Fabris Martina, Tolusso Barbara, Di Poi Emma, Tomietto Paola, Sacco Stefania, Gremese Elisa, Ferraccioli Gianfranco
Department of Rheumatology, Universita' Cattolica del Sacro Cuore School of Medicine, Rome, Italy.
J Rheumatol. 2005 Jun;32(6):998-1005.
To analyze tumor necrosis factor-alpha (TNF-alpha) synthesis by mononuclear cells stimulated with lipopolysaccharide (LPS) in patients with rheumatoid arthritis (RA).
TNF-alpha molecular expression and extracellular release were assessed in the peripheral blood mononuclear cells (PBMC) of 27 RA patients and 16 healthy blood donor controls during 8 hours of LPS stimulation. We also analyzed the mRNA expression of tristetraprolin (TTP), the major TNF-alpha mRNA destabilizing factor. TNF receptor p75 (TNFR 2) plasma concentrations were also tested in all patients.
Controls and patients demonstrated a comparable wide range of TNF-alpha release capability, but patients achieved the peak value of protein release more quickly. Defining the median TNF-alpha release in controls as the cutoff value to distinguish high and low LPS-induced TNF-alpha-releasing phenotypes, patients with early RA (disease duration < 1 yr) belonged mainly to the low TNF-alpha producer subgroup, whereas patients with long-standing RA (> 1 yr) were prevalently high TNF-alpha producers. TTP molecular expression was higher in patients with shorter, than in patients with longer, disease duration. The profile of TNF-alpha release in patients with early RA changed significantly when retested after 6 months of therapy, while patients with long-standing disease maintained the same behavior as at baseline. Finally, a baseline low TNF-alpha-producer phenotype predisposed to a better responsiveness to disease modifying antirheumatic drugs.
The LPS-induced TNF-alpha-releasing phenotype differs between cells obtained from RA patients with different disease durations and seems to influence the therapeutic outcome.
分析类风湿关节炎(RA)患者中脂多糖(LPS)刺激下单核细胞的肿瘤坏死因子-α(TNF-α)合成情况。
在LPS刺激8小时期间,评估27例RA患者和16例健康献血者对照的外周血单核细胞(PBMC)中TNF-α的分子表达和细胞外释放。我们还分析了主要的TNF-α mRNA去稳定因子锌指蛋白36(TTP)的mRNA表达。所有患者均检测了血浆中TNF受体p75(TNFR 2)的浓度。
对照组和患者表现出相当广泛的TNF-α释放能力,但患者达到蛋白质释放峰值的速度更快。将对照组中TNF-α释放的中位数定义为区分高和低LPS诱导的TNF-α释放表型的临界值,早期RA(病程<1年)患者主要属于低TNF-α产生亚组,而病程较长(>1年)的RA患者大多是高TNF-α产生者。病程较短的患者TTP分子表达高于病程较长的患者。早期RA患者在治疗6个月后重新检测时,TNF-α释放情况发生了显著变化,而病程较长的患者维持了与基线相同的表现。最后,基线低TNF-α产生表型的患者对改善病情抗风湿药物的反应性更好。
LPS诱导的TNF-α释放表型在不同病程的RA患者的细胞之间存在差异,并且似乎影响治疗结果。