IL-1 Receptor Antagonist (IL-1RA) Gene Polymorphism in Sjogren's Syndrome and Rheumatoid Arthritis

S. Perrier , C. Coussediere , J.J. Dubost , E. Albuisson , B. Sauvezie
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引用次数: 115

Abstract

The gene encoding interleukin-1 receptor antagonist (IL-1ra) has a variable allelic polymorphism. The IL1RN*2 allele was recently described as a factor of severity in several autoimmune diseases and was paradoxically associated with increased production of IL-1ra by monocytesin vitro.We studied this polymorphism in 36 patients with possible or definite primary Sjogren's syndrome and found that IL1RN*2 was significantly more frequent in the definite than in the possible form. In rheumatoid arthritis, the frequency of the allele was not different from that of controls. The serum levels of IL-1ra were markedly higher in Sjogren patients than in those of healthy subjects. By contrast, the salivary IL-1ra levels were decreased. Patients with the allele generally had lower salivary levels and higher serum levels than patients without the allele. In the group of patients with the definite syndrome, CRP and TGF-β1, twoin vitrostimulators of IL-1ra production, were correlated with IL-1ra serum levels. Our results suggest that IL1RN*2 is a marker of more severe forms of Sjogren's syndrome. Its effect on salivary and serum IL-1ra may be distinct, suggesting separate regulatory mechanisms.

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IL-1受体拮抗剂(IL-1RA)基因多态性在干燥综合征和类风湿性关节炎中的作用
编码白介素-1受体拮抗剂(IL-1ra)的基因具有可变的等位基因多态性。IL1RN*2等位基因最近被描述为几种自身免疫性疾病的一个严重因素,并且与单核细胞球蛋白体外产生IL-1ra的增加矛盾地相关。我们在36例可能或明确原发性干燥综合征患者中研究了这种多态性,发现IL1RN*2在明确形式中比在可能形式中明显更频繁。在类风湿关节炎中,该等位基因的频率与对照组没有差异。干燥患者血清IL-1ra水平明显高于健康人群。相比之下,唾液IL-1ra水平降低。与没有该等位基因的患者相比,携带该等位基因的患者通常唾液水平较低,血清水平较高。在明确综合征患者组,两种促IL-1ra产生的体外刺激因子CRP和TGF-β1与血清IL-1ra水平相关。我们的研究结果表明,IL1RN*2是干燥综合征更严重形式的标志。其对唾液和血清IL-1ra的影响可能不同,提示不同的调节机制。
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