Martinsson Klara, Johansson Linda, Kastbom Alf, Rantapää-Dahlqvist Solbritt
Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Department of Public Health and Clinical Medicine/Rheumatology, Umeå University, Umeå, Sweden.
Rheumatology (Oxford). 2025 May 1;64(5):3166-3170. doi: 10.1093/rheumatology/keaf032.
To investigate the occurrence and dynamics of secretory component-containing antibodies towards citrullinated proteins (SC ACPA) in plasma from pre-symptomatic individuals subsequently developing rheumatoid arthritis (RA).
We studied 319 individuals who had donated plasma prior to RA onset (median predating time 4.7 years), whereof 181 also donated samples after diagnosis. One hundred individuals were randomly selected from the same biobank cohorts to serve as controls. SC ACPA, total secretory IgA (TSIgA) and IgG ACPA were analysed in plasma by enzyme-linked immunoassays.
Circulating SC ACPA levels in pre-symptomatic individuals and RA patients were significantly increased compared with controls [median (interquartile range) 108 (108), 179 (248) and 12.5 (537) AU/ml, respectively; P < 0.001], and SC ACPA levels in RA patients were significantly increased compared with pre-symptomatic individuals (P < 0.001). SC ACPA increased, in terms of both levels and proportion of positive samples, closer to symptom onset and diagnosis. TSIgA was not elevated compared with controls either during the pre-dating time or after diagnosis. The earliest detected SC ACPA positive sample was 9 years before symptom onset, as compared with 11 years for IgG ACPA. Only two pre-dating samples were positive for SC ACPA and negative for IgG ACPA.
Circulating SC ACPA responses arise and magnify during the asymptomatic phase of disease development in a subgroup of RA patients. This suggests mucosal involvement prior to both symptom onset and subsequent arthritis. As mirrored in the circulation, however, SC ACPA does not seem to precede the IgG ACPA response.
研究在随后发展为类风湿关节炎(RA)的症状前个体血浆中含分泌成分的抗瓜氨酸化蛋白抗体(SC ACPA)的发生情况及动态变化。
我们研究了319名在RA发病前捐献血浆的个体(中位提前时间4.7年),其中181人在诊断后也捐献了样本。从同一生物样本库队列中随机选取100名个体作为对照。采用酶联免疫吸附测定法分析血浆中的SC ACPA、总分泌型IgA(TSIgA)和IgG ACPA。
症状前个体和RA患者的循环SC ACPA水平与对照组相比显著升高[中位数(四分位间距)分别为108(108)、179(248)和12.5(537)AU/ml;P<0.001],RA患者的SC ACPA水平与症状前个体相比显著升高(P<0.001)。SC ACPA在水平和阳性样本比例方面均随着接近症状发作和诊断而增加。在提前期或诊断后,TSIgA与对照组相比均未升高。最早检测到的SC ACPA阳性样本在症状发作前9年,而IgG ACPA为11年。只有两份提前期样本SC ACPA阳性而IgG ACPA阴性。
在一部分RA患者疾病发展的无症状阶段,循环SC ACPA反应出现并放大。这表明在症状发作和随后的关节炎之前存在黏膜受累。然而,从循环情况来看,SC ACPA似乎并不先于IgG ACPA反应出现。