Coury F, Ferraro-Peyret C, Le Cam S, Guerin S, Tebib J, Sibilia J, Bienvenu J, Fabien N
Department of Rheumatology, Hospices Civils de Lyon; INSERM U 851, Centre Hospitalier Lyon-Sud, Pierre Bénite, 69495, France.
Clin Exp Rheumatol. 2008 Mar-Apr;26(2):234-9.
The efficacy of anti-tumour necrosis factor-alpha (TNF-alpha) therapies in rheumatoid arthritis (RA) has been mainly attributed to TNF-alpha neutralisation. Other mechanism as immune cell apoptosis, which is impaired in RA, may also be induced by anti-TNF-alpha therapies. The aim of our study was to investigate whether TNF-alpha inhibitors could induce apoptosis in vitro of the peripheral blood lymphocytes of RA patients.
Peripheral blood mononuclear cells (PBMC) isolated from 24 patients with RA and 18 healthy donors were incubated with anti-TNF-alpha agents, infliximab or etanercept, in comparison with no agent and including an isotypic control, for 48 hours. Apoptosis was detected and quantified by annexin V labelling of phosphatidylserine externalization using cytofluorometric analysis and compared with PBMC production TNF-alpha in vitro.
In healthy donors, induced apoptosis was observed in 0.3% to 3.8% of lymphocytes with both therapies. In RA patients the treatment induced lymphocyte apoptosis in 17 of 24 patients with a percentage of annexin V-positive lymphocytes ranging from 0.1% to 25%. Among these 17 RA patients, a significant in vitro lymphocyte apoptosis (> 4%) was observed in 11 patients (46%) compared with healthy donors (p < 0.01). The variability of the response to anti-TNF-alpha within the RA population was not dependent on TNF-alpha synthesis or disease activity.
In vitro induction of lymphocyte apoptosis by anti-TNF-alpha was observed in a subgroup of RA patients. Based on these data, it would be of interest to further study the interindividual variations of sensitivity to apoptosis induced by TNF alpha inhibitors in relation to treatment efficacy or resistance observed in RA patients.
抗肿瘤坏死因子-α(TNF-α)疗法在类风湿关节炎(RA)中的疗效主要归因于TNF-α的中和作用。其他机制如免疫细胞凋亡,在RA中受损,也可能由抗TNF-α疗法诱导。我们研究的目的是调查TNF-α抑制剂是否能在体外诱导RA患者外周血淋巴细胞凋亡。
从24例RA患者和18名健康供者中分离出外周血单个核细胞(PBMC),与抗TNF-α药物英夫利昔单抗或依那西普一起孵育48小时,同时设置无药物组和同型对照,通过流式细胞术分析用膜联蛋白V标记磷脂酰丝氨酸外化来检测和定量凋亡,并与PBMC体外产生TNF-α的情况进行比较。
在健康供者中,两种疗法均使0.3%至3.8%的淋巴细胞发生凋亡。在RA患者中,治疗使24例患者中的17例淋巴细胞发生凋亡,膜联蛋白V阳性淋巴细胞百分比为0.1%至25%。在这17例RA患者中,与健康供者相比,11例患者(46%)观察到显著的体外淋巴细胞凋亡(>4%)(p<0.01)。RA人群中对抗TNF-α反应的变异性不依赖于TNF-α的合成或疾病活动度。
在一部分RA患者中观察到抗TNF-α在体外诱导淋巴细胞凋亡。基于这些数据,进一步研究TNF-α抑制剂诱导凋亡的敏感性个体差异与RA患者观察到的治疗疗效或耐药性之间的关系将是有意义的。