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青少年特发性关节炎患者的部分C4缺乏症

Partial C4 deficiency in juvenile idiopathic arthritis patients.

作者信息

Gilliam Brooke E, Wolff Anne E, Moore Terry L

机构信息

Division of Rheumatology, Saint Louis University School of Medicine, 1402 South Grand Boulevard, Saint Louis, MO 63104, USA.

出版信息

J Clin Rheumatol. 2007 Oct;13(5):256-60. doi: 10.1097/RHU.0b013e318156b9e3.

Abstract

OBJECTIVES

C4 is encoded by 2 distinct but closely linked loci within the major histocompatibility complex locus on human chromosome 6. C4A deficiencies have been associated with autoimmune disease and C4B with increased frequency of infection. C4 deficiencies have rarely been associated with juvenile idiopathic arthritis (JIA). Our aim was to investigate the prevalence of deficiencies in C4 allotypes in JIA patients.

METHODS

We evaluated 61 patients [35 JIA patients, 15 systemic lupus erythematosus patients, 9 rheumatoid arthritis patients, and 2 mixed connective tissue disease (CTD) patients] for C4 deficiency. Genomic DNA was isolated from whole blood and subjected to polymerase chain reaction using sequence-specific primers for C4 allotypes.

RESULTS

We found 5 JIA patients with C4 deficiencies. Two IgM rheumatoid factor-positive JIA polyarthritis patients had C4 deficiencies, one with complete C4A deficiency and another with partial C4A and complete C4B deficiency. Two oligoarthritis patients displayed partial C4B deficiencies, and complete C4B deficiency was revealed in 1 IgM rheumatoid factor-negative polyarthritis patient. Three patients had histories of recurrent infections and 2 demonstrated a more severe disease course. Disease controls showed 8 systemic lupus erythematosus patients had partial C4 deficiencies, whereas no deficiencies were revealed in the rheumatoid arthritis or mixed CTD patients.

CONCLUSIONS

Defects in the complement system have been implicated in the pathogenesis of CTD. However, the specific role of C4 in JIA is not clear. We demonstrate partial C4 deficiencies in 5 JIA patients. Our findings suggest an association between C4 deficiency and another CTD, JIA, as well as with disease severity and recurrent infections.

摘要

目的

C4由人类6号染色体主要组织相容性复合体基因座内2个不同但紧密连锁的基因座编码。C4A缺陷与自身免疫性疾病相关,C4B缺陷与感染频率增加相关。C4缺陷很少与幼年特发性关节炎(JIA)相关。我们的目的是调查JIA患者中C4同种异型缺陷的患病率。

方法

我们评估了61例患者[35例JIA患者、15例系统性红斑狼疮患者、9例类风湿关节炎患者和2例混合性结缔组织病(CTD)患者]的C4缺陷情况。从全血中分离基因组DNA,并使用针对C4同种异型的序列特异性引物进行聚合酶链反应。

结果

我们发现5例JIA患者存在C4缺陷。2例IgM类风湿因子阳性的JIA多关节炎患者存在C4缺陷,1例完全C4A缺陷,另1例部分C4A和完全C4B缺陷。2例少关节炎患者表现为部分C4B缺陷,1例IgM类风湿因子阴性的多关节炎患者存在完全C4B缺陷。3例患者有反复感染史,2例病情较重。疾病对照组中,8例系统性红斑狼疮患者存在部分C4缺陷,而类风湿关节炎或混合性CTD患者未发现缺陷。

结论

补体系统缺陷与CTD的发病机制有关。然而,C4在JIA中的具体作用尚不清楚。我们在5例JIA患者中发现了部分C4缺陷。我们的研究结果表明C4缺陷与另一种CTD即JIA之间存在关联,同时也与疾病严重程度和反复感染有关。

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