D'Osualdo Andrea, Ferlito Francesca, Prigione Ignazia, Obici Laura, Meini Antonella, Zulian Francesco, Pontillo Alessandra, Corona Fabrizia, Barcellona Roberto, Di Duca Marco, Santamaria Giuseppe, Traverso Francesco, Picco Paolo, Baldi Maurizia, Plebani Alessandro, Ravazzolo Roberto, Ceccherini Isabella, Martini Alberto, Gattorno Marco
Istituto G. Gaslini, Genoa, Italy.
Arthritis Rheum. 2006 Mar;54(3):998-1008. doi: 10.1002/art.21657.
To explore tumor necrosis factor (TNF)-induced apoptosis in neutrophils from patients with TNF receptor-associated periodic syndrome (TRAPS) and to correlate the results with the different kinds of TNFRSF1A mutations.
Two hundred sixty-five patients with clinically suspected inherited autoinflammatory syndrome were screened for mutations of the TNFRSF1A gene. Neutrophils were isolated from heparinized blood by dextran sedimentation and incubated with and without cycloheximide (CHX) and TNFalpha. Cell apoptosis was assessed by human annexin V binding, and caspase 8 activation was assessed by flow cytometry.
Twenty-one patients were found to carry a variant of the TNFRSF1A gene: 13 patients had an R92Q substitution, and 8 patients presented other missense substitutions, 1 splicing mutation, and 1 in-frame interstitial deletion. Neutrophil stimulation with TNF and CHX was associated with induction of apoptosis in 12 normal controls and in 10 subjects with the R92Q mutation. Conversely, neutrophils from 8 TRAPS patients with mutations of cysteine or threonine residues or interstitial deletion did not show any induction of apoptosis after stimulation. The incidence of the R92Q mutation among patients with recurrent autoinflammatory syndromes was similar to that observed in the normal population.
Resistance to TNF-mediated apoptosis is a feature in TRAPS patients who have mutations of cysteine residues or interstitial deletion, and may play a pathogenic role. The R92Q mutation does not appear to be significantly associated with TRAPS.
探讨肿瘤坏死因子(TNF)诱导肿瘤坏死因子受体相关周期性综合征(TRAPS)患者中性粒细胞凋亡的情况,并将结果与不同类型的TNFRSF1A突变相关联。
对265例临床怀疑为遗传性自身炎症综合征的患者进行TNFRSF1A基因突变筛查。通过葡聚糖沉淀法从肝素化血液中分离中性粒细胞,并在有或无放线菌酮(CHX)和TNFα的情况下进行孵育。通过人膜联蛋白V结合评估细胞凋亡,通过流式细胞术评估半胱天冬酶8激活情况。
发现21例患者携带TNFRSF1A基因变异:13例患者有R92Q替代,8例患者有其他错义替代、1例剪接突变和1例框内间质缺失。用TNF和CHX刺激中性粒细胞可诱导12例正常对照和10例有R92Q突变的受试者发生凋亡。相反,8例有半胱氨酸或苏氨酸残基突变或间质缺失的TRAPS患者的中性粒细胞在刺激后未显示任何凋亡诱导。复发性自身炎症综合征患者中R92Q突变的发生率与正常人群中观察到的相似。
对TNF介导的凋亡产生抗性是有半胱氨酸残基突变或间质缺失的TRAPS患者的一个特征,可能起致病作用。R92Q突变似乎与TRAPS无显著关联。