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基于质谱的关节炎患者脑脊液分析-TNF 阻断治疗影响的免疫相关候选蛋白。

Mass spectrometry-based analysis of cerebrospinal fluid from arthritis patients-immune-related candidate proteins affected by TNF blocking treatment.

机构信息

Rheumatology Unit, Department of Medicine, Solna, Center of Molecular Medicine (CMM), Karolinska Institutet, Karolinska University Hospital, SE-17176, Stockholm, Sweden.

Neuroimmunology Unit, Department of Clinical Neuroscience, Center of Molecular Medicine (CMM), Karolinska Institutet, Karolinska University Hospital, SE-17176, Stockholm, Sweden.

出版信息

Arthritis Res Ther. 2019 Feb 15;21(1):60. doi: 10.1186/s13075-019-1846-6.

Abstract

BACKGROUND

Signs of inflammation in cerebrospinal fluid (CSF) of rheumatoid arthritis patients correlate positively with fatigue, a central nervous system (CNS)-related symptom that can be partially suppressed by TNF blockade. This suggests a possible role for CNS inflammation in arthritis that may be affected by TNF blockade. We therefore investigated the effects of TNF blockade on the arthritis CSF proteome and how candidate proteins related to clinical measures of disease activity and inflammation.

METHODS

Mass spectrometry-based quantitative proteomic analysis was performed on CSF from seven polyarthritis patients before and during infliximab treatment. Treatment-associated proteins were identified using univariate (Wilcoxon signed rank test) and multivariate (partial least squares discriminant analysis (PLS-DA)) strategies. Relations between selected candidate proteins and clinical measures were investigated using the Spearman correlations. Additionally, selected proteins were cross-referenced to other studies investigating human CSF in a thorough literature search to ensure feasibility of our results.

RESULTS

Univariate analysis of arthritis CSF proteome revealed a decrease of 35 proteins, predominantly involved in inflammatory processes, following TNF blockade. Seven candidate proteins, Contactin-1 (CNTN1), fibrinogen gamma chain (FGG), hemopexin (HPX), cell adhesion molecule-3 (CADM3), alpha-1B-glycoprotein (A1BG), complement factor B (CFB), and beta-2-microglobulin (B2M), were selected for further studies based on identification by both univariate and multivariate analyses and reported detection in human CSF and known associations to arthritis. Decreased levels of FGG and CFB in CSF after treatment showed strong correlations with both erythrocyte sedimentation rate and disability scores, while CNTN1 and CADM3 were associated with pain.

CONCLUSION

Several immune-related proteins in the CSF of arthritis patients decreased during TNF blockade, including FGG and CFB that both correlated strongly with systemic inflammation. Our findings stress that also intrathecal inflammatory pathways are related to arthritis symptoms and may be affected by TNF blockade.

摘要

背景

类风湿关节炎患者脑脊液(CSF)中的炎症迹象与疲劳呈正相关,疲劳是一种与中枢神经系统(CNS)相关的症状,可部分被 TNF 阻断抑制。这表明 CNS 炎症在关节炎中可能起作用,并可能受到 TNF 阻断的影响。因此,我们研究了 TNF 阻断对关节炎 CSF 蛋白质组的影响,以及与疾病活动和炎症的临床测量相关的候选蛋白。

方法

对 7 例多关节炎患者在使用英夫利昔单抗治疗前后的 CSF 进行基于质谱的定量蛋白质组学分析。使用单变量(Wilcoxon 符号秩检验)和多变量(偏最小二乘判别分析(PLS-DA))策略鉴定治疗相关蛋白。使用 Spearman 相关分析研究选定候选蛋白与临床指标之间的关系。此外,通过全面的文献检索,将选定的蛋白与其他研究人类 CSF 的研究进行交叉参考,以确保我们的结果具有可行性。

结果

关节炎 CSF 蛋白质组的单变量分析显示,TNF 阻断后,35 种主要参与炎症过程的蛋白质减少。根据单变量和多变量分析的鉴定,选择了 7 种候选蛋白,包括神经细胞黏附分子 1(CNTN1)、纤维蛋白原 γ 链(FGG)、血红素结合蛋白(HPX)、细胞黏附分子 3(CADM3)、α-1B-糖蛋白(A1BG)、补体因子 B(CFB)和β-2-微球蛋白(B2M),用于进一步研究。这七种蛋白在人类 CSF 中均有报道,并与关节炎有已知关联。治疗后 CSF 中 FGG 和 CFB 的水平降低与红细胞沉降率和残疾评分均呈强相关性,而 CNTN1 和 CADM3 与疼痛相关。

结论

在 TNF 阻断期间,关节炎患者的 CSF 中几种免疫相关蛋白减少,包括与全身炎症密切相关的 FGG 和 CFB。我们的发现强调了鞘内炎症途径与关节炎症状有关,并且可能受到 TNF 阻断的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/6377734/f19d01211df9/13075_2019_1846_Fig1_HTML.jpg

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