Buondonno Ilaria, Rovera Guido, Sassi Francesca, Rigoni Micol Maria, Lomater Claudia, Parisi Simone, Pellerito Raffaele, Isaia Giovanni Carlo, D'Amelio Patrizia
Department of Medical Science, Gerontology and Bone Metabolic Disease Section, University of Torino, Torino, Italy.
Rheumatology Unit, Ospedale Mauriziano, Torino, Italy.
PLoS One. 2017 Jun 5;12(6):e0178463. doi: 10.1371/journal.pone.0178463. eCollection 2017.
The aim of this study was to evaluate differences in T helper cell sub-types and osteoclast (OCs) precursors in peripheral blood between patients affected by early rheumatoid arthritis (eRA) and healthy controls. The effect of administration of cholecalcipherol on clinical and laboratory parameters was subsequently evaluated, by a parallel, randomized double blind, placebo controlled trial. Thirty nine eRA patients and 31 age-matched controls were enrolled and compared for levels of 25OH vitamin D, T helper cell sub-types, OCs precursors including both classical and non-classical and pro-inflammatory cytokines at baseline. Eligible patients were female ≥18 years of age with a diagnosis of RA, as defined by the American College of Rheumatology 2010 criteria for <6 months prior to inclusion in the study. Patients with auto-immune or inflammatory diseases other than RA were excluded. Patients treated with glucocorticoids (GCs), disease modifying activity drugs and biologic agents within the past 6 months were also excluded. In the second phase of the study, eRA patients were randomly assigned to standard treatment with methotrexate (MTX) and GCs with (21) or without (18) cholecalcipherol (300,000 IU) and followed for 3 months; the randomization was done by computer generated tables to allocate treatments. Three patients didn't come back to the follow up visit for personal reasons. None of the patients experienced adverse events. The main outcome measures were T cells phenotypes, OCs precursors and inflammatory cytokines. Secondary outcome measure were clinical parameters. In eRA, 25OH vitamin D levels were significantly lower. CD4+/IFNγ+,CD4+/IL4+, CD4+/IL17A+ and CD4+IL17A+IFNγ+, cells were increased in eRA as well as non-classical OCs precursors, whereas T regulatory cells were not altered. TNFα, TGFβ1, RANKL, IL-23 and IL-6 were increased in eRA. Non-classical OCs, IL-23 and IL-6 correlated with disease severity and activity. Standard treatment with MTX and GC ameliorated clinical symptoms and reduced IL-23, whereas it did not affect CD4+ cells sub-sets nor OCs precursors. After 3 months, the combined use of cholecalcipherol significantly ameliorated the effect of treatment on global health. In eRA, a significant imbalance in T CD4+ sub-types accompanied by increased levels of non-classical OCs precursors and pro-inflammatory cytokines was observed. A single dose of cholecalcipherol (300,000 IU) combined with standard treatment significantly ameliorates patients general health.
本研究旨在评估早期类风湿关节炎(eRA)患者与健康对照者外周血中辅助性T细胞亚群和破骨细胞(OCs)前体的差异。随后,通过一项平行、随机双盲、安慰剂对照试验,评估了胆钙化醇给药对临床和实验室参数的影响。招募了39例eRA患者和31例年龄匹配的对照者,并比较了基线时25OH维生素D水平、辅助性T细胞亚群、包括经典和非经典OCs前体以及促炎细胞因子的水平。符合条件的患者为年龄≥18岁的女性,根据美国风湿病学会2010年标准诊断为类风湿关节炎,纳入研究前病程<6个月。排除患有类风湿关节炎以外的自身免疫性或炎性疾病的患者。过去6个月内接受过糖皮质激素(GCs)、改善病情抗风湿药和生物制剂治疗的患者也被排除。在研究的第二阶段,eRA患者被随机分配接受甲氨蝶呤(MTX)和GCs的标准治疗,其中21例联合胆钙化醇(300,000 IU),18例不联合,随访3个月;随机分组通过计算机生成的表格进行。3例患者因个人原因未返回进行随访。所有患者均未发生不良事件。主要观察指标为T细胞表型、OCs前体和炎性细胞因子。次要观察指标为临床参数。在eRA患者中,25OH维生素D水平显著降低。eRA患者中CD4+/IFNγ+、CD4+/IL4+、CD4+/IL17A+和CD4+IL17A+IFNγ+细胞以及非经典OCs前体增加,而调节性T细胞未改变。eRA患者中TNFα、TGFβ1、RANKL、IL-23和IL-6升高。非经典OCs、IL-23和IL-6与疾病严重程度和活动度相关。MTX和GCs的标准治疗改善了临床症状并降低了IL-23水平,但未影响CD4+细胞亚群和OCs前体。3个月后,联合使用胆钙化醇显著改善了治疗对整体健康的效果。在eRA患者中,观察到CD4+T细胞亚群存在显著失衡,同时非经典OCs前体和促炎细胞因子水平升高。单剂量胆钙化醇(300,000 IU)联合标准治疗显著改善了患者的总体健康状况。