Anton P A, Targan S R, Vigna S R, Durham M, Schwabe A D, Shanahan F
Department of Medicine, UCLA 90024.
J Clin Immunol. 1988 Mar;8(2):148-56. doi: 10.1007/BF00917903.
Familial Mediterranean Fever is a disorder of unknown cause characterized by recurrent, self-limited paroxysms of serosal inflammation. Although the neutrophil is the predominant cell involved, no cellular abnormalities are known. Chemiluminescence was studied in neutrophils from 20 asymptomatic patients with this disease and 21 healthy controls to evaluate the oxidative response to formyl-methionyl-leucyl-phenylalanine (f-met-leu-phe). In a subset of patients with familial Mediterranean fever, neutrophils but not monocytes were shown to have significantly enhanced chemiluminescence compared to controls. The enhanced responsiveness of neutrophils to f-met-leu-phe in this disease was found to occur at a postreceptor level. Receptor binding assays demonstrated no differences in binding affinity and receptor number between patients and controls. In addition, a similar enhancement in chemiluminescence was observed with an alternative stimulus (zymosan). In contrast to chemiluminescence, chemotaxis induced by f-met-leu-phe was not enhanced in patients with familial Mediterranean fever. The enhanced neutrophil chemiluminescence may identify a subclinical inflammatory state in attack-free patients with familial Mediterranean fever, as enhanced chemiluminescence is also observed in chronic inflammatory diseases with active inflammation.
家族性地中海热是一种病因不明的疾病,其特征为浆膜炎症反复发作且具有自限性。尽管中性粒细胞是主要受累细胞,但目前尚未发现细胞异常。对20例无症状的该疾病患者和21名健康对照者的中性粒细胞进行化学发光研究,以评估对甲酰甲硫氨酰亮氨酰苯丙氨酸(f-met-leu-phe)的氧化反应。在一部分家族性地中海热患者中,与对照组相比,中性粒细胞而非单核细胞显示出显著增强的化学发光。发现在该疾病中,中性粒细胞对f-met-leu-phe的反应性增强发生在受体后水平。受体结合试验表明患者与对照组之间在结合亲和力和受体数量上没有差异。此外,用另一种刺激物(酵母聚糖)也观察到类似的化学发光增强。与化学发光不同,家族性地中海热患者中f-met-leu-phe诱导的趋化性并未增强。中性粒细胞化学发光增强可能表明无发作的家族性地中海热患者存在亚临床炎症状态,因为在有活动性炎症的慢性炎症性疾病中也观察到化学发光增强。