Szeremeta Anna, Jura-Półtorak Agnieszka, Zoń-Giebel Aleksandra, Olczyk Krystyna, Komosińska-Vassev Katarzyna
Department of Clinical Chemistry and Laboratory Diagnostics, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Jedności 8, 41-200 Sosnowiec, Poland.
Department of Rheumatology and Rehabilitation, Specialty Hospital No. 1, Żeromskiego 7, 41-902 Bytom, Poland.
J Clin Med. 2022 Jul 20;11(14):4213. doi: 10.3390/jcm11144213.
Sulfated glycosaminoglycans (sGAGs) are likely to play an important role in the development and progression of rheumatoid arthritis (RA)-associated atherosclerosis. The present study investigated the effect of anti-tumor necrosis factor-α (anti-TNF-α) therapy in combination with methotrexate on plasma sGAG levels and serum markers of endothelial dysfunction. Among sGAG types, plasma chondroitin/dermatan sulfate (CS/DS) and heparan sulfate/heparin (HS/H) were characterized using electrophoretic fractionation. Serum levels of soluble vascular cell adhesion molecule-1 (sVCAM-1), monocyte chemoattractant protein-1 (MCP-1), matrix metalloproteinase-9 (MMP-9) and asymmetric dimethylarginine (ADMA) were measured by immunoassays. The measurements were carried out four times: at baseline and after 3, 9 and 15 months of anti-TNF-α therapy. All analyzed parameters, excluding ADMA, were significantly elevated in patients with RA before the implementation of biological therapy compared to healthy subjects. Performed anti-TNF-α treatment led to a successive decrease in HS/H levels toward normal values, without any effect on CS/DS levels in female RA patients. The treatment was also effective at lowering the serum levels of sVCAM-1, MCP-1, MMP-9 and ADMA. Moreover, a significant positive correlation was found between the circulating HS/H and the 28 joint disease activity score based on the erythrocyte sedimentation rate (DAS28-ESR, r = 0.408; p <0.05), MCP-1 (r = 0.398; p <0.05) and ADMA (r = 0.396; p <0.05) in patients before the first dose of TNF-α inhibitor. In conclusion, a beneficial effect of anti-TNF-α therapy on cell-surface heparan sulfate proteoglycans (HSPGs)/HS turnover and endothelial dysfunction was observed in this study. This was manifested by a decrease in blood HS/H levels and markers of endothelial activation, respectively. Moreover, the decrease in the concentration of HS/H in the blood of patients during treatment, progressing with the decline in disease activity, indicates that the plasma HS/H profile may be useful for monitoring the efficacy of anti-TNF-α treatment in patients with RA.
硫酸化糖胺聚糖(sGAGs)可能在类风湿关节炎(RA)相关动脉粥样硬化的发生和发展中起重要作用。本研究调查了抗肿瘤坏死因子-α(抗TNF-α)疗法联合甲氨蝶呤对血浆sGAG水平和内皮功能障碍血清标志物的影响。在sGAG类型中,使用电泳分级法对血浆软骨素/硫酸皮肤素(CS/DS)和硫酸乙酰肝素/肝素(HS/H)进行了表征。通过免疫测定法测量血清可溶性血管细胞粘附分子-1(sVCAM-1)、单核细胞趋化蛋白-1(MCP-1)、基质金属蛋白酶-9(MMP-9)和不对称二甲基精氨酸(ADMA)的水平。测量进行了四次:在基线时以及抗TNF-α治疗3、9和15个月后。与健康受试者相比,在实施生物治疗前,RA患者中所有分析参数(不包括ADMA)均显著升高。进行的抗TNF-α治疗导致女性RA患者的HS/H水平连续下降至正常水平,而对CS/DS水平没有任何影响。该治疗在降低sVCAM-1、MCP-1、MMP-9和ADMA的血清水平方面也有效。此外,在首次给予TNF-α抑制剂之前,患者的循环HS/H与基于红细胞沉降率的28关节疾病活动评分(DAS28-ESR,r = 0.408;p <0.05)、MCP-1(r = 0.398;p <0.05)和ADMA(r = 0.396;p <0.05)之间存在显著正相关。总之,本研究观察到抗TNF-α疗法对细胞表面硫酸乙酰肝素蛋白聚糖(HSPGs)/HS周转和内皮功能障碍具有有益作用。这分别表现为血液HS/H水平和内皮激活标志物的降低。此外,治疗期间患者血液中HS/H浓度的降低随着疾病活动度的下降而进展,表明血浆HS/H谱可能有助于监测RA患者抗TNF-α治疗的疗效。