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荚膜组织胞浆菌病中干扰素-γ和白细胞介素-4 单核苷酸基因多态性。

Interferon-gamma and interleukin-4 single nucleotide gene polymorphisms in Paracoccidioidomycosis.

机构信息

Departamento de Bioquímica e Imunologia do Instituto de Ciências Biológicas, UFMG, Caixa Postal 486, CEP 31.270-901, Belo Horizonte, MG, Brazil.

出版信息

Cytokine. 2009 Dec;48(3):212-7. doi: 10.1016/j.cyto.2009.07.011. Epub 2009 Aug 13.

Abstract

The gene polymorphisms interferon-gamma (IFN-gamma) +874 T/A and interleukin (IL)-4 -590 C/T have been associated with the altered production of cytokines. Therefore, they might be indicative of the occurrence of Paracoccidioidomycosis (PCM) caused by Paracoccidioides brasiliensis. The analysis of single nucleotide polymorphism (SNP) at position+874 IFN-gamma showed an increase occurrence of A/T genotype in both PCM patients and healthy individuals as control (HIC) (56% and 45%, respectively), while the allelic distribution showed 82% of A allele in the patients and 80% in the controls. The SNP of -590 IL-4 showed that C/T genotype was significantly (p<0.05) more prevalent (39%) in PCM group compared to the HIC group (19%), while IL-4 C/C genotype was significantly less frequent (59%) in the patient group compared to the control group (81%). Otherwise, 41% of PCM patients and 19% of HIC individuals carried the IL-4 T allele. Stimulation of peripheral blood mononuclear cells (PBMC) from PCM patients with cell extract antigenic preparations (PbAg) as well as secreted and surface antigens (MEXO) of P. brasiliensis evidenced that there is no difference in the IFN-gamma production related to A and T alleles between PCM and HIC individuals. However, with IL-4 production, PCM patients classified as C phenotype showed two times more IL-4 production than PCM patients classified as T phenotype and HIC controls. In conclusion, our results suggest that functional genetic variants in the IL-4 promoter could influence the production of IL-4 in PCM.

摘要

干扰素-γ(IFN-γ)+874 T/A 和白细胞介素(IL)-4 -590 C/T 基因多态性与细胞因子产生的改变有关。因此,它们可能是巴西副球孢子菌引起的副球孢子菌病(PCM)发生的指标。IFN-γ+874 位置单核苷酸多态性(SNP)分析显示,PCM 患者和健康对照者(HIC)中 A/T 基因型的发生率均增加(分别为 56%和 45%),而等位基因分布显示患者中 A 等位基因的比例为 82%,对照组中为 80%。-590IL-4 SNP 显示,与 HIC 组(19%)相比,PCM 组 C/T 基因型显著(p<0.05)更为常见(39%),而患者组 IL-4 C/C 基因型明显较少(59%),对照组(81%)。相反,41%的 PCM 患者和 19%的 HIC 个体携带 IL-4 T 等位基因。用细胞提取物抗原制剂(PbAg)以及巴西副球孢子菌的分泌和表面抗原(MEXO)刺激 PCM 患者的外周血单核细胞(PBMC),结果表明 PCM 患者和 HIC 个体的 A 和 T 等位基因与 IFN-γ的产生没有差异。然而,对于 IL-4 的产生,被分类为 C 表型的 PCM 患者的 IL-4 产生量是被分类为 T 表型的 PCM 患者和 HIC 对照者的两倍。总之,我们的结果表明,IL-4 启动子中的功能性遗传变异可能影响 PCM 中 IL-4 的产生。

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