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Th2细胞因子基因型与一种较轻型的原发性干燥综合征相关。

Th2 cytokine genotypes are associated with a milder form of primary Sjogren's syndrome.

作者信息

Pertovaara M, Antonen J, Hurme M

机构信息

Department of Internal Medicine, Section of Rheumatology, Tampere University Hospital, PO Box 2000, FIN-33521 Tampere, Finland.

出版信息

Ann Rheum Dis. 2006 May;65(5):666-70. doi: 10.1136/ard.2005.040956. Epub 2005 Sep 15.

Abstract

BACKGROUND

Immunohistological studies on salivary and lacrimal glands have yielded conflicting results on the Th1/Th2 balance in primary Sjögren's syndrome (pSS).

OBJECTIVE

To establish whether pSS is a Th1 or Th2 directed autoimmune disease by analysing the polymorphism of the genes encoding for cytokines involved in the regulation of Th1/Th2 differentiation.

METHODS

The polymorphisms of the genes encoding for interleukin 4 (IL4) -590 C/T, interleukin 13 (IL13) +2044 G/A, and interferon gamma (IFNG) +874 T/A were analysed in 63 white Finnish patients with pSS (61 female, two male) and in 63 healthy controls. The clinical and immunological data on the pSS patients were analysed in relation to these cytokine gene polymorphisms.

RESULTS

There were no significant differences in the genotype or allele frequencies of IL4 -590, IL13 +2044, or IFNG +874 between pSS patients and controls. The erythrocyte sedimentation rate and concentrations of serum IgA and serum beta2 microglobulin were lower in pSS patients carrying the IL4 -590 T allele or the IL13 +2044 A allele than in those not carrying the respective alleles. The IL4 -509 T allele and IL13 +2044 A allele carriers less often had purpura than the corresponding non-carriers.

CONCLUSIONS

The frequencies of the cytokine genotypes regulating Th1/Th2 differentiation did not differ between pSS patients and controls. However, the presence of cytokine genotypes with increased susceptibility to atopic and other Th2 diseases was associated with signs of a milder form of pSS. This finding would favour a hypothesis envisaging pSS as primarily a Th1 mediated autoimmune disease.

摘要

背景

关于唾液腺和泪腺的免疫组织学研究在原发性干燥综合征(pSS)的Th1/Th2平衡方面得出了相互矛盾的结果。

目的

通过分析参与Th1/Th2分化调节的细胞因子编码基因的多态性,确定pSS是Th1还是Th2主导的自身免疫性疾病。

方法

对63例芬兰白人pSS患者(61例女性,2例男性)和63例健康对照者分析白细胞介素4(IL4)-590 C/T、白细胞介素13(IL13)+2044 G/A和干扰素γ(IFNG)+874 T/A编码基因的多态性。分析pSS患者的临床和免疫学数据与这些细胞因子基因多态性的关系。

结果

pSS患者与对照组之间IL4 -590、IL13 +2044或IFNG +874的基因型或等位基因频率无显著差异。携带IL4 -590 T等位基因或IL13 +2044 A等位基因的pSS患者的红细胞沉降率、血清IgA和血清β2微球蛋白浓度低于未携带相应等位基因的患者。携带IL4 -509 T等位基因和IL13 +2044 A等位基因的患者紫癜发生率低于相应的非携带者。

结论

pSS患者与对照组之间调节Th1/Th2分化的细胞因子基因型频率无差异。然而,对特应性和其他Th2疾病易感性增加的细胞因子基因型的存在与较轻形式pSS的体征相关。这一发现支持将pSS设想为主要是Th1介导的自身免疫性疾病的假说。

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