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中国特发性血小板减少性紫癜患者中干扰素-γ +874A/T和白细胞介素-4内含子3 VNTR基因多态性

Interferon-gamma +874A/T and interleukin-4 intron3 VNTR gene polymorphisms in Chinese patients with idiopathic thrombocytopenic purpura.

作者信息

Chen Xiaoli, Xu Jianhui, Chen Zhenping, Zhou Zeping, Feng Xiaoming, Zhou Yuling, Ren Qian, Yang Renchi, Han Zhong Chao

机构信息

State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.

出版信息

Eur J Haematol. 2007 Sep;79(3):191-7. doi: 10.1111/j.1600-0609.2007.00914.x. Epub 2007 Jul 26.

Abstract

OBJECTIVES

The polarization of Th1/Th2 towards Th1 contributes to the pathogenesis of idiopathic thrombocytopenic purpura (ITP). Cytokines may play crucial roles in the pathogenesis of ITP. The purpose of this study was to investigate whether the interferon (IFN)-gamma +874(A/T) and interleukin-4 (IL-4) variable number of tandem repeats (VNTR) in intron3 polymorphisms may be responsible in part for genetic susceptibility to ITP.

METHODS

Genotyping of IFN-gamma +874A/T and IL-4 intron3 VNTR was performed in 196 patients with ITP and 128 healthy individuals by polymerase chain reaction sequence-specific primers and direct PCR respectively.

RESULTS

There was no association between IFN-gamma +874A/T and IL-4 intron3 VNTR polymorphism and ITP risk when all patients, as a group, were analyzed. When the patients were subdivided into two groups: childhood ITP and adult ITP, no statistical differences were found in the genotype and allele frequencies of IFN-gamma +874A/T and IL-4 intron3 VNTR between the two groups and the controls. Similar results were observed between acute childhood ITP, chronic childhood ITP, acute adult ITP or chronic adult ITP and the controls.

CONCLUSION

These polymorphisms were distributed similarly between the patients with ITP and the controls, demonstrating that these two candidate gene polymorphisms are not attributed to ITP susceptibility.

摘要

目的

Th1/Th2向Th1极化有助于特发性血小板减少性紫癜(ITP)的发病机制。细胞因子可能在ITP发病机制中起关键作用。本研究的目的是调查干扰素(IFN)-γ +874(A/T)和白细胞介素-4(IL-4)第3内含子串联重复序列(VNTR)多态性是否可能部分导致ITP的遗传易感性。

方法

分别采用聚合酶链反应序列特异性引物和直接PCR对196例ITP患者和128例健康个体进行IFN-γ +874A/T和IL-4第3内含子VNTR基因分型。

结果

将所有患者作为一个整体分析时,IFN-γ +874A/T和IL-4第3内含子VNTR多态性与ITP风险之间无关联。当将患者分为两组:儿童ITP和成人ITP时,两组与对照组之间IFN-γ +874A/T和IL-4第3内含子VNTR的基因型和等位基因频率无统计学差异。在儿童急性ITP、儿童慢性ITP、成人急性ITP或成人慢性ITP与对照组之间观察到类似结果。

结论

这些多态性在ITP患者和对照组之间分布相似,表明这两个候选基因多态性与ITP易感性无关。

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