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成纤维样滑膜细胞靶向抗体与类风湿关节炎一线治疗后早期和持续缓解或低疾病活动度失败相关。

Fibroblast-like synoviocyte targeting antibodies are associated with failure to reach early and sustained remission or low disease activity after first-line therapy in rheumatoid arthritis.

机构信息

Department of Immunology and Infection, Biomedical Research Institute, UHasselt, Hasselt, Belgium.

Expertise Centre for Digital Media Transnational University Limburg, UHasselt, Hasselt, Belgium.

出版信息

RMD Open. 2024 Nov 17;10(4):e004743. doi: 10.1136/rmdopen-2024-004743.

Abstract

OBJECTIVE

To discover antibody biomarkers that can predict a lack of response to first-line therapy in rheumatoid arthritis (RA) patients.

METHODS

Two RA cDNA phage display libraries were screened for novel antibodies in baseline RA sera from the Care in early RA (CareRA) trial, differentiating between patients who did or did not reach remission after first-line therapy (n=20 each). Antibody reactivity to identified University Hasselt (UH)-RA antigens was validated in baseline samples from 136 additional CareRA participants. The novel antibodies' potential to predict failure to reach remission or low disease activity (LDA), according to the Disease Activity Score 28-joint C-reactive protein/erythrocyte sedimentation rate (DAS28CRP/ESR) and Clinical/Simplified Disease Activity Index (CDAI/SDAI), was studied by multivariate analyses. The presence of the antibody targets in RA synovial tissue and the fibroblast-like synoviocyte (FLS) cell line SW982 was determined by immunofluorescence.

RESULTS

We identified antibodies to 41 novel antigens. Antibodies against any of three antigens, UH-RA.305/318/329, discriminated between RA patients not reaching week (w)8 DAS28CRP remission and those that did (36% vs 13%,p=0.0031). In all patients, anti-UH-RA.305/318/329 antibody reactivity was associated with failure to reach week 8 DAS28CRP and DAS28ESR remission (OR 3.63,p=0.0031; OR 2.92,p=0.016; respectively), SDAI/CDAI sustained remission (OR 5.59,p=0.039 for both) and DAS28CRP and DAS28ESR sustained LDA (OR 3.7,p=0.009; OR 2.76,p=0.042; respectively). In rheumatoid factor/anti-citrullinated protein antibody (RF/ACPA) seronegative patients, these antibodies were strongly associated with failure to achieve week 8 DAS28CRP remission (OR 17.3,p=0.0029). Anti-UH-RA.305/329 antibodies were shown to target FLS in RA synovial tissue and SW982 cells.

CONCLUSION

We identified three antibody biomarkers that are associated with failure to achieve remission/LDA after first-line RA therapy.

摘要

目的

发现能够预测类风湿关节炎(RA)患者对一线治疗无反应的抗体生物标志物。

方法

在早期 RA 护理(CareRA)试验的基线 RA 血清中,使用两种 RA cDNA 噬菌体展示文库筛选新型抗体,以区分在一线治疗后达到缓解或未达到缓解的患者(每组 20 例)。在来自 136 名额外的 CareRA 参与者的基线样本中,验证了识别出的哈塞尔特大学(UH)-RA 抗原的抗体反应性。使用多元分析研究了根据疾病活动评分 28 关节 C 反应蛋白/红细胞沉降率(DAS28CRP/ESR)和临床/简化疾病活动指数(CDAI/SDAI),新型抗体预测无法达到缓解或低疾病活动度(LDA)的潜力。通过免疫荧光法确定了 RA 滑膜组织和成纤维样滑膜细胞系 SW982 中抗体靶标的存在。

结果

我们鉴定了 41 种新型抗原的抗体。针对 UH-RA.305/318/329 三种抗原中的任何一种的抗体,可以区分未能达到第 8 周 DAS28CRP 缓解的 RA 患者和达到缓解的患者(36%比 13%,p=0.0031)。在所有患者中,抗 UH-RA.305/318/329 抗体反应与未能达到第 8 周 DAS28CRP 和 DAS28ESR 缓解有关(OR 3.63,p=0.0031;OR 2.92,p=0.016;分别),SDAI/CDAI 持续缓解(OR 5.59,p=0.039,均)和 DAS28CRP 和 DAS28ESR 持续 LDA(OR 3.7,p=0.009;OR 2.76,p=0.042;分别)。在类风湿因子/抗瓜氨酸蛋白抗体(RF/ACPA)阴性患者中,这些抗体与未能达到第 8 周 DAS28CRP 缓解显著相关(OR 17.3,p=0.0029)。抗 UH-RA.305/329 抗体被证明靶向 RA 滑膜组织和 SW982 细胞中的成纤维样滑膜细胞。

结论

我们确定了三种与一线 RA 治疗后无法达到缓解/LDA 相关的抗体生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1d2/11574395/76ee20e90111/rmdopen-10-4-g001.jpg

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