS-A negative remains controversial. We aimed to evaluate the prevalence and diagnostic significance of isolated anti-SS-B antibodies.

Methods: We conducted a retrospective study across three hospitals of the Assistance Publique-Hôpitaux de Paris. Patients with anti-SS-B positivity were identified using ELISA, addressable laser beam immunoassay (ALBIA) and immunodot assays. They were retained if anti-SS-B was positive in two techniques and anti-SS-A was absent. Clinical, biological and immunological data were extracted and presented in a descriptive analysis.

Results: A total of 80 540 requests for anti-SS-B antibody testing were carried out over a period of 7.9 years. Anti-SS-B positivity was found in 1693 patients. Among them, 335 (19.8%) patients had isolated anti-SS-B in ELISA/ALBIA. Immunodot was performed in 186 of them and confirmed anti-SS-B positivity in 61 patients (3.6% of anti-SS-B positivity). 24 patients (39.3%) presented with a history of various autoimmune or autoinflammatory diseases and only 6 were diagnosed with a new connective tissue disease. After a median follow-up of 26 months, only two new diagnoses were made.

Conclusion: Anti-SS-B without anti-SS-A is exceedingly rare when accurately identified by a rigorous immunological approach. The initial anti-SS-B positivity does not correlate with a specific condition, both at the time of initial identification and after a 26-month follow-up period. This supports the fact that isolated anti-SS-B has no diagnostic or prognostic value.

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分离的抗ss - b (La)抗体:罕见且缺乏诊断价值。
目的:在Sjögren疾病中,抗ss - b抗体常与抗ss - a抗体相关。与抗ss - a抗体阳性相比,免疫谱抗ss - b阳性/抗ss - a阴性的意义仍存在争议。我们的目的是评估分离的抗ss - b抗体的患病率和诊断意义。方法:我们对巴黎Publique-Hôpitaux援助的三家医院进行了回顾性研究。采用ELISA、可寻址激光束免疫分析法(ALBIA)和免疫点法对抗ss - b阳性患者进行鉴定。如果抗ss - b在两种技术中均呈阳性,而抗ss - a缺失,则保留它们。临床、生物学和免疫学数据被提取并以描述性分析的方式呈现。结果:7.9年共检测ss - b抗体80 540份。抗- ss - b阳性1693例。其中335例(19.8%)患者在ELISA/ALBIA中分离出抗ss - b。其中186例患者行免疫点检测,61例患者血清ss - b抗体阳性(阳性率3.6%)。24例患者(39.3%)有各种自身免疫性或自身炎症病史,仅有6例诊断为新发结缔组织病。在平均随访26个月后,只有两例新诊断。结论:通过严格的免疫学方法准确鉴定出无抗ss - a的抗ss - b抗体是极为罕见的。最初的抗ss - b阳性与特定情况无关,无论是在最初鉴定时还是在26个月的随访期后。这支持了分离抗ss - b没有诊断或预后价值的事实。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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